PEPTIDE SCAFFOLD DESIGN

- Bionor Immuno AS

The present invention relates to novel peptides and methods for treatment, diagnosis and prognosis of virus infections including infections with HCV, HIV, CMV and Influenza. The invention further relates to methods for identifying and providing peptides useful for the treatment and diagnosis.

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Description
FIELD OF THE INVENTION

The present invention relates to novel peptides and methods for treatment, diagnosis and prognosis of virus infections including infections with HCV, HIV, CMV and Influenza. The invention further relates to methods for identifying and providing peptides useful for the treatment and diagnosis.

BACKGROUND OF THE INVENTION

Conventional approaches to vaccine development have implemented either whole replication competent virus which has been attenuated (e.g. Sabin polio vaccine, measles, mumps, rubella (MMR)) or inactivated virions that are not replication competent. On occasions, the inactivated virus vaccines may include split vaccines where the virus particles have been disrupted. Molecular techniques have also been used to develop the subunit vaccine (e.g. hepatitis B vaccine) that consists only of the surface glycoproteins of hepatitis B virus. The inactivated virus vaccines tend to induce primarily antibody responses to the viruses in question, whereas the live attenuated vaccines induce both cell-mediated immunity as well as an antibody response since the vaccine induces a transient infection.

The only disease which has been eliminated by virtue of a successful vaccination campaign is smallpox. A campaign is currently in progress to eradicate polio. Features of virus infections that can be eliminated by vaccination are infections caused by viruses with stable virus antigens (i.e. very low mutation frequency, few subtypes), that lack a reservoir in other animal species, viruses that do not persist in the body once the infection is over and where vaccination leads to long lasting immunity. Viruses such as polio and measles fulfill these criteria whereas viruses such as influenza virus (Flu), HCV, and HIV that vary their protein sequences do not. It is for this reason that new and alternate approaches are required to develop vaccines for these diseases.

Vaccination aims to stimulate the immune response to a specific pathogen in advance of infection. When an individual is exposed to that pathogen, a memory response is triggered which prevents the establishment of infection. Vaccines therefore stimulate the adaptive immune response which unlike innate immunity, is long lived and has memory. There are two major arms to the adaptive immune system. Humoral immunity which involves the development of antibodies that can bind virus particles and certain antibodies that can neutralize infection. Cell mediated immunity that leads to the development of cytotoxic T-cells that kill infected cells exposing viral epitopes in the context of human leukocyte antigen (HLA) class I, in this way eliminating infected cells.

The challenge of providing vaccines suitable for stimulation of the adaptive immune system is that peptide epitopes need to be taken up by the antigen presenting cells.

Several peptides have been demonstrated to translocate across the plasma membrane of eukaryotic cells by a seemingly energy-independent pathway. These peptides are defined as cell-penetrating peptides (CPPs). Cellular delivery using these cell-penetrating peptides offers several advantages over conventional techniques. It is non-invasive, energy-independent, is efficient for a broad range of cell types and can be applied to cells en masse.

Hepatitis means inflammation of the liver which can be caused by a variety of factors including toxins, certain drugs, some diseases, heavy alcohol use, and bacterial and viral infections. Hepatitis is also the name of a family of viral infections that affect the liver; the most common types in the developed world are hepatitis A, hepatitis B, and hepatitis C.

Hepatitis C is a liver disease that results from infection with the hepatitis C virus (HCV). It can range in severity from a mild illness lasting a few weeks to a serious, lifelong illness.

Hepatitis C is spread via blood; the most common form of transmission is through sharing needles or other equipment used to inject drugs. The infection can be either “acute” or “chronic”. Acute HCV infection is an asymptomatic, short-term illness that occurs within the first 6 months after someone is exposed to the hepatitis C virus. For most people, acute infection leads to chronic infection, which can result in long-term complications and even death.

HCV is an enveloped positive stranded ribonucleic acid (RNA) virus with a diameter of about 50 nm, belonging to the genus Hepacivirus in the family Flaviviridae that replicate in the cytoplasm of infected cells. The only known reservoir for HCV is humans, although the virus has experimentally been transmitted to chimpanzees. The natural targets of HCV are hepatocytes and possibly B-lymphocytes. As of 2008, six different genotypes and more than 100 subtypes of the virus are known. Replication occurs through an RNA-dependent RNA polymerase that lacks a proofreading function, which results in a very high rate of mutations. Rapid mutations in a hypervariable region of the HCV genome coding for the envelope proteins enable the virus to escape immune surveillance by the host. As a consequence, most HCV-infected people proceed to chronic infection.

It is estimated that 170 million people are infected with HCV worldwide, equating to approximately 3% of the global population. There are also approximately 3-4 million people who are infected every year; with an estimated 80% of these newly infected patients progressing to chronic infection.

The 6 genotypes of HCV have different geographical spread. The disease in the early stages is generally asymptomatic; the majority of patients with chronic infection eventually progress to complications such as liver fibrosis and cirrhosis, and, in 1-5% of cases, hepatocellular carcinoma.

HCV is the major cause of non-A, non-B hepatitis worldwide. Acute infection with HCV frequently leads to chronic hepatitis and end-stage cirrhosis. It is estimated that up to 20% of HCV chronic carriers may develop cirrhosis over a time period of about 20 years and that of those with cirrhosis between 1 to 4% is at risk to develop liver carcinoma.

The about 9.6 kb single-stranded RNA genome of the HCV virus comprises a 5′- and 3′-noncoding region (NCRs) and, in between these NCRs a single long open reading frame of about 9 kb encoding an HCV polyprotein of about 3000 amino acids.

HCV polypeptides are produced by translation from the open reading frame and cotranslational proteolytic processing. Structural proteins are derived from the amino-terminal one-fourth of the coding region and include the capsid or Core protein (about 21 kDa), the E1 envelope glycoprotein (about 35 kDa) and the E2 envelope glycoprotein (about 70 kDa, previously called NS1), and p7 (about 7 kDa). The E2 protein can occur with or without a C-terminal fusion of the p7 protein (Shimotohno et al. 1995). An alternative open reading frame in the Core-region has been found which is encoding and expressing a protein of about 17 kDa called F (Frameshift) protein (Xu et al. 2001; Ou & Xu in US Patent Application Publication No. US2002/0076415). In the same region, ORFs for other 14-17 kDa ARFPs (Alternative Reading Frame Proteins), A1 to A4, were discovered and antibodies to at least A1, A2 and A3 were detected in sera of chronically infected patients (Walewski et al. 2001). From the remainder of the HCV coding region, the non-structural HCV proteins are derived which include NS2 (about 23 kDa), NS3 (about 70 kDa), NS4A (about 8 kDa), NS4B (about 27 kDa), NS5A (about 58 kDa) and NS5B (about 68 kDa) (Grakoui et al. 1993).

Influenza remains a significant cause of mortality and morbidity worldwide. The World Health Organisation (WHO) estimates that seasonal epidemics affect 3-5 million people with severe illness annually and result in 250,000-500,000 mortalities. Influenza is caused by viruses in the family Orthomyxoviridae which are negative stranded RNA viruses. The influenza virus exists as three types, A, B and C of which only A is associated with pandemics. Types A viruses are found in both humans and animals, particularly birds but also other mammals such as pigs. Type A viruses are further typed into subtypes according to different kinds and combinations of virus surface proteins. Among many subtypes in 2009 influenza A (H1N1) and A (H3N2) subtypes were circulating among humans. Influenza A and B are included in the seasonal vaccine, whereas influenza C occurs only rarely, and so it is not included in the seasonal vaccine. Type B viruses are human specific and Type C viruses cause a very mild disease. The genomes of Orthomyxoviruses are segmented. Influenza viruses Types A and B have 8 segments whereas type C has seven. Pandemics may arise as a result of re-assortment of gene segments when two different type A viruses infect the same cell. There is no immunity in the population to this novel re-assorted virus. Three pandemics occurred in the twentieth century: “Spanish influenza” in 1918, “Asian influenza” in 1957, and “Hong Kong influenza” in 1968. The 1918 pandemic killed an estimated 40-50 million people worldwide. Subsequent pandemics were much milder, with an estimated 2 million deaths in 1957 and 1 million deaths in 1968. In June 2009 the WHO declared a pandemic from influenza virus H1N1 (swine Influenza) which was declared over in August 2010.

Human papillomaviruses are made up of a group of DNA viruses in the family Papillomaviridae which infect the skin and mucous membranes. Two groups which are derived from more than 100 different identified subtypes are the main cause for clinical concern: those causing warts (both benign and genital warts), and a group of 12 “high risk” subtypes that can result in cervical cancer. This latter group has been attributed as a contributory factor in the development of nearly all types of cervical cancer. Worldwide, cervical cancer remains the second most common malignancy in women, and is a leading cause of cancer-related death for females in developing countries. HPV 16 and 18 have been mainly associated with cervical cancer, however, the virus is also a cause of throat cancer in both men and women. HPV is transmitted through contact and enters the skin through abrasions. An abortive infection, where only the early proteins are expressed is associated with cancer development.

OBJECT OF THE INVENTION

It is an object of embodiments of the invention to provide peptides that may be used as immunogens to stimulate an adaptive immune response in a subject.

In particular, it is an object of embodiments of the invention to provide peptides that may be taken up by antigen presenting cells (macrophages and dendritic cells) such that epitopes within the peptides are correctly processed and presented to T-lymphocytes in order to stimulate an effective immune response.

Further, it is an object of embodiments of the invention to provide peptides that may be used as antigens, to provide immunogenic compositions and methods for inducing an immune response in a subject against an antigen.

SUMMARY OF THE INVENTION

The present invention pertains to a peptide design promoting uptake of peptide epitopes by antigen presenting cells (macrophages and dendritic cells) such that the epitopes can be correctly processed and presented in the context of HLA class I and II to stimulate both CD4+ and CD8+ T-lymphocytes. CD8+ T-lymphocytes with cytotoxic capacity will kill infected cells bearing the epitope of interest. CD4+ T-lymphocyte provide ‘help’ to sustain effective CD8+ T-lymphocyte responses.

It has been found by the present inventor(s) that peptide constructs—amino acid sequences with a particular pattern or scaffold design—have the ability to effectively penetrate the cell membrane. Accordingly, the peptide constructs according to the present invention may be used to load cells with an immunogenically effective amount of a peptide or fragments of this peptide that can be presented by macrophages and dendritic cells. Accordingly these peptide constructs may elicit a Cytotoxic T-lymphocyte immune (CTL) response and/or a Humoral Immune Response.

So, in a first aspect the present invention relates to an isolated cell-penetrating peptide of not more than 60 amino acids with the following structure


X1-X2-X3-X4-X5  (formula I),

wherein X1 and X3 independently defines a linear sequence of any 1, 2, 3 or 4 amino acid(s) independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof; X2 defines a linear sequence of 8-30 amino acids derived from an antigen; X4 defines a linear sequence of 8-30 amino acids derived from said antigen, said sequence X4 being different from X2; and wherein X5 is any one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof.

It is to be understood that the amino acid sequence of formula I refers to a peptide sequence in a standard N- to C-terminal direction, wherein the first amino acid mentioned is the N-terminal amino acid that may have an amino (—NH2) group or alternatively an —NH3+ group. The last amino acid mentioned is the C-terminal that may have a free carboxyl group (—COON) or a carboxylate group. In some embodiments the N- and/or C-terminal amino acid is modified, such as by N-terminal acetylation or C-terminal amidation. The symbol “—” used in formula I refers to a standard peptide bond, such as a standard peptide bond between X1 and X2 in “X1-X2”.

It is further to be understood that the peptides according to the invention primarily are intended for synthetic peptide synthesis. However, the peptides may be longer than 60 amino acids, if the peptides are produced by recombinant means. Accordingly, an alternative first aspect or the present invention relates to an isolated cell-penetrating peptide comprising a peptide sequence with the following structure


X1-X2-X3-X4-X5  (formula I),

wherein X1 and X3 independently defines a linear sequence of any 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof; X2 defines a linear sequence of 8-30 amino acids derived from an antigen; X4 defines a linear sequence of 8-30 amino acids derived from said antigen, said sequence X4 being different from X2; and wherein X5 is any one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof.

In a second aspect the present invention relates to an isolated peptide of not more than 60 amino acids comprising a sequence of X2 and/or X4 as independently defined in any one of table 1 or table 2.

In a third aspect the present invention relates to the use of a peptide comprising a sequence of X2 or X4 as independently defined in any one of table 1 or table 2 for inducing an immune response in a subject.

In a further aspect the present invention relates to an isolated peptide consisting of X1-X5 as defined in any one of table 1 or table 2.

In a further aspect the present invention relates to a dimer peptide comprising two peptide monomers, wherein each peptide monomer is according to the invention.

In a further aspect the present invention relates to a peptide combination comprising two or more peptides according to the invention.

In a further aspect the present invention relates to an isolated nucleic acid or polynucleotide encoding a peptide according to the invention.

In a further aspect the present invention relates to a vector comprising the nucleic acid or polynucleotide encoding a peptide according to the invention.

In a further aspect the present invention relates to a host cell comprising the vector comprising the nucleic acid or polynucleotide encoding a peptide according to the invention.

In a further aspect the present invention relates to an immunogenic composition comprising at least one peptide according to the invention, a dimer peptide comprising two peptides monomers, wherein each peptide monomer is according to the invention, a peptide combination comprising two or more peptide according to the invention, the nucleic acid or polynucleotide encoding a peptide according to the invention, or the vector comprising the nucleic acid or polynucleotide encoding a peptide according to the invention; in combination with a pharmaceutically acceptable diluent or vehicle and optionally an immunological adjuvant.

In a further aspect the present invention relates to a method for inducing an immune response in a subject against an antigen which comprises administration of at least one peptide according to the invention; a dimer peptide comprising two peptides monomers, wherein each peptide monomer is according to the invention; a peptide combination comprising two or more peptide according to the invention; the nucleic acid or polynucleotide encoding a peptide according to the invention; the vector comprising the nucleic acid or polynucleotide encoding a peptide according to the invention; or the composition according to the invention.

In a further aspect the present invention relates to a method for reducing and/or delaying the pathological effects of a virus in a subject infected with said virus, the method comprising administering an effective amount of at least one peptide according to the invention; a dimer peptide comprising two peptides monomers, wherein each peptide monomer is according to the invention; a peptide combination comprising two or more peptide according to the invention; the nucleic acid or polynucleotide encoding a peptide according to the invention; the vector comprising the nucleic acid or polynucleotide encoding a peptide according to the invention; or the composition according to the invention.

In a further aspect the present invention relates to a peptide according to the invention for use as a medicament.

In a further aspect the present invention relates to a peptide according to the invention for treating the pathological effects of a virus in a subject infected with said virus.

DETAILED DISCLOSURE OF THE INVENTION Definitions

When terms such as “one”, “a” or “an” are used in this disclosure they mean “at least one”, or “one or more” unless otherwise indicated. Further, the term “comprising” is intended to mean “including” and thus allows for the presence of other constituents, features, conditions, or steps than those explicitly recited.

“HIV” generally denotes human immunodeficiency virus I.

“HIV disease” is composed of several stages including the acute HIV infection which often manifests itself as an influenza-like infection and the early and medium stage symptomatic disease, which has several non-characteristic symptoms such as skin rashes, fatigue, night sweats, slight weight loss, mouth ulcers, and fungal skin and nail infections. Most HIV infected will experience mild symptoms such as these before developing more serious illnesses. It is generally believed that it takes five to seven years for the first mild symptoms to appear. As HIV disease progresses, some individuals may become quite ill even if they have not yet been diagnosed with AIDS (see below), the late stage of HIV disease. Typical problems include chronic oral or vaginal thrush (a fungal rash or spots), recurrent herpes blisters on the mouth (cold sores) or genitals, ongoing fevers, persistent diarrhea, and significant weight loss. “AIDS” is the late stage HIV disease and is a condition which progressively reduces the effectiveness of the immune system and leaves individuals susceptible to opportunistic infections and tumors.

The term “cell-penetrating peptide” as used herein refers to any peptide with the capability to translocate across the plasma membrane into either cytoplasmic and/or nuclear compartments of eukaryotic and/or prokaryotic cells, such as into cytoplasm, nucleus, lysosome, endoplasmatic reticulum, golgi apparatus, mitocondria and/or chloroplast, seemingly energy-independently. This capability to translocate across the plasma membrane of a “cell-penetrating peptide” according to the invention may be non-invasive, energy-independent, non-saturable, and/or receptor independent. In one embodiment the term “cell-penetrating peptide” refers to a peptide, which is demonstrated to translocate across a plasma membrane as determined by the assay in example 1. It is to be understood that a cell-penetrating peptide according to the present invention may be translocated across the membrane with the sequence complete and intact, or alternatively partly degraded, but in a form where the antigens contained within this peptide is able to be presented within the cell to stimulate an immune response. Accordingly, a cell-penetrating peptide according to the present invention is a peptide that may be demonstrated to translocate across a plasma membrane as determined by the assay in example 1 and be demonstrated to stimulate an effective immune response.

The term “derived from an antigen” when in reference to a peptide derived from a source (such as a virus etc.) as used herein is intended to refer to a peptide which has been obtained (e.g., isolated, purified, etc.) from the source. Preferably, the peptide may be genetically engineered and/or chemically synthesized to be essentially identical to the native peptide of the source. The term includes the use of variants of known native peptide sequences, such as peptide sequences, where 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids of the native peptide sequence have been substituted with any other amino acid, such as conservative substitutions. Alternatively, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids have been removed or added to the native peptide sequence. Accordingly, in some embodiments, the peptides according to the present invention comprises the sequences X2 and/or X4, that is defined as a sequence of 8-30 amino acids, such as 8-20 amino acids derived from an antigen, wherein the peptide sequence of the antigen comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 substitutions, additions or deletions relative to the antigen, such as the addition of an arginine in the N- or C-terminal of the amino acid sequence of X2 and/or X4. The amino acids used in the amino acid sequences according to the invention may be in both L- and/or D-form. It is to be understood that both L- and D-forms may be used for different amino acids within the same peptide sequence. In some embodiments the amino acids within the peptide sequence are in L-form, such as natural amino acids. It is to be understood that any known antigen may be used in the constructs according to the present invention.

In some specific embodiments, the first 1, 2, or 3 amino acids in the N-terminal of the amino acid sequences according to the invention are in the D-form. It is assumed that the N-terminal trimming and thereby degradation of the peptides are somewhat delayed by having amino acids of the D-form in the N-terminal of these cell-penetrating peptides. Alternatively and in some embodiments, the first 1, 2, or 3 amino acids in the N-terminal of the amino acid sequences according to the invention are amino acids in beta or gamma forms. Beta amino acids have their amino group bonded to the beta carbon rather than the alpha carbon as in the 20 standard natural amino acids.

Alternatively the first 1, 2, or 3 amino acids in the N-terminal of the amino acid sequences according to the invention may be modified by incorporation of fluorine, or alternatively cyclic amino acids or other suitable non-natural amino acids are used.

A “variant” or “analogue” of a peptide refers to a peptide having an amino acid sequence that is substantially identical to a reference peptide, typically a native or “parent” polypeptide. The peptide variant may possess one or more amino acid substitutions, deletions, and/or insertions at certain positions within the native amino acid sequence.

“Conservative” amino acid substitutions are those in which an amino acid residue is replaced with an amino acid residue having a side chain with similar physicochemical properties. Families of amino acid residues having similar side chains are known in the art, and include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine, tryptophan), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). A particular form of conservative amino acid substitutions include those with amino acids, which are not among the normal 20 amino acids encoded by the genetic code. Since preferred embodiments of the present invention entail use of synthetic peptides, it is unproblematic to provide such “non-naturally occurring” amino acid residues in the peptides disclosed herein, and thereby it is possible to exchange the natural saturated carbon chains in the side chains of amino acid residues with shorter or longer saturated carbon chains—for instance, lysine may be substituted with an amino acid having an the side chain —(CH2)nNH3, where n is different from 4, and arginine may be substituted with an amino acid having the side chain —(CH2)nNHC(═NH2)NH2, where n is different from 3, etc. Similarly, the acidic amino acids aspartic acid and glutamic acid may be substituted with amino acid residues having the side chains —(CH2)nCOOH, where n>2.

The term “substantially identical” in the context of two amino acid sequences means that the sequences, when optimally aligned, such as by the programs GAP or BESTFIT using default gap weights, share at least about 50, at least about 60, at least about 70, at least about 80, at least about 90, at least about 95, at least about 98, or at least about 99 percent sequence identity. In one embodiment, residue positions that are not identical differ by conservative amino acid substitutions. Sequence identity is typically measured using sequence analysis software. Protein analysis software matches similar sequences using measures of similarity assigned to various substitutions, deletions and other modifications, including conservative amino acid substitutions. For instance, the publicly available GCG software contains programs such as “Gap” and “BestFit” which can be used with default parameters to determine sequence homology or sequence identity between closely related polypeptides, such as homologous polypeptides from different species of organisms or between a wild-type protein and a mutein thereof. See, e.g., GCG Version 6.1. Polypeptide sequences can also be compared using FASTA or ClustalW, applying default or recommended parameters. A program in GCG Version 6.1., FASTA (e.g., FASTA2 and FASTA3) provides alignments and percent sequence identity of the regions of the best overlap between the query and search sequences (Pearson, Methods Enzymol. 1990; 183:63-98; Pearson, Methods Mol. Biol. 2000; 132:185-219). Another preferred algorithm when comparing a sequence to a database containing a large number of sequences from various organisms, or when deducing the is the computer program BLAST, especially blastp, using default parameters. See, e.g., Altschul et al., J. Mol. Biol. 1990; 215:403-410; Altschul et al., Nucleic Acids Res. 1997; 25:3389-402 (1997); each herein incorporated by reference. “Corresponding” amino acid positions in two substantially identical amino acid sequences are those aligned by any of the protein analysis software mentioned herein, typically using default parameters.

An “isolated” molecule is a molecule that is the predominant species in the composition wherein it is found with respect to the class of molecules to which it belongs (i.e., it makes up at least about 50% of the type of molecule in the composition and typically will make up at least about 70%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or more of the species of molecule, e.g., peptide, in the composition). Commonly, a composition of a peptide molecule will exhibit 98%-99% homogeneity for peptide molecules in the context of all present peptide species in the composition or at least with respect to substantially active peptide species in the context of proposed use.

The term “linear sequence” as used herein refers to the specific sequence of amino acids connected by standard peptide bonds in standard N- to C-terminal direction. The peptide may contain only peptide bonds. However the term does not exclude that an amino acid within a sequence, such as within X3, may be connected, such as through the side chains, with another amino acid at a distant location within the peptide sequence, such as a distant location within X3.

In the context of the present invention, “treatment” or “treating” refers to preventing, alleviating, managing, curing or reducing one or more symptoms or clinically relevant manifestations of a disease or disorder, unless contradicted by context. For example, “treatment” of a patient in whom no symptoms or clinically relevant manifestations of a disease or disorder have been identified is preventive or prophylactic therapy, whereas “treatment” of a patient in whom symptoms or clinically relevant manifestations of a disease or disorder have been identified generally does not constitute preventive or prophylactic therapy.

The term “antigen” denotes a substance of matter which is recognized by the immune system's specifically recognizing components (antibodies, T-cells).

The term “immunogen” is in the present context intended to denote a substance of matter, which is capable of inducing an adaptive immune response in an individual, where said adaptive immune response targets the immunogen. In relation to the present invention, an immunogen will induce a humoral and/or cell-mediated immune response. In other words, an immunogen is an antigen, which is capable of inducing immunity.

The terms “epitope”, “antigenic determinant” and “antigenic site” are used interchangeably herein and denotes the region in an antigen or immunogen which is recognized by antibodies (in the case of antibody binding epitopes, also known as “B-cell epitopes”) or by T-cell receptors when the epitope is complexed to a Major histocompatibility complex (MHC) molecule (in the case of T-cell receptor binding epitopes, i.e. “T-cell epitopes”).

The term “immunogenically effective amount” has its usual meaning in the art, i.e. an amount of an immunogen, which is capable of inducing an immune response, which significantly engages pathogenic agents, which share immunological features with the immunogen.

The term “vaccine” is used for a composition comprising an immunogen and which is capable of inducing an immune response which is either capable of reducing the risk of developing a pathological condition or capable of inducing a therapeutically effective immune response which may aid in the cure of (or at least alleviate the symptoms of) a pathological condition.

The term “pharmaceutically acceptable” has its usual meaning in the art, i.e. it is used for a substance that can be accepted as part of a medicament for human use when treating the disease in question and thus the term effectively excludes the use of highly toxic substances that would worsen rather than improve the treated subject's condition.

A “T helper lymphocyte epitope” (a TH epitope) is peptide, which binds an MHC Class II molecule and can be presented on the surface of an antigen presenting cell (APC) bound to the MHC Class II molecule. An “immunological carrier” is generally a substance of matter which includes one or many TH epitopes, and which increase the immune response against an antigen to which it is coupled by ensuring that T-helper lymphocytes are activated and proliferate. Examples of known immunological carriers are the tetanus and diphtheria toxoids and keyhole limpet hemocyanin (KLH).

In the scaffold design according to the present invention, X2 and X4 defines a sequence of 8-30 amino acids, such as 8-20 amino acids derived from the antigen. This sequence of amino acids derived from an antigen may herein be referred to as an epitope.

Preferably the epitopes used in the scaffold according to the present invention are CTL epitopes. A “CTL inducing peptide” is a HLA Class I binding peptide that is capable of inducing a CTL response. In other embodiments the epitopes used in the scaffold design according to the present invention are HTL inducing peptides. A “HTL inducing peptide” is a HLA Class II binding peptide that is capable of inducing a HTL response.

The term “basic amino acid” as used herein refers to any amino acid including both natural and non-natural amino acids that has an isoelectric point above 6.3 (such as above 7.4) as measured according to Kice & Marvell “Modern Principles of organic Chemistry” (Macmillan, 1974) or Matthews and van Holde “Biochemistry” Cummings Publishing Company, 1996. Included within this definition are Arginine, Lysine, Homoarginine (Har), and Histidine as well as derivatives thereof. Suitable non-natural basic amino acids are e.g. as described in U.S. Pat. No. 6,858,396. Suitable positively charged amino acids includes non-natural alpha amino acids available from Bachem AG and includes alpha-amino-glycine, alpha,gamma-diaminobutyric acid, ornithine, alpha, beta-diaminoproprionic acid, alpha-difluoromethyl-ornithine, 4-amino-piperidine-4-carboxylic acid, 2,6-diamino-4-hexynoic acid, beta-(1-piperazinyl)-alanine, 4,5-dehydro-lysine, delta-hydroxy-lysine, omega-hydroxy-norarginine, homoarginine, omega-amino-arginine, omega-methyl-arginine, alpha-methyl-histidine, 2,5-diiodo-histidine, 1-methyl-histidine, 3-methyl-histidine, beta-(2-pyridyl)-alanine, beta-(3-pyridyl)-alanine, beta-(2-quinolyl)-alanine, 3-amino-tyrosine, 4-amino-phenylalanine, and spinacine. Furthermore, any mono or dicarboxylic amino acid is a suitable positively charged amino acid.

The term “neutral amino acid” as used herein refers to an amino acid that has an isoelectric point above between 4.8 and 6.3 as measured according to Kice & Marvell “Modern Principles of organic Chemistry” (Macmillan, 1974). The term “acidic amino acid” as used herein refers to an amino acid that has an isoelectric point below 4.8 as measured according to Kice & Marvell “Modern Principles of organic Chemistry” (Macmillan, 1974).

Unless otherwise indicated amino acids are abbreviated and mentioned by their standard nomenclature known to the person skilled in the art, such as with reference to “nomenclature and symbolism for amino acids and peptides” by the international union of pure and applied chemistry (IUPAC) (www.iupac.org).

Citrulline (In this document referred to with the one-letter symbol “B”) and/or homocitrulline are well known non-natural amino acids that in some embodiments may be used in the sequence defined by X1, X3, or X5.

In other alternative embodiments, tryptophan or tryptophan derivatives are used in the sequence defined by X1, X3, or X5. Any suitable tryptophan derivatives may be used. As used herein “tryptophan derivatives” means an unnatural modified tryptophan amino acid residue including those disclosed in U.S. Pat. No. 7,232,803, such as tri tert.-butyltryptophan, di-tert-butyl tryptophan, 7-benzyloxytryptophan, homotryptophan, 5′-aminoethyltryptophan (available as side chain Boc and N-alpha FMOC derivative from RSP Amino Acids Analogues Inc, Boston, Mass., USA), N-Acetylhomotryptophan (Toronto Research), 7-Benzyloxytryptophan (Toronto Research), Homotryptophan (Toronto Research), and tryptophan residues which have been substituted at the 1-, 2-, 5- and/or 7-position of the indole ring, positions 1- or 2- being preferred e.g. 5′ hydroxy tryptophan.

The term “antibody response” refers to the production of antibodies (e.g., IgM, IgA, IgG) which bind to an antigen of interest, this response is measured for instance by assaying sera by antigen ELISA.

The term “adjuvant” as used herein refers to any compound which, when delivered together or simultaneously with an antigen, non-specifically enhances the immune response to that antigen. Exemplary adjuvants include but are not limited to oil in water and water in oil adjuvants, aluminum-based adjuvants (e.g., AIOH, AIPO4, etc), and Montanide ISA 720.

The terms “patient” and “subject” refer to a mammal that may be treated using the methods of the present invention.

As used herein, the term “immune response” refers to the reactivity of an organism's immune system in response to an antigen. In vertebrates, this may involve antibody production, induction of cell-mediated immunity, and/or complement activation (e.g., phenomena associated with the vertebrate immune system's prevention and resolution of infection by microorganisms). In preferred embodiments, the term immune response encompasses but is not limited to one or more of a “lymphocyte proliferative response,” a “cytokine response,” and an “antibody response.”

The term “net charge” as used herein with reference to a peptide sequence refers to the total electric charge of the peptide sequence represented by the sum of charges of each individual amino acid in the peptide sequence, wherein each basic amino acid are given a charge of +1, each acidic amino acid a charge of −1, and each neutral amino acid a charge of 0. Accordingly, the net charge will depend on the number and identities of charged amino acids.

TABLE 1  Specific peptides according to the invention Placement with reference to positions in SEQ ID NO: 3; SEQ ID NO: 6; SEQ ID NO: 7, Modified (m) SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: Reference ID 46, and SEQ x2 x3 x4 ID NO: 126. P-biotin x1 QIKIWFQN RR MKWKK Modified X2- x4- antigen N-Biotin R PVVHLTL R QAGDDFSR x5 (m) seq seq HCV SP_2 RR GYIPLVGAPLG BGR VARALAHGVRV 135-145 147-157 HCV SP_3 R GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP_4 R GYIPLVGAPLG RRR VARALAHGVRV R 135-145 147-157 HCV SP_5 RR GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP_6 RR GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP_7 BR GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP_8 RRR GYIPLVGAPLG BR VARALAHGVRV 135-145 147-157 HCV SP_9 R GYIPLVGAPLG KKK VARALAHGVRV 135-145 147-157 HCV SP_10 R GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP_11 KK GYIPLVGAPLG KK VARALAHGVRV 135-145 147-157 HCV SP_12 W GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP_13 WW GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP_14 EE GYIPLVGAPLG EE VARALAHGVRV 135-145 147-157 HCV SP_15 GG GYIPLVGAPLG GG VARALAHGVRV 135-145 147-157 HCV SP_16 EE GYIPLVGAPLG RR VARALAHGVRV 135-145 147-57 HCV SP_17 RR GYIPLVGAPLG LRR VARALAHGVRV 135-145 147-157 HCV SP21: WW GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP22: WW GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP23: WW GYIPLVGAPLG R VARALAHGVRV 135-145 147-157 HCV SP24: R GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV 51_BIotin RR GYLPAVGAPIG BR VIRVIAHGLRL m 135-144 147-157 HCV 51b_BIotin RR GYIPLVGAPLG BR VARALAHGVRV 135-145 147-157 HCV 51_n GYIPLVGAPLG G VARALAHGVRV 135-145 147-157 HCV SP51_1: WW GYLPAVGAPI RR VIRVIAHGLRL m 135-144 147-157 HCV SP1_C* GYIPLVGAPLG G VARALAHGVRV 135-145 147-157 HCV SP2_c RR GYIPLVGAPLG BGR VARALAHGVRV 135-145 147-157 HCV SP3_c R GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP4_c R GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP5_c RR GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP6_c RR GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP7_c BR GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP8_c RRR GYIPLVGAPLG BR VARALAHGVRV 135-145 147-157 HCV SP9_c R GYIPLVGAPLG KKK VARALAHGVRV 135-145 147-157 HCV SP10_c R GYIPLVGAPLG RRR VARALAHGVRV 135-145 147-157 HCV SP11_c  KK GYIPLVGAPLG KK VARALAHGVRV 135-145 147-157 HCV SP12_c W GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP13_c WW GYIPLVGAPLG RR VARALAHGVRV 135-145 147-157 HCV SP17_c RR GYIPLVGAPLG LRR VARALAHGVRV 135-145 147-157 HCV SP61_2_ RR NYVTGNIPG BR GITFSIFLIVS 163-171 171-181 HCV SP61b_2_ WW NYATGNLPG RR CSFSIFLLAL m 163-171 171-181 HCV SP61_3_ WW NYVTGNIPG BR GITFSIFLIVS 163-171 171-181 HCV SP61_4_ WW NYVTGNIPG RR GITFSIFLIVS 163-171 171-181 HCV 61b_BIotin RR NYATGNLPG RR GCSFSIFLLAL 163-171 171-181 HCV SP25 RR VTGNIPGSTYSG BR GITFSIYLIVS m 165-175 171-181 HCV 42_BIotin RR IRNLGRVIETLTG BR LZGYIPLIGA m 116-128 133-142 HCV 42b_BIotin RR SRNLGKVIDTLTC BR LMGYIPLVGA 116-128 133-142 HCV 42n-BIOTIN SRNLGKVIDTLTC GFAD LMGYIPLVGA 116-129 133-142 HCV SP42_1_ WW IRNLGRVIETLT RR LZGYIPLIGA m 116-128 133-142 HCV SP42b_1_ WW SRNLGKVIDTLTC RR LMGYIPLVGA 116-129 133-142 HCV BI310-11_ RR GGGQIIGGNYLIP PBIGVRATB 26-38 42-50 Biotin HCV BI310-11n_ GGGQIVGGVYLLP GPRLGVRATR 26-38 42-50 Biotin HCV BI310-11n_ RR GGGQIVGGVYLLP GPRLGVRATR 26-38 42-50 sc_Biotin HCV SP11b-1- WW GGGQIVGGVYLLP RR GPRLGVRAT 26-38 42-50 FLU BI100-12 BR LIFLARSALIV RGSVAHKS 256-266 267-274 FLU BI100-22b ED LIFLARSALIL RGSVAHKS 255-266 267-274 FLU 120b_BIotin BR LIFLARSALIL BGR SALILRGSVAHK 255-266 267-274 FLU BI100-18b SAYERMCNIL KGK FQTAAQRAMM 217-226 230-239 FLU BI100-19 SAYERZVNIL KGK FQTAAQRAVZ 217-226 230-239 FLU 190_BIotin BR TAYERZCNIL BRGR FQTVVQBA 217-226 230-237 FLU 190b_BIotin BR IAYERMCNIL LBRGK FQTAAQRA 217-226 230-237 FLU 190n-BIOTIN IAYERMCNIL KGK FQTAAQRA 217-226 230-237 FLU BI100-24b LFFKCIYRLFKHG KR GPSTEGVPESM 46-59 62-72 L FLU BI100-26 BRR LFFKTITRLFBHG RR LLSTEGVPNSZ 46-59 62-72 L FLU 260_Biotin BR GLEPLVIAGILA RR GSLVGLLHIVL 23-33 30-40 FLU 260b_Biotin BR GSDPLVVAASIV RR ASIVGILHLIL 23-33 30-40 CMV BI 050-sc1 R NLVPMVATV RR NLVPMVATV B 485-493 485-493 CMV BI 050-sc2 R NLVPMVATV BRR NLVPMVATV B 485-493 485-493 CMV BI 050-sc5 R NIVPZVVTA RR NIVPZVVTA B m 485-493 485-493 HIV N10 PEVIPMFSALS EGA TPQDLNTMLN HIV V10 R FIIPXFTALSG GRR ALLYGATPYAIG HIV N13 K ALGPAATL EE MMTACQGVG Neg SP_18 RR GPVVHLTL RR GQAGDDFS c mod Neg SP_19 RR GPVVHLTL RR GQAGDDFS c mod Neg SP_20 RR GPVVHLTL RGR GQAGDDFS c mod HPV RR LECVYCKQQLL RR EVYDFAFRDLC 35-45 48-58 HPV RR GVYDFAFRDLC RR GFAFRDLCIVY R 49-58 52-61 HPV RR GVFDYAFRDIN RR GFAYRDINLAY R 49-58 52-61 CMV RR GATPVDLLGA RR GALNLCLPM R 498-506 505-514 CMV RR GVTPAGLIGV RR GALQIBLPL R 498-506 505-514 HPV RR VDIRTLEDLL RR GTLGIVCPIG R 74-83 84-93

As used herein the one-letter-code ‘Z’ refers to the non-natural amino acid norleucine.

TABLE 2  Specific peptides according to the invention Antigen X1 X2 X3 X4 X5 HCV R GYIPLVGAPLG RRR VARALAHGVRV R HCV R GYLPAVGAPIG RRR VIRVIAHGLRL R HCV RR GYIPLVGAPLG RR VARALAHGVRV HCV RR GYIPLVGAPLG RRR VARALAHGVRV HCV RR SRNLGKVIDTLTC RR LMGYIPLVGA HCV RR GGGQIVGGVYLLP RR GPRLGVRATR HCV W GYIPLVGAPLG RR VARALAHGVRV HCV RR IRNLGRVIETLTL RR IRNLGRVIETL R ZGYIPLIGA TLZGYIPLIGA Flu BR TAYERZCNIL BRGR FQTVVQBA cmv R NLVPMVATV BRR NLVPMVATV B As used herein the one-letter-code ‘Z’ refers to the non-natural amino acid norleucine.

Antigens

Examples of viral antigens for use with the present invention include, but are not limited to, e.g., HIV, HCV, CMV, HPV, Influenza, adenoviruses, retroviruses, picornaviruses, etc. Non-limiting example of retroviral antigens such as retroviral antigens from the human immunodeficiency virus (HIV) antigens such as gene products of the gag, pol, and env genes, the Nef protein, reverse transcriptase, and other HIV components; hepatitis viral antigens such as the S, M, and L proteins of hepatitis B virus, the pre-S antigen of hepatitis B virus, and other hepatitis, e.g., hepatitis A, B, and C, viral components such as hepatitis C viral RNA; influenza viral antigens such as hemagglutinin and neuraminidase and other influenza viral components; measles viral antigens such as the measles virus fusion protein and other measles virus components; rubella viral antigens such as proteins E1 and E2 and other rubella virus components; rotaviral antigens such as VP7sc and other rotaviral components; cytomegaloviral antigens such as envelope glycoprotein B and other cytomegaloviral antigen components; respiratory syncytial viral antigens such as the RSV fusion protein, the M2 protein and other respiratory syncytial viral antigen components; herpes simplex viral antigens such as immediate early proteins, glycoprotein D, and other herpes simplex viral antigen components; varicella zoster viral antigens such as gpl, gpll, and other varicella zoster viral antigen components; Japanese encephalitis viral antigens such as proteins E, M-E, M-E-NSI, NSI, NS1-NS2A, 80% E, and other Japanese encephalitis viral antigen components; rabies viral antigens such as rabies glycoprotein, rabies nucleoprotein and other rabies viral antigen components. See Fundamental Virology, Second Edition, eds. Fields, B. N. and Knipe, D. M. (Raven Press, New York, 1991) for additional examples of viral antigens.

The epitopes to be incorporated into the scaffold design according to the present invention may be derived from an adenovirus, retrovirus, picornavirus, herpesvirus, rotavirus, hantavirus, coronavirus, togavirus, flavirvirus, rhabdovirus, paramyxovirus, orthomyxovirus, bunyavirus, arenavirus, reovirus, papilomavirus, parvovirus, poxvirus, hepadnavirus, or spongiform virus. In certain specific, non-limiting examples, the viral antigen are peptides obtained from at least one of HIV, CMV, hepatitis A, B, and C, influenza, measles, polio, smallpox, rubella; respiratory syncytial, herpes simplex, varicella zoster, Epstein-Barr, Japanese encephalitis, rabies, Influenza, and/or cold viruses.

HCV:

Peptides according to the present invention may comprise a known antigen. For antigens derived from HCV these antigens may be derived from the Core, E1, E2, P7, NS2, NS3, NS4 (NS4A and NS4B) and NS5 (NS5A and NS5B) protein of the Hepatitis C Virus (HCV). The epitopes are those which elicit a HLA class I and/or class II restricted T lymphocyte response in an immunized host. More specific, the HLA class I restricted peptides of the present invention may bind to at least one HLA molecule of the following HLA class I groups: HLA-A*01, HLA-A*02, HLA-A*03, HLA-A*11, HLA-A*24, HLA-B*07, HLA-B*08, HLA-B*35, HLA-B*40, HLA-B*44, HLA-Cw3, HLA-Cw4, HLA-Cw6 or HLA-Cw7. The HLA class II restricted peptides of the present invention may bind to at least one HLA molecule of the following HLA class II groups: HLA-DRB1, -DRB2, -DRB3, -DRB4, -DRB5, -DRB6, -DRB7, -DRB8 or -DRB9.

MHC binding HCV peptides that may be used according to the present invention as epitopes are disclosed in e.g. WO02/34770 (Imperial College Innovations Ltd), WO01/21189 and WO02/20035 (Epimmune), WO04/024182 (Intercell), WO95/25122 (The Scripps Research Institute), WO95/27733 (Government of the USA, Department of Health and Human Services), EP 0935662 (Chiron), WO02/26785 (Immusystems GmbH), WO95/12677 (Innogenetics N.V), WO97/34621 (Cytel Corp), and EP 1652858 (Innogenetics N.V.).

In other embodiments, the scaffold design according to the present invention comprises a PADRE peptide, such as the universal T cell epitope called PADRE as disclosed in WO95/07707 (Epimmune) the content of which are enclosed herein by reference. A ‘PanDR binding peptide or PADRE peptide” is a member of a family of molecules that binds more that one HLA class II DR molecule. PADRE binds to most HLA-DR molecules and stimulates in vitro and in vivo human helper T lymphocyte (HTL) responses. Alternatively T-help epitopes can be used from universally used vaccines such as tetanos toxoid.

In a further embodiment, the peptides in the composition or polyepitopic peptide are characterized in that they are derived from a HCV protein, or more specifically from at least one of the following HCV regions selected from the group consisting of Core, E1, E2/NS1, NS2, NS3, NS4A, NS4B, NS5A and NS5B. Even more preferred is that peptides are characterized in that they are present in the HCV consensus sequence of genotype 1a, 1b and/or 3 a.

Other HLA class I and II binding peptides that may be used according to the invention may be identified by the method as described in WO03/105058—Algonomics, by the method as described by Epimmune in WO01/21189 and/or by three public database prediction servers, respectively Syfpeithi, BIMAS and nHLAPred. It is also an aspect of this present invention that each peptide may be used within the scaffold design of the invention in combination with the same peptide as multiple repeats, or with any other peptide(s) or epitope(s).

CMV:

The epitopes to be incorporated into the scaffold design according to the present invention may be derived from cytomegalovirus (CMV) including CMV glycoproteins gB and gH.

Influenza:

The epitopes to be incorporated into the scaffold design according to the present invention may be derived from fragments or portions of Influenza hemagglutinin (HA) or Influenza neuraminidase (NA), nucleoprotein (NP), M1, M2, NS1, NEP, PA, PB1, PB1-F2, PB2 for each of the subgroups, such as H1N1, H2N2 og H3N2.

Suitable epitopes may be derived from an HA protein of one, or more than one subtype, including H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15 or H16 or fragment or portion thereof. Examples of subtypes comprising such HA proteins include A/New Caledonia/20/99 (H1N1) A/Indonesia/5/2006 (H5N1), A/chicken/New York/1995, A/herring gull/DE/677/88 (H2N8), A/Texas/32/2003, A/mallard/MN/33/00, A/duck/Shanghai/1/2000, A/northern pintail/TX/828189/02, A/Turkey/Ontario/6118/68 (H8N4), A/shoveler/Iran/G54/03, A/chicken/Germany/N/1949 (H10N7), A/duck/England/56 (H11N6), A/duck/Alberta/60/76 (H12N5), A/Gull/Maryland/704/77 (H13N6), A/Mallard/Gurjev/263/82, A/duck/Australia/341/83 (H15N8), A/black-headed gull/Sweden/5/99 (H16N3), B/Lee/40, C/Johannesburg/66, A/PuertoRico/8/34 (H1N1), A/Brisbane/59/2007 (H1N1), A/Solomon Islands 3/2006 (H1N1), A/Brisbane 10/2007 (H3N2), A/Wisconsin/67/2005 (H3N2), B/Malaysia/2506/2004, B/Florida/4/2006, A/Singapore/1/57 (H2N2), A/Anhui/1/2005 (H5N1), A/Vietnam/1194/2004 (H5N1), A/Teal/HongKong/W312/97 (H6N1), A/Equine/Prague/56 (H7N7), A/HongKong/1073/99 (H9N2)).

In some embodiments of the invention, the HA protein may be an H1, H2, H3, H5, H6, H7 or H9 subtype. In other embodiments, the H1 protein may be from the A/New Caledonia/20/99 (H1N1), A/PuertoRico/8/34 (H1N1), A/Brisbane/59/2007 (H1N1), or A/Solomon Islands 3/2006 (H1N1) strain. The H3 protein may also be from the A/Brisbane 10/2007 (H3N2) or A/Wisconsin/67/2005 (H3N2) strain. In other embodiments, the H2 protein may be from the A/Singapore/1/57 (H2N2) strain. The H5 protein may be from the A/Anhui/1/2005 (H5N1), A/Vietnam/1194/2004 (H5N1), or A/Indonesia/5/2005 strain. In other embodiments, the H6 protein may be from the A/Teal/HongKong/W312/97 (H6N1) strain. The H7 protein may be from the A/Equine/Prague/56 (H7N7) strain. In other embodiments, the H9 protein is from the A/HongKong/1073/99 (H9N2) strain. In other embodiments, the HA protein may be from an influenza virus may be a type B virus, including B/Malaysia/2506/2004 or B/Florida/4/2006. The influenza virus HA protein may be H5 Indonesia.

Human Immunodeficiency Virus (HIV):

For HIV, the epitopes to be incorporated into the scaffold design according to the present invention may be derived from the group consisting of gp120, gp160, gp41, p24gag or p55gag derived from HIV, including members of the various genetic subtypes.

Human Papillomavirus (HPV):

For HPV, the epitopes to be incorporated into the scaffold design according to the present invention may be derived from the group consisting E1, E2, E3, E4, E6 and E7, L1 and L2 proteins. The epitopes may be derived from any type including types 8, 11, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, and 59.

Carriers, Adjuvants and Vehicles—Delivery

The isolated cell-penetrating peptides according to the invention may be delivered by various means and within various compositions, herein referred to as “compositions”, “vaccine compositions” or “pharmaceutical compositions”. The peptides of the present invention and pharmaceutical and vaccine compositions of the invention are useful for administration to mammals, particularly humans, to treat and/or prevent virus infection. Vaccine compositions containing the peptides of the invention are administered to a patient infected with the virus in question or to an individual susceptible to, or otherwise at risk for, virus infection to elicit an immune response against the specific antigens and thus enhance the patient's own immune response capabilities.

Various art-recognized delivery systems may be used to deliver the peptides, into appropriate cells. The peptides can be delivered in a pharmaceutically acceptable carrier or as colloidal suspensions, or as powders, with or without diluents. They can be “naked” or associated with delivery vehicles and delivered using delivery systems known in the art.

A “pharmaceutically acceptable carrier” or “pharmaceutically acceptable adjuvant” is any suitable excipient, diluent, carrier and/or adjuvant which, by themselves, do not induce the production of antibodies harmful to the individual receiving the composition nor do they elicit protection. Preferably, a pharmaceutically acceptable carrier or adjuvant enhances the immune response elicited by an antigen. Suitable carriers or adjuvant typically comprise one or more of the compounds included in the following non-exhaustive list: large slowly metabolized macromolecules such as proteins, polysaccharides, polylactic acids, polyglycolic acids, polymeric amino acids, amino acid copolymers and inactive virus particles; aluminium hydroxide, aluminium phosphate (see International Patent Application Publication No. WO93/24148), alum (KAI(SO4)2.12H2O), or one of these in combination with 3-O-deacylated monophosphoryl lipid A (see International Patent Application Publication No. WO93/19780);

N-acetyl-muramyl-L-threonyl-D-isoglutamine (see U.S. Pat. No. 4,606,918), N-acetyl-normuramyl-L-alanyl-D-isoglutamine, N-acetylmuramyl-L-alanyl-D-isoglutamyl-L-alanine2-(1′,2′-dipalmitoyl-sn-glycero-3-hydroxyphosphoryloxy) ethylamine; RIBI (ImmunoChem Research Inc., Hamilton, Mont., USA) which contains monophosphoryl lipid A (i.e., a detoxified endotoxin), trehalose-6,6-dimycolate, and cell wall skeleton (MPL+TDM+CWS) in a 2% squalene/Tween 80 emulsion. Any of the three components MPL, TDM or CWS may also be used alone or combined 2 by 2; adjuvants such as Stimulon (Cambridge Bioscience, Worcester, Mass., USA), SAF-1 (Syntex); adjuvants such as combinations between QS21 and 3-de-O-acetylated monophosphoryl lipid A (see International Application No. WO94/00153) which may be further supplemented with an oil-in-water emulsion (see, e.g., International Application Nos. WO95/17210, WO97/01640 and WO9856414) in which the oil-in-water emulsion comprises a metabolisable oil and a saponin, or a metabolisable oil, a saponin, and a sterol, or which may be further supplemented with a cytokine (see International Application No. WO98/57659); adjuvants such as MF-59 (Chiron), or poly[di(carboxylatophenoxy) phosphazene] based adjuvants (Virus Research Institute); blockcopolymer based adjuvants such as Optivax (Vaxcel, Cytrx) or inulin-based adjuvants, such as Algammulin and Gammalnulin (Anutech); Complete or Incomplete Freund's Adjuvant (CFA or IFA, respectively) or Gerbu preparations (Gerbu Biotechnik); a saponin such as QuilA, a purified saponin such as QS21, QS7 or QS17, -escin or digitonin; immunostimulatory oligonucleotides comprising unmethylated CpG dinucleotides such as [purine-purine-CG-pyrimidine-pyrimidine] oligonucleotides. These immunostimulatory oligonucleotides include CpG class A, B, and C molecules (Coley Pharmaceuticals), ISS (Dynavax), Immunomers (Hybridon). Immunostimulatory oligonucleotides may also be combined with cationic peptides as described, e.g., by Riedl et al. (2002); Immune Stimulating Complexes comprising saponins, for example Quil A (ISCOMS); excipients and diluents, which are inherently non-toxic and non-therapeutic, such as water, saline, glycerol, ethanol, isopropyl alcohol, DMSO, wetting or emulsifying agents, pH buffering substances, preservatives, and the like; a biodegradable and/or biocompatible oil such as squalane, squalene, eicosane, tetratetracontane, glycerol, peanut oil, vegetable oil, in a concentration of, e.g., 1 to 10% or 2.5 to 5%; vitamins such as vitamin C (ascorbic acid or its salts or esters), vitamin E (tocopherol), or vitamin A; carotenoids, or natural or synthetic flavanoids; trace elements, such as selenium; any Toll-like receptor ligand as reviewed in Barton and Medzhitov (2002).

Any of the afore-mentioned adjuvants comprising 3-de-O-acetylated monophosphoryl lipid A, said 3-de-O-acetylated monophosphoryl lipid A may be forming a small particle (see International Application No. WO94/21292).

In any of the aforementioned adjuvants MPL or 3-de-O-acetylated monophosphoryl lipid A can be replaced by a synthetic analogue referred to as RC-529 or by any other amino-alkyl glucosaminide 4-phosphate (Johnson et al. 1999, Persing et al. 2002). Alternatively it can be replaced by other lipid A analogues such as OM-197 (Byl et al. 2003).

A “pharmaceutically acceptable vehicle” includes vehicles such as water, saline, physiological salt solutions, glycerol, ethanol, etc. Auxiliary substances such as wetting or emulsifying agents, pH buffering substances, preservatives may be included in such vehicles. Delivery systems known in the art are e.g. lipopeptides, peptide compositions encapsulated in poly-DL-lactide-co-glycolide (“PLG”), microspheres, peptide compositions contained in immune stimulating complexes (ISCOMS), multiple antigen peptide systems (MAPs), viral delivery vectors, particles of viral or synthetic origin, adjuvants, liposomes, lipids, microparticles or microcapsules, gold particles, nanoparticles, polymers, condensing agents, polysaccharides, polyamino acids, dendrimers, saponins, QS21, adsorption enhancing materials, fatty acids or, naked or particle absorbed cDNA.

Typically, a vaccine or vaccine composition is prepared as an injectable, either as a liquid solution or suspension. Injection may be subcutaneous, intramuscular, intravenous, intraperitoneal, intrathecal, intradermal, or intraepidermal. Other types of administration comprise electroporation, implantation, suppositories, oral ingestion, enteric application, inhalation, aerosolization or nasal spray or drops. Solid forms, suitable for dissolving in, or suspension in, liquid vehicles prior to injection may also be prepared. The preparation may also be emulsified or encapsulated in liposomes for enhancing adjuvant effect.

A liquid formulation may include oils, polymers, vitamins, carbohydrates, amino acids, salts, buffers, albumin, surfactants, or bulking agents. Preferably carbohydrates include sugar or sugar alcohols such as mono-, di-, tri-, oligo- or polysaccharides, or water-soluble glucans.

The saccharides or glucans can include fructose, dextrose, lactose, glucose, mannose, sorbose, xylose, maltose, sucrose, dextran, pullulan, dextrin, alpha and beta cyclodextrin, soluble starch, hydroxethyl starch and carboxymethylcellulose, or mixtures thereof. Sucrose is most preferred. “Sugar alcohol” is defined as a C4 to C8 hydrocarbon having an —OH group and includes galactitol, inositol, mannitol, xylitol, sorbitol, glycerol, and arabitol. Mannitol is most preferred. These sugars or sugar alcohols mentioned above may be used individually or in combination. There is no fixed limit to the amount used as long as the sugar or sugar alcohol is soluble in the aqueous preparation. Preferably, the sugar or sugar alcohol concentration is between 1.0% (w/v) and 7.0% (w/v), more preferable between 2.0 and 6.0% (w/v). Preferably amino acids include levorotary (L) forms of carnitine, arginine, and betaine; however, other amino acids may be added. Preferred polymers include polyvinylpyrrolidone (PVP) with an average molecular weight between 2,000 and 3,000, or polyethylene glycol (PEG) with an average molecular weight between 3,000 and 5,000. It is also preferred to use a buffer in the composition to minimize pH changes in the solution before lyophilization or after reconstitution. Any physiological buffer may be used, but citrate, phosphate, succinate, and glutamate buffers or mixtures thereof are preferred. Most preferred is a citrate buffer. Preferably, the concentration is from 0.01 to 0.3 molar. Surfactants that can be added to the formulation are shown in EP patent applications No. EP 0 270 799 and EP 0 268 110.

Additionally, polypeptides can be chemically modified by covalent conjugation to a polymer to increase their circulating half-life, for example. Preferred polymers, and methods to attach them to peptides, are shown in U.S. Pat. Nos. 4,766,106; 4,179,337; 4,495,285; and 4,609,546. Preferred polymers are polyoxyethylated polyols and polyethylene glycol (PEG). PEG is soluble in water at room temperature and has the general formula:

R(O—CH2-CH2)nO-R where R can be hydrogen, or a protective group such as an alkyl or alkanol group. Preferably, the protective group has between 1 and 8 carbons, more preferably it is methyl. The symbol n is a positive integer, preferably between 1 and 1.000, more preferably between 2 and 500. The PEG has a preferred average molecular weight between 1000 and 40.000, more preferably between 2000 and 20.000, most preferably between 3.000 and 12.000. Preferably, PEG has at least one hydroxy group, more preferably it is a terminal hydroxy group. It is this hydroxy group which is preferably activated. However, it will be understood that the type and amount of the reactive groups may be varied to achieve a covalently conjugated PEG/polypeptide of the present invention.

Water soluble polyoxyethylated polyols are also useful in the present invention. They include polyoxyethylated sorbitol, polyoxyethylated glucose, polyoxyethylated glycerol (POG), etc. POG is preferred. One reason is because the glycerol backbone of polyoxyethylated glycerol is the same backbone occurring naturally in, for example, animals and humans in mono-, di-, triglycerides. Therefore, this branching would not necessarily be seen as a foreign agent in the body. The POG has a preferred molecular weight in the same range as PEG. The structure for POG is shown in Knauf et al., 1988, and a discussion of POG/IL-2 conjugates is found in U.S. Pat. No. 4,766,106.

Another drug delivery system for increasing circulatory half-life is the liposome. The peptides and nucleic acids of the invention may also be administered via liposomes, which serve to target a particular tissue, such as lymphoid tissue, or to target selectively infected cells, as well as to increase the half-life of the peptide and nucleic acids composition. Liposomes include emulsions, foams, micelles, insoluble monolayers, liquid crystals, phospholipid dispersions, lamellar layers and the like. In these preparations, the peptide or nucleic acids to be delivered is incorporated as part of a liposome or embedded, alone or in conjunction with a molecule which binds to a receptor prevalent among lymphoid cells, such as monoclonal antibodies which bind to the CD45 antigen, or with other therapeutic or immunogenic compositions. Thus, liposomes either filled or decorated with a desired peptide or nucleic acids of the invention can be directed to the site of lymphoid cells, where the liposomes then deliver the peptide and nucleic acids compositions. Liposomes for use in accordance with the invention are formed from standard vesicle-forming lipids, which generally include neutral and negatively charged phospholipids and a sterol, such as cholesterol. The selection of lipids is generally guided by consideration of, e.g., liposome size, acid lability and stability of the liposomes in the blood stream. A variety of methods are available for preparing liposomes, as described in, e.g., Szoka et al, 1980, and U.S. Pat. Nos. 4,235,871, 4,501,728, 4,837,028, and 5,019,369.

For targeting cells of the immune system, a ligand to be incorporated into the liposome can include, e.g., antibodies or fragments thereof specific for cell surface determinants of the desired immune system cells. A liposome suspension containing a peptide may be administered intravenously, locally, topically, etc. in a dose which varies according to, inter alia, the manner of administration, the peptide being delivered, and the stage of the disease being treated. For example, liposomes carrying either immunogenic polypeptides are known to elicit CTL responses in vivo (Reddy et al., 1992; Collins et al., 1992; Fries et al., 1992; Nabel et al., 1992).

After the liquid pharmaceutical composition is prepared, it is preferably lyophilized to prevent degradation and to preserve sterility. Methods for lyophilizing liquid compositions are known to those of ordinary skill in the art. Just prior to use, the composition may be reconstituted with a sterile diluent (Ringer's solution, distilled water, or sterile saline, for example) which may include additional ingredients. Upon reconstitution, the composition is preferably administered to subjects using those methods that are known to those skilled in the art.

Use of the Peptides for Evaluating Immune Responses.

The peptides according to the present invention may be used as diagnostic reagents. For example, a peptide of the invention may be used to determine the susceptibility of a particular individual to a treatment regimen which employs the peptide or related peptides, and thus may be helpful in modifying an existing treatment protocol or in determining a prognosis for an affected individual. In addition, the peptides may also be used to predict which individuals will be at substantial risk for developing a chronic virus infection.

Accordingly, the present invention relates to a method of determining the outcome for a subject exposed to a virus, comprising the steps of determining whether the subject has an immune response to one or more peptides according to the present invention.

In a preferred embodiment of the invention, the peptides as described herein can be used as reagents to evaluate an immune response. The immune response to be evaluated can be induced by using as an immunogen any agent that may result in the production of antigen-specific CTLs or HTLs that recognize and bind to the peptide(s) to be employed as the reagent. The peptide reagent need not be used as the immunogen. Assay systems that can be used for such an analysis include relatively recent technical developments such as tetramers, staining for intracellular lymphokines and interferon release assays, or ELISPOT assays.

For example, a peptide of the invention may be used in a tetramer staining assay to assess peripheral blood mononuclear cells for the presence of antigen-specific CTLs following exposure to an antigen or an immunogen. The HLA-tetrameric complex is used to directly visualize antigen-specific CTLS (see, e.g., Ogg et al., 1998; and Altman et al., 1996) and determine the frequency of the antigen-specific CTL population in a sample of peripheral blood mononuclear cells. A tetramer reagent using a peptide of the invention may be generated as follows: a peptide that binds to an HLA molecule is refolded in the presence of the corresponding HLA heavy chain and beta2-microglobulin to generate a trimolecular complex. The complex is biotinylated at the carboxyl terminal end of the heavy chain at a site that was previously engineered into the protein. Tetramer formation is then induced by the addition of streptavidin. By means of fluorescently labeled streptavidin, the tetramer can be used to stain antigen-specific cells. The cells may then be identified, for example, by flow cytometry. Such an analysis may be used for diagnostic or prognostic purposes. Cells identified by the procedure can also be used for therapeutic purposes. As an alternative to tetramers also pentamers or dimers can be used (Current Protocols in Immunology (2000) unit 17.2 supplement 35)

Peptides of the invention may also be used as reagents to evaluate immune recall responses. (see, e.g., Bertoni et al., 1997 and Perma et al., 1991.). For example, patient PBMC samples from individuals with HCV infection may be analyzed for the presence of antigen-specific CTLs or HTLs using specific peptides. A blood sample containing mononuclear cells may be evaluated by cultivating the PBMCs and stimulating the cells with a peptide of the invention. After an appropriate cultivation period, the expanded cell population may be analyzed, for example, for cytotoxic activity (CTL) or for HTL activity.

The peptides may also be used as reagents to evaluate the efficacy of a vaccine.

PBMCs obtained from a patient vaccinated with an immunogen may be analyzed using, for example, either of the methods described above. The patient is HLA typed, and peptide epitope reagents that recognize the allele-specific molecules present in that patient are selected for the analysis. The immunogenicity of the vaccine is indicated by the presence of epitope-specific CTLs and/or HTLs in the PBMC sample.

The peptides of the invention may also be used to make antibodies, using techniques well known in the art (see, e.g. CURRENT PROTOCOLS IN IMMUNOLOGY, Wiley/Greene, NY; and Antibodies A Laboratory Manual, Harlow and Lane, Cold Spring Harbor Laboratory Press, 1989). Such antibodies include those that recognize a peptide in the context of an HLA molecule, i.e., antibodies that bind to a peptide-MHC complex.

SPECIFIC EMBODIMENTS OF THE INVENTION

The present invention concerns a peptide an isolated cell-penetrating peptide comprising the following structure


X1-X2-X3-X4-X5  (formula I),

wherein X1 and X3 independently defines a linear sequence of any 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof; X2 defines a linear sequence of 8-30 amino acids derived from an antigen; X4 defines a linear sequence of 8-30 amino acids derived from said antigen, said sequence X4 being different from X2; and wherein X5 is any one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some specific embodiments the sequence of X4 is identical to the sequence of X2.

In some embodiments the isolated cell-penetrating peptide has a total of not more than 60 amino acids.

In some embodiments X1 defines a linear sequence of any 1, 2, 3, or 4 amino acids independently selected from any basic amino acid, tryptophan, or a derivative thereof.

In some embodiments X1 defines a linear sequence in any order of one citrulline and any 1, 2, or 3 amino acids independently selected from any basic amino acid, tryptophan, or a derivative thereof.

In some embodiments X3 defines a linear sequence of any 1, 2, 3, or 4 amino acids independently selected from any basic amino acid.

In some embodiments X1 defines a linear sequence of any 1, 2, 3, or 4 amino acids independently selected from any basic amino acid.

In some embodiments X3 defines a linear sequence in any order of one citrulline and of any 1, 2, or 3 amino acids independently selected from any basic amino acid.

In some embodiments the sequence of amino acids defined by X2-X3-X4 of formula I as defined in claim 1 is not found in the native sequence of said antigen.

In some embodiments the sequence of amino acids defined by X1-X2-X3-X4 of formula I as defined in claim 1 is not found in the native sequence of said antigen.

In some embodiments the sequence of amino acids defined by X1-X2-X3-X4-X5 of formula I as defined in claim 1 is not found in the native sequence of said antigen.

In some embodiments the peptide is demonstrated to translocate across a plasma membrane in the assay based on biotinylation of peptides as described in example 1.

In some embodiments the 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof, is a basic amino acid.

In some embodiments the 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof, is tryptophan, or a derivative thereof.

In some embodiments the 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof, is citrulline, or a derivative thereof.

In some embodiments the one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof is selected from Arg, Lys, and His.B).

In some embodiments the one optional amino acid selected from a basic amino acid, citrulline, tryptophan or a derivative thereof is tryptophan, or a derivative thereof.

In some embodiments the one optional amino acid selected from a basic amino acid, citrulline, tryptophan or a derivative thereof is citrulline, or a derivative thereof.

In some embodiments X2 and/or X4 defines a sequence identical to the native sequence of said antigen.

In some embodiments the peptide is capable of inducing a T-lymphocyte response.

In some embodiments the peptide is capable of inducing a CD4+ and/or a CD8+ T-lymphocyte response.

In some embodiments the antigen is a viral protein, such as a capsid protein.

In some embodiments the viral protein is selected from a protein of the Hepatitis C virus, such as a core protein; protein of influenza virus, such as an M2 protein.

In some embodiments the viral protein of Hepatitis C virus is selected from HCV consensus sequence of genotype 1, such as subtypes 1a and 1b, genotype 2 such as 2a and 2b and genotype 3, such as 3a.

In some embodiments the cell-penetrating peptide is of 19-60 amino acids, such as of 20-60 amino acids, such as of 21-60 amino acids, such as of 22-60 amino acids, such as of 23-60 amino acids, such as of 24-60 amino acids, such as of 25-60 amino acids, such as of 26-60 amino acids, such as of 27-60 amino acids, such as of 28-60 amino acids, such as of 29-60 amino acids, such as of 30-60 amino acids, such as of 31-60 amino acids, such as of 32-60 amino acids, such as of 33-60 amino acids, such as of 34-60 amino acids, such as of 35-60 amino acids.

In some embodiments the cell-penetrating peptide is of 18-60 amino acids, such as 18-59 amino acids, such as 18-58 amino acids, such as 18-57 amino acids, such as 18-56 amino acids, such as 18-55 amino acids, such as 18-54 amino acids, such as 18-53 amino acids, such as 18-52 amino acids, such as 18-51 amino acids, such as 18-50 amino acids, such as 18-49 amino acids, such as 18-48 amino acids, such as 18-47 amino acids, such as 18-46 amino acids, such as 18-45 amino acids, such as 18-44 amino acids, such as 18-43 amino acids, such as 18-42 amino acids, such as 18-41 amino acids, such as 18-40 amino acids, such as 18-39 amino acids, such as 18-38 amino acids, such as 18-37 amino acids, such as 18-35 amino acids, such as of 18-34 amino acids, such as of 18-33 amino acids, such as of 18-32 amino acids, such as of 18-31 amino acids, such as of 18-30 amino acids, such as of 18-29 amino acids, such as of 18-28 amino acids, such as of 18-27 amino acids, such as of 18-26 amino acids, such as of 18-25 amino acids, such as of 18-24 amino acids, such as of 18-23 amino acids, such as of 18-22 amino acids, such as of 18-21 amino acids, such as of 18-20 amino acids, such as of 18-19 amino acids.

In some embodiments the net charge of X2 is below or equal to 0.

In some embodiments the net charge of X2 is below or equal to 0; and X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some embodiments the net charge of X2 is below or equal to 0; and the net charge of X4 is above or equal to 1.

In some embodiments the net charge of X2 is below or equal to 0; the net charge of X4 is above or equal to 1; and X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some embodiments the net charge of X2 and X4 are below or equal to 0.

In some embodiments the net charge of X2 and X4 are below or equal to 0; and X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some embodiments the net charge of X2 and X4 are above or equal to 1.

In some embodiments the net charge of X2 and X4 are above or equal to 1 and X1 and X3 defines a sequence of 1 or 2 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some embodiments the net charge of X2 is above or equal to 1; and the net charge of X4 is below or equal to 0.

In some embodiments the net charge of X2 is above or equal to 1; the net charge of X4 is below or equal to 0; X1 defines a sequence of 1 or 2 amino acids with a positive charge; and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

In some embodiments the basic amino acid is independently selected from Arg, Lys, and His.

In some embodiments X2 and/or X4 comprises the sequence of amino acids defined by position 135-157 of SEQ ID NO:3, or a fragment or variant thereof.

In some embodiments X2 and/or X4 consist of a sequence selected from GYIPLVGAPLG, GYLPAVGAPIG, GYLPAVGAPI, NYVTGNIPG, NYATGNLPG, NYATGNLPG, VTGNIPGSTYS, IRNLGRVIETLTG, SRNLGKVIDTLTC, IRNLGRVIETLT, GGGQIIGGNYLIP, GGGQIVGGVYLLP, LIFLARSALIV, LIFLARSALIL, LIFLARSALIL, SAYERMCNIL, SAYERZVNIL, TAYERZCNIL, IAYERMCNIL, IAYERMCNIL, LFFKCIYRLFKHGL, LFFKTITRLFBHGL, GLEPLVIAGILA, GSDPLVVAASIV, NLVPMVATV, NLVPMVATV, NIVPZVVTA, PEVIPMFSALS, FIIPXFTALSG, ALGPAATL, GPVVHLTL, LECVYCKQQLL, GVYDFAFRDLC, GVFDYAFRDIN, GATPVDLLGA, GVTPAGLIGV, VARALAHGVRV, VIRVIAHGLRL, GITFSIFLIVS, CSFSIFLLAL, GCSFSIFLLAL, GITFSIYLIVS, LZGYIPLIGA, LMGYIPLVGA, LZGYIPLIGA, PBIGVRATB, GPRLGVRATR, GPRLGVRAT, RGSVAHKS, SALILRGSVAHK, FQTAAQRAMM, FQTAAQRAVZ, FQTVVQBA, FQTAAQRA, GPSTEGVPESM, LLSTEGVPNSZ, GSLVGLLHIVL, ASIVGILHLIL, NLVPMVATV, NIVPZVVTA, TPQDLNTMLN, ALLYGATPYAIG, MMTACQGVG, GQAGDDFS, EVYDFAFRDLC, GFAFRDLCIVY, GFAYRDINLAY, GALNLCLPM, and GALQIBLPL, IRNLGRVIETLTLZGYIPLIGA, or a fragment or variant thereof.

In some embodiments X2 and/or X4 consist of a sequence derived from an amino acid sequence selected from SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, SEQ ID NO:31, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO:46, SEQ ID NO:126, and SEQ ID NO:198, or a fragment or variant thereof.

In some embodiments the peptide according to the invention is selected from RRGYIPLVGAPLGBGRVARALAHGVRV, RGYIPLVGAPLGRRVARALAHGVRV, RGYIPLVGAPLGRRRVARALAHGVRVR, RRGYIPLVGAPLGRRVARALAHGVRV, RRGYIPLVGAPLGRRRVARALAHGVRV, BRGYIPLVGAPLGRRVARALAHGVRV, RRRGYIPLVGAPLGBRVARALAHGVRV, RGYIPLVGAPLGKKKVARALAHGVRV, RGYIPLVGAPLGRRRVARALAHGVRV, KKGYIPLVGAPLGKKVARALAHGVRV, WGYIPLVGAPLGRRVARALAHGVRV, WWGYIPLVGAPLGRRVARALAHGVRV, EEGYIPLVGAPLGEEVARALAHGVRV, GGGYIPLVGAPLGGGVARALAHGVRV, EEGYIPLVGAPLGRRVARALAHGVRV, RRGYIPLVGAPLGLRRVARALAHGVRV, WWGYIPLVGAPLGRRVARALAHGVRV, WWGYIPLVGAPLGRRRVARALAHGVRV, WWGYIPLVGAPLGRVARALAHGVRV, RGYIPLVGAPLGRRVARALAHGVRV, RRGYLPAVGAPIGBRVIRVIAHGLRL, RRGYIPLVGAPLGBRVARALAHGVRV, GYIPLVGAPLGGVARALAHGVRV, WWGYLPAVGAPIRRVIRVIAHGLRL, GYIPLVGAPLGGVARALAHGVRV, RRGYIPLVGAPLGBGRVARALAHGVRV, RGYIPLVGAPLGRRVARALAHGVRV, RGYIPLVGAPLGRRRVARALAHGVRV, RRGYIPLVGAPLGRRVARALAHGVRV, RRGYIPLVGAPLGRRRVARALAHGVRV, BRGYIPLVGAPLGRRVARALAHGVRV, RRRGYIPLVGAPLGBRVARALAHGVRV, RGYIPLVGAPLGKKKVARALAHGVRV, RGYIPLVGAPLGRRRVARALAHGVRV, KKGYIPLVGAPLGKKVARALAHGVRV, WGYIPLVGAPLGRRVARALAHGVRV, WWGYIPLVGAPLGRRVARALAHGVRV, RRGYIPLVGAPLGLRRVARALAHGVRV, RRNYVTGNIPGBRGITFSIFLIVS, WWNYATGNLPGRRCSFSIFLLAL, WWNYVTGNIPGBRGITFSIFLIVS, WWNYVTGNIPGRRGITFSIFLIVS, RRNYATGNLPGRRGCSFSIFLLAL, RRVTGNIPGSTYSGBRGITFSIYLIVS, RRIRNLGRVIETLTGBRLZGYIPLIGA, RRSRNLGKVIDTLTCBRLMGYIPLVGA, SRN LGKVIDTLTCGFADLMGYIPLVGA, WWI RNLGRVIETLTRRLZGYIPLIGA, WWSRNLGKVIDTLTCRRLMGYIPLVGA, RRGGGQIIGGNYLIPRBPBIGVRATB, GGGQIVGGVYLLPRRGPRLGVRATR, RRGGGQIVGGVYLLPRRGPRLGVRATR, WWGGGQIVGGVYLLPRRGPRLGVRAT, BRLIFLARSALIVRGSVAHKS, EDLIFLARSALILRGSVAHKS, BRLIFLARSALILBGRSALILRGSVAHK, SAYERMCNILKGKFQTAAQRAMM, SAYERZVNILKGKFQTAAQRAVZ, BRTAYERZCNILBRGRFQTVVQBA, BRIAYERMCNILLBRGKFQTAAQRA, IAYERMCNILKGKFQTAAQRA, LFFKCIYRLFKHGLKRGPSTEGVPESM, BRRLFFKTITRLFBHGLRRLLSTEGVPNSZ, BRGLEPLVIAGILARRGSLVGLLHIVL, BRGSDPLVVAASIVRRASIVGILHLIL, RNLVPMVATVRRNLVPMVATVB, RNLVPMVATVBRRNLVPMVATVB, RNIVPZVVTARRNIVPZVVTAB, PEVIPMFSALSEGATPQDLNTMLN, RFIIPXFTALSGGRRALLYGATPYAIG, KALGPAATLEEMMTACQGVG, RRGPVVHLTLRRRGQAGDDFS, RRGPVVHLTLRRRGQAGDDFS, RRGPVVHLTLRGRRGQAGDDFS, RRLECVYCKQQLLRREVYDFAFRDLC, RRGVYDFAFRDLCRRGFAFRDLCIVYR, RRGVFDYAFRDINRRGFAYRDINLAYR, RRGATPVDLLGARRGALNLCLPMR, RRGVTPAGLIGVRRGALQIBLPLR, RGYLPAVGAPIGRRRVIRVIAHGLRLR, RRSRNLGKVIDTLTCRRLMGYIPLVGA, RRIRNLGRVIETLTLZGYIPLIGARRIRNLGRVIETLTLZGYIPLIGAR, or a fragment or variant thereof.

In some embodiments the peptide consist of a sequence selected from X1-NYVTGNIPG-X3-GITFSIYLIVS; X1-IRNLGRVIETLT-X3-LZGYIPLIGA; X1-GYLPAVGAPI-X3-VIRVIAHGLRL; X1-GGGQIIGGNYLIP-X3-PBIGVRATB; X1-NYATGNLPG-X3-GCSFSIFLLAL; X1-SRNLGKVIDTLTC-X3-LMGYIPLVGA; X1-GYIPLVGAPL-X3-VARALAHGVRV; X1-GGGQIVGGVYLLP-X3-PRLGVRATR; X1-LTFLVRSVLLI-X3-GSVLIVRGSLVH; X1-TAYERZCNIL-X3-GRFQTVVQBA; X1-SDPLVVAASIV-X3-ASIVGILHLIL; X1-LIFLARSALIL-X3-SALILRGSVAH; X1-IAYERMCNIL-X3-GKFQTAAQRA; and X1-LEPLVIAGILA-X3-GSLVGLLHIVL; X1-NLVPMVATV-X3-NLVPMATV; X1-GYLPAVGAPIG-X3-VIRVIAHGLRL; X1-IRNLGRVIETLTG-X3-LZGYIPLIGA; X1-GVYDFAFRDLC-X3-GFAFRDLCIVYR, X1-GVFDYAFRDIN-X3-GFAYRDINLAYR, X1-GATPVDLLGA-X3-GALNLCLPMR, X1-GVTPAGLIGV-X3-GALQIBLPLR, and X1-IRNLGRVIETLTLZGYIPLIGA-X3-IRNLGRVIETLTLZGYIPLIGA; optionally with an X5 in the C-terminal of the peptide wherein X1, X3 and X5 refers to X1, X3, and X5 of formula I.

In some embodiments the peptide comprises one or more cysteine.

In some embodiments the peptide contain intramolecular bonds, such as intramolecular disulfide (S—S) bonds between two cys residues.

In other embodiments the peptide contains intramolecular bonds, such as in the form of a acylal moiety (COO—CH2-OOC, COO—CHR—OOC or COO—CR2-OOC).

In some embodiments the N- and/or C-terminal amino acid in X2 is a hydrophilic or polar amino acid.

In some embodiments the N-terminal amino acid in X4 is a hydrophilic or polar amino acid.

In some embodiments the peptide according to the invention is not more than 58 amino acids, such as not more than 56, 54, 52, 50, 48, 46, 44, 42, 40, 38, 36, 34, 32, 30, 28, 26, 24, 22, 20, 18 amino acid residues.

In some embodiments X1 consist of 2 or 3 amino acids.

In some embodiments X1 consist of WW, BR, or RR.

In some embodiments X1 consist of R, or W.

In some embodiments X3 consist of 2 or 3 amino acids.

In some embodiments X3 consist of WW, BR, or RR.

In some embodiments X3 consist of RRR, BRR, or BRGR.

In some embodiments an isolated peptide according to the invention consists of a sequence of X2 or X4 as defined in table 1 or in table 2.

In some embodiments an isolated peptide according to the invention comprises a sequence of X2 and/or X4 as defined in table 1 or in table 2, or a fragment thereof.

In some embodiments X2 defines a sequence of 8-25 amino acids, such as 8-20 amino acids, such as 8-15 amino acids, such as 8-11 amino acids.

In some embodiments X2 defines a sequence of less than 25, such as less than 24, 23, 22, 21, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7 or 6 amino acids.

In some embodiments X2 defines a sequence of more than 8, such as more than 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 amino acids.

In some embodiments X4 defines a sequence of 8-25 amino acids, such as 8-20 amino acids, such as 8-15 amino acids, such as 8-11 amino acids.

In some embodiments X4 defines a sequence of less than 25, such as less than 24, 23, 22, 21, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7 or 6 amino acids.

In some embodiments X4 defines a sequence of more than 8, such as more than 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 amino acids.

In some embodiments the dimer peptide according to the invention consist of two identical peptide monomers.

In some embodiments the immunogenic composition according to the invention is in the form of a vaccine composition.

In some embodiments, the cell-penetrating peptide of the invention comprises at most 60, at most 59, at most 58, at most 57, at most 56, at most 55, at most 54, at most 53, at most 52, at most 51, at most 50, at most 49, at most 48, at most 47, at most 46, at most 45, at most 44, at most 43, at most 42, at most 41, at most 40, at most 39, at most 38, at most 37, at most 36, at most 35, at most 34, at most 33, at most 32, at most 31, at most 30, at most 29, at most 28, at most 27, at most 26, at most 25, at most 24, at most 23, at most 22, at most 21, at most 20, at most 19, at most 18 amino acids.

In some embodiments, the cell-penetrating peptide of the invention comprises at least 18, at least 19, at least 20, at least 21, at least 22, at least 23, at least 24, at least 25, at least 26, at least 27, at least 28, at least 29, at least 30, at least 31, at least 32, at least 33, at least 34, at least 35 at least 36, at least 37, at least 38, at least 39, at least 40, at least 41, at least 42, at least 43, at least 44, at least 45, at least 46, at least 47, at least 48, at least 49, at least 50, at least 51, at least 52, at least 53, at least 54, at least 55, at least 56, at least 57, at least 58, at least 59, at least 60 amino acid residues.

In some embodiments, the cell-penetrating peptide of the invention consists of 18 amino acid residues or 19 amino acid residues or 20 amino acid residues or 21 amino acid residues or 22 amino acid residues or 23 amino acid residues or 24 amino acid residues or 25 amino acid residues or 26 amino acid residues or 27 amino acid residues or 28 amino acid residues or 29 amino acid residues or 30 amino acid residues or 31 amino acid residues or 32 amino acid residues or 33 amino acid residues or 34 amino acid residues or 35 amino acid residues or 36 amino acid residues or 37 amino acid residues or 38 amino acid residues or 39 amino acid residues or 40 amino acid residues or 41 amino acid residues or 42 amino acid residues or 43 amino acid residues or 44 amino acid residues or 45 amino acid residues or 46 amino acid residues or 47 amino acid residues or 48 amino acid residues or 49 amino acid residues or 50 amino acid residues or 51 amino acid residues or 52 amino acid residues or 53 amino acid residues or 54 amino acid residues or 55 amino acid residues or 56 amino acid residues or 57 amino acid residues or 58 amino acid residues or 59 amino acid residues or 60 amino acid residues.

In some embodiments the cell-penetrating peptide of the invention does not consist of the following sequence RFIIP[Nle]FTALSGGRRALLYGATPYAIG, where Nle denotes a nor-leucine.

In some embodiments X2 and/or X4 is not derived from HIV.

In some embodiments X4 is a linear sequence of less than 12 amino acids.

In some embodiments X2 is a linear sequence of less than 12 amino acids.

In some embodiments X2 and/or X4 do not contain nor-leucine.

In some embodiments X2 do not contain nor-leucine.

In some embodiments X2 and/or X4 only contains natural amino acids.

In some embodiments X2 only contains natural amino acids.

In some embodiments X2 only contains natural amino acids if derived from HIV. In some embodiments X2 and/or X4 is derived from HCV, CMV, HPV, Influenza, adenoviruses, or picornaviruses.

Numbered embodiments according to the invention:

1. An isolated cell-penetrating peptide comprising the following structure


X1-X2-X3-X4-X5  (formula I),

wherein X1 and X3 independently defines a linear sequence of any 1, 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof; X2 defines a linear sequence of 8-30 amino acids derived from an antigen; X4 defines a linear sequence of 8-30 amino acids derived from said antigen, said sequence X4 being different from X2; and wherein X5 is any one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof.

2. The isolated peptide according to embodiment 1, wherein X1 defines a linear sequence of any 1, 2, 3, or 4 amino acids independently selected from any basic amino acid, tryptophan, or a derivative thereof.

3. The isolated peptide according to embodiment 1, wherein X1 defines a linear sequence in any order of one citrulline and any 1, 2, or 3 amino acids independently selected from any basic amino acid, tryptophan, or a derivative thereof.

4. The isolated peptide according to any one of embodiment 1-3, wherein X3 defines a linear sequence of any 1, 2, 3, or 4 amino acids independently selected from any basic amino acid.

5. The isolated peptide according to any one of embodiment 1-3, wherein X3 defines a linear sequence in any order of one citrulline and of any 1, 2, or 3 amino acids independently selected from any basic amino acid.

6. The isolated peptide according to any one of embodiment 1-5, wherein the sequence of amino acids defined by X2-X3-X4 of formula I as defined in embodiment 1 is not found in the native sequence of said antigen.

7. The isolated peptide according to any one of embodiment 1-6, wherein said peptide is demonstrated to translocate across a plasma membrane in the assay based on biotinylation of peptides as described in example 1.

8. The isolated peptide according to any one of embodiments 1-7, wherein said one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof is selected from Arg, Lys, and His.

9. The isolated peptide according to any one of embodiments 1-8, wherein X2 and/or X4 defines a sequence identical to the native sequence of said antigen.

10. The isolated peptide according to any one of embodiments 1-9, wherein said peptide is capable of inducing a T lymphocyte response.

11. The isolated peptide according to any one of embodiments 1-10, wherein said antigen is a viral protein, such as a capsid protein.

12. The isolated peptide according to embodiment 11, wherein said viral protein is selected from a protein of the Hepatitis C virus, such as a core protein; protein of influenza virus, such as an M2 protein.

13. The isolated peptide according to embodiment 11, wherein said viral protein of Hepatitis C virus is selected from HCV consensus sequence of genotype 1, such as subtypes 1a and 1b, genotype 2 such as 2a and 2b and genotype 3, such as 3a.

14. The isolated peptide according to any one of embodiments 1-13, which cell-penetrating peptide is of 19-60 amino acids, such as of 20-60 amino acids, such as of 21-60 amino acids, such as of 22-60 amino acids, such as of 23-60 amino acids, such as of 24-60 amino acids, such as of 25-60 amino acids, such as of 26-60 amino acids, such as of 27-60 amino acids, such as of 28-60 amino acids, such as of 29-60 amino acids, such as of 30-60 amino acids, such as of 31-60 amino acids, such as of 32-60 amino acids, such as of 33-60 amino acids, such as of 34-60 amino acids, such as of 35-60 amino acids.

15. The isolated peptide according to any one of embodiments 1-14, which cell-penetrating peptide is of 18-60, such as 18-59, such as 18-58, such as 18-57, such as 18-56, such as 18-55, such as 18-54, such as 18-53, such as 18-52, such as 18-51, such as 18-50, such as 18-49, such as 18-48, such as 18-47, such as 18-46, such as 18-45, such as 18-44, such as 18-43, such as 18-42, such as 18-41, such as 18-40, such as 18-39, such as 18-38, such as 18-37, such as 18-35 amino acids, such as of 18-34 amino acids, such as of 18-33 amino acids, such as of 18-32 amino acids, such as of 18-31 amino acids, such as of 18-30 amino acids, such as of 18-29 amino acids, such as of 18-28 amino acids, such as of 18-27 amino acids, such as of 18-26 amino acids, such as of 18-25 amino acids, such as of 18-24 amino acids, such as of 18-23 amino acids, such as of 18-22 amino acids, such as of 18-21 amino acids, such as of 18-20 amino acids, such as of 18-19 amino acids.

16. The isolated peptide according to any one of embodiments 1-15, wherein the net charge of X2 is below or equal to 0; and wherein X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

17. The isolated peptide according to any one of embodiments 1-16, wherein the net charge of X2 is below or equal to 0; wherein the net charge of X4 is above or equal to 1; and wherein X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

18. The isolated peptide according to any one of embodiments 1-17, wherein the net charge of X2 and X4 are below or equal to 0 and wherein X1 and X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

19. The isolated peptide according to any one of embodiments 1-18, wherein the net charge of X2 and X4 are above or equal to 1 and wherein X1 and X3 defines a sequence of 1 or 2 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

20. The isolated peptide according to any one of embodiments 1-19, wherein the net charge of X2 is above or equal to 1; wherein the net charge of X4 is below or equal to 0; wherein X1 defines a sequence of 1 or 2 amino acids with a positive charge; and wherein X3 defines a sequence of 2, 3 or 4 amino acid independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof.

21. The isolated peptide according to any one of embodiments 1-20, wherein said basic amino acid is independently selected from Arg, Lys, and His.

22. The isolated peptide according to any one of embodiments 1-21, wherein X2 and/or X4 comprises the sequence of amino acids defined by position 135-157 of SEQ ID NO:3, or a fragment or variant thereof.

23. The isolated peptide according to any one of embodiments 1-22, wherein X2 and/or X4 consist of a sequence selected from GYIPLVGAPLG, GYLPAVGAPIG, GYLPAVGAPI, NYVTGNIPG, NYATGNLPG, NYATGNLPG, VTGNIPGSTYS, IRNLGRVIETLTG, SRNLGKVIDTLTC, IRNLGRVIETLT, GGGQIIGGNYLIP, GGGQIVGGVYLLP, LIFLARSALIV, LIFLARSALIL, LIFLARSALIL, SAYERMCNIL, SAYERZVNIL, TAYERZCNIL, IAYERMCNIL, IAYERMCNIL, LFFKCIYRLFKHGL, LFFKTITRLFBHGL, GLEPLVIAGILA, GSDPLVVAASIV, NLVPMVATV, NLVPMVATV, NIVPZVVTA, PEVIPMFSALS, FIIPXFTALSG, ALGPAATL, GPVVHLTL, LECVYCKQQLL, GVYDFAFRDLC, GVFDYAFRDIN, GATPVDLLGA, GVTPAGLIGV, VARALAHGVRV, VIRVIAHGLRL, GITFSIFLIVS, CSFSIFLLAL, GCSFSIFLLAL, GITFSIYLIVS, LZGYIPLIGA, LMGYIPLVGA, LZGYIPLIGA, PBIGVRATB, GPRLGVRATR, GPRLGVRAT, RGSVAHKS, SALILRGSVAHK, FQTAAQRAMM, FQTAAQRAVZ, FQTVVQBA, FQTAAQRA, GPSTEGVPESM, LLSTEGVPNSZ, GSLVGLLHIVL, ASIVGILHLIL, NLVPMVATV, NIVPZVVTA, TPQDLNTMLN, ALLYGATPYAIG, MMTACQGVG, GQAGDDFS, EVYDFAFRDLC, GFAFRDLCIVY, GFAYRDINLAY, GALNLCLPM, GALQIBLPL, and IRNLGRVIETLTLZGYIPLIGA, or a fragment or variant thereof.

24. The isolated peptide according to any one of embodiments 1-23, wherein X2 and/or X4 consist of a sequence derived from an amino acid sequence selected from SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, SEQ ID NO:31, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO:46, SEQ ID NO:126, and SEQ ID NO:198, or a fragment or variant thereof.

25. The isolated peptide according to any one of embodiments 1-24, wherein said peptide is selected from RRGYIPLVGAPLGBGRVARALAHGVRV (SEQ ID NO:47), RGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:48), RGYIPLVGAPLGRRRVARALAHGVRVR (SEQ ID NO:49), RRGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:50), RRGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:51), BRGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:52), RRRGYIPLVGAPLGBRVARALAHGVRV (SEQ ID NO:53), RGYIPLVGAPLGKKKVARALAHGVRV (SEQ ID NO:54), RGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:55), KKGYIPLVGAPLGKKVARALAHGVRV (SEQ ID NO:56), WGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:57), WWGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:58), EEGYIPLVGAPLGEEVARALAHGVRV (SEQ ID NO:59), GGGYIPLVGAPLGGGVARALAHGVRV (SEQ ID NO:60), EEGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:61), RRGYIPLVGAPLGLRRVARALAHGVRV (SEQ ID NO:62), WWGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:63), WWGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:64), WWGYIPLVGAPLGRVARALAHGVRV (SEQ ID NO:65), RGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:66), RRGYLPAVGAPIGBRVIRVIAHGLRL (SEQ ID NO:67), RRGYIPLVGAPLGBRVARALAHGVRV (SEQ ID NO:68), GYIPLVGAPLGGVARALAHGVRV (SEQ ID NO:69), WWGYLPAVGAPIRRVIRVIAHGLRL (SEQ ID NO:70), GYIPLVGAPLGGVARALAHGVRV (SEQ ID NO:71), RRGYIPLVGAPLGBGRVARALAHGVRV (SEQ ID NO:72), RGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:73), RGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:74), RRGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:75), RRGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:76), BRGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:77), RRRGYIPLVGAPLGBRVARALAHGVRV (SEQ ID NO:78), RGYIPLVGAPLGKKKVARALAHGVRV (SEQ ID NO:79), RGYIPLVGAPLGRRRVARALAHGVRV (SEQ ID NO:80), KKGYIPLVGAPLGKKVARALAHGVRV (SEQ ID NO:81), WGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:82), WWGYIPLVGAPLGRRVARALAHGVRV (SEQ ID NO:83), RRGYIPLVGAPLGLRRVARALAHGVRV (SEQ ID NO:84), RRNYVTGNIPGBRGITFSIFLIVS (SEQ ID NO:85), WWNYATGNLPGRRCSFSIFLLAL (SEQ ID NO:86), WWNYVTGNIPGBRGITFSIFLIVS (SEQ ID NO:87), WWNYVTGNIPGRRGITFSIFLIVS (SEQ ID NO:88), RRNYATGNLPGRRGCSFSIFLLAL (SEQ ID NO:89), RRVTGNIPGSTYSGBRGITFSIYLIVS (SEQ ID NO:90), RRIRNLGRVIETLTGBRLZGYIPLIGA (SEQ ID NO:91), RRSRNLGKVIDTLTCBRLMGYIPLVGA (SEQ ID NO:92), SRNLGKVIDTLTCGFADLMGYIPLVGA (SEQ ID NO:93), WWIRNLGRVIETLTRRLZGYIPLIGA (SEQ ID NO:94), WWSRNLGKVIDTLTCRRLMGYIPLVGA (SEQ ID NO:95), RRGGGQIIGGNYLIPRBPBIGVRATB (SEQ ID NO:96), GGGQIVGGVYLLPRRGPRLGVRATR (SEQ ID NO:97), RRGGGQIVGGVYLLPRRGPRLGVRATR (SEQ ID NO:98), WWGGGQIVGGVYLLPRRGPRLGVRAT (SEQ ID NO:99), BRLIFLARSALIVRGSVAHKS (SEQ ID NO:100), EDLIFLARSALILRGSVAHKS (SEQ ID NO:101), BRLIFLARSALILBGRSALILRGSVAHK (SEQ ID NO:102), SAYERMCNILKGKFQTAAQRAMM (SEQ ID NO:103), SAYERZVNILKGKFQTAAQRAVZ (SEQ ID NO:104), BRTAYERZCNILBRGRFQTVVQBA (SEQ ID NO:105), BRIAYERMCNILLBRGKFQTAAQRA (SEQ ID NO:106), IAYERMCNILKGKFQTAAQRA (SEQ ID NO:107), LFFKCIYRLFKHGLKRGPSTEGVPESM (SEQ ID NO:108), BRRLFFKTITRLFBHGLRRLLSTEGVPNSZ (SEQ ID NO:109), BRGLEPLVIAGILARRGSLVGLLHIVL (SEQ ID NO:110), BRGSDPLVVAASIVRRASIVGILHLIL (SEQ ID NO:111), RNLVPMVATVRRNLVPMVATVB (SEQ ID NO:112), RNLVPMVATVBRRNLVPMVATVB (SEQ ID NO:113), RNIVPZVVTARRNIVPZVVTAB (SEQ ID NO:114), PEVIPMFSALSEGATPQDLNTMLN (SEQ ID NO:115), RFIIPXFTALSGGRRALLYGATPYAIG (SEQ ID NO:116), KALGPAATLEEMMTACQGVG (SEQ ID NO:117), RRGPVVHLTLRRRGQAGDDFS (SEQ ID NO:118), RRGPVVHLTLRRRGQAGDDFS (SEQ ID NO:119), RRGPVVHLTLRGRRGQAGDDFS (SEQ ID NO:120), RRLECVYCKQQLLRREVYDFAFRDLC (SEQ ID NO:121), RRGVYDFAFRDLCRRGFAFRDLCIVYR (SEQ ID NO:122), RRGVFDYAFRDINRRGFAYRDINLAYR (SEQ ID NO:123), RRGATPVDLLGARRGALNLCLPMR (SEQ ID NO:124), RRGVTPAGLIGVRRGALQIBLPLR (SEQ ID NO:125), RGYLPAVGAPIGRRRVIRVIAHGLRLR (SEQ ID NO:196), RRSRNLGKVIDTLTCRRLMGYIPLVGA (SEQ ID NO:197), and RRIRNLGRVIETLTLZGYIPLIGARRIRNLGRVIETLTLZGYIPLIGAR (SEQ ID NO:199), or a fragment or variant thereof.

26. The isolated peptide according to any one of embodiments 1-25, wherein the peptide consist of a sequence selected from X1-NYVTGNIPG-X3-GITFSIYLIVS; X1-IRNLGRVIETLT-X3-LZGYIPLIGA; X1-GYLPAVGAPI-X3-VIRVIAHGLRL; X1-GGGQIIGGNYLIP-X3-PBIGVRATB; X1-NYATGNLPG-X3-GCSFSIFLLAL; X1-SRNLGKVIDTLTC-X3-LMGYIPLVGA; X1-GYIPLVGAPL-X3-VARALAHGVRV; X1-GGGQIVGGVYLLP-X3-PRLGVRATR; X1-LTFLVRSVLLI-X3-GSVLIVRGSLVH; X1-TAYERZCNIL-X3-GRFQTVVQBA; X1-SDPLVVAASIV-X3-ASIVGILHLIL; X1-LIFLARSALIL-X3-SALILRGSVAH; X1-IAYERMCNIL-X3-GKFQTAAQRA; and X1-LEPLVIAGILA-X3-GSLVGLLHIVL; X1-NLVPMVATV-X3-NLVPMATV; X1-GYLPAVGAPIG-X3-VIRVIAHGLRL; X1-IRNLGRVIETLTG-X3-LZGYIPLIGA; X1-GVYDFAFRDLC-X3-GFAFRDLCIVYR, X1-GVFDYAFRDIN-X3-GFAYRDINLAYR, X1-GATPVDLLGA-X3-GALNLCLPMR, X1-GVTPAGLIGV-X3-GALQIBLPLR, and X1-IRNLGRVIETLTLZGYIPLIGA-X3-IRNLGRVIETLTLZGYIPLIGA; optionally with an X5 in the C-terminal of the peptide, wherein X1 and X3 and X5 refers to X1, X3, and X5 of formula I.

27. The isolated peptide according to any one of embodiments 1-26, wherein the peptide comprises one or more cysteine.

28. The isolated peptide according to any one of embodiments 1-27, wherein the peptide contain intramolecular bonds, such as intramolecular disulfide (S—S) bonds between two cys residues or acylals.

29. The isolated peptide according to any one of embodiments 1-28, wherein the N- and/or C-terminal amino acid in X2 is a hydrophilic or polar amino acid.

30. The isolated peptide according to any one of embodiments 1-29, wherein the N-terminal amino acid in X4 is a hydrophilic or polar amino acid.

31. The isolated peptide according to any one of embodiments 1-30, which is not more than 58 amino acids, such as not more than 56, 54, 52, 50, 48, 46, 44, 42, 40, 38, 36, 34, 32, 30, 28, 26, 24, 22, 20, 18 amino acid residues.

32. The isolated peptide according to any one of embodiments 1-31, wherein X1 consist of 2 or 3 amino acids.

33. The isolated peptide according to embodiment 32, wherein X1 consist of WW, BR, or RR.

34. The isolated peptide according to any one of embodiments 1-33, wherein X3 consist of 2 or 3 amino acids.

35. The isolated peptide according to embodiment 34, wherein X3 consist of WW, BR, or RR.

36. Isolated peptide of not more than 60 amino acids comprising a sequence of X2 and/or X4 as independently defined in any one of table 1 or table 2.

37. Isolated peptide according to embodiment 36, which peptide consists of a sequence of X2 or X4 as independently defined in any one of table 1 or table 2.

38. The isolated peptide according to any one of embodiments 1-37, wherein X2 defines a sequence of 8-25 amino acids, such as 8-20 amino acids, such as 8-15 amino acids.

39. The isolated peptide according to any one of embodiments 1-38, wherein X4 defines a sequence of 8-25 amino acids, such as 8-20 amino acids, such as 8-15 amino acids.

40. The isolated peptide according to any one of embodiments 1-39, wherein X2 defines a sequence of less than 25, such as less than 24, 23, 22, 21, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7 or 6 amino acids.

41. The isolated peptide according to any one of embodiments 1-40, wherein X2 defines a sequence of more than 8, such as more than 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 amino acids.

42. The isolated peptide according to any one of embodiments 1-41, wherein X4 defines a sequence of less than 25, such as less than 24, 23, 22, 21, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7 or 6 amino acids.

43. The isolated peptide according to any one of embodiments 1-42, wherein X4 defines a sequence of more than 8, such as more than 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 amino acids.

44. The isolated peptide according to any one of embodiments 1-43, wherein the cell-penetrating peptide of the invention does not consist of the following sequence RFIIP[Nle]FTALSGGRRALLYGATPYAIG, where Nle denotes a nor-leucine.

45. The isolated peptide according to any one of embodiments 1-44, wherein X2 and/or X4 is not derived from HIV.

46. The isolated peptide according to any one of embodiments 1-45, wherein X4 is a linear sequence of less than 12 amino acids.

47. The isolated peptide according to any one of embodiments 1-46, wherein X2 is a linear sequence of less than 12 amino acids.

48. The isolated peptide according to any one of embodiments 1-47, wherein X2 and/or X4 do not contain nor-leucine.

49. The isolated peptide according to any one of embodiments 1-48, wherein X2 do not contain nor-leucine.

50. The isolated peptide according to any one of embodiments 1-49, wherein X2 and/or X4 only contains natural amino acids.

51. The isolated peptide according to any one of embodiments 1-50, wherein X2 only contains natural amino acids.

52. The isolated peptide according to any one of embodiments 1-51, wherein X2 only contains natural amino acids if derived from HIV.

53. The isolated peptide according to any one of embodiments 1-52, wherein X2 and/or X4 is derived from HCV, CMV, HPV, Influenza, adenoviruses, or picornaviruses.

54. Use of a peptide comprising a sequence of X2 or X4 as independently defined in any one of table 1 or table 2 for inducing an immune response in a subject.

55. A dimer peptide comprising two peptides monomers, wherein each peptide monomer is as defined in any one of embodiments 1-53.

56. A dimer peptide according to embodiment 55, wherein the two peptide monomers are identical.

57. Peptide combination comprising two or more peptide according to any one of embodiments 1-53.

58. An isolated nucleic acid or polynucleotide encoding a peptide according to any one of embodiments 1-53.

59. A vector comprising the nucleic acid or polynucleotide according to embodiment 58.

60. A host cell comprising the vector according to embodiment 59.

61. An immunogenic composition comprising at least one peptide according to any one of embodiments 1-53, a dimer peptide according to any one of embodiments 55-56, a peptide combination according to embodiment 57, the nucleic acid or polynucleotide according to embodiment 58, or the vector according to embodiment 59; in combination with a pharmaceutically acceptable diluent or vehicle and optionally an immunological adjuvant.

62. The immunogenic composition according to embodiment 61 in the form of a vaccine composition.

63. A method for inducing an immune response in a subject against an antigen which comprises administration of at least one peptide according to any one of embodiments 1-53, a dimer peptide according to any one of embodiments 55-56, a peptide combination according to embodiment 57, the nucleic acid or polynucleotide according to embodiment 58, or the vector according to embodiment 59; or the composition according to any one of embodiments 61-62.

64. A method for reducing and/or delaying the pathological effects of a virus in a subject infected with said virus, the method comprising administering an effective amount of at least one peptide according to any one of embodiments 1-53, a dimer peptide according to any one of embodiments 55-56, a peptide combination according to embodiment 57, the nucleic acid or polynucleotide according to embodiment 58, or the vector according to embodiment 59; or the composition according to any one of embodiments 61-62.

65. A peptide according to any one of embodiments 1-53 for use as a medicament.

66. A peptide according to any one of embodiments 1-53 for treating the pathological effects of a virus in a subject infected with said virus.

Sequence list (amino acids in bold represents suitable antigenic sequences that may be used as any of X2 and/or X4 as defined in formula I of the present invention)

SEQ ID NO: 1: Accession no AF009606; Hepatitis C virus subtype  1a polyprotein gene, complete cds. MSTNPKPQRKTKANTNRRPQDVKFPGGGQIVGGVYLLPRRGPRL GVRATRKTSERSQPRGRRQPIPKARRPEGRTWAQPGYPWPLYGNEGCGWAGWLLSPRG SRPSWGPTDPARRSRNLGKVIDTLTCGFADLMGYIPLVGAPLGGAARALAHGVRVLED GVNYATGNLPGCSFSIFLLALLSCLTVPASAYQVANSSGLYHVTNDCPNSSIVYEAAD AILHTPGCVPCVREGNASRCWVAVTPTVATRDGKLPTTQLRRHIDLLVGSATLCSALY VGDLCGSVFLVGQLFTFSPRRHWTTQDCNCSIYPGHITGHRMAWDMMMNWSPTAALVV AQLLRIPQAIMDMIAGAHWGVLAGIAYFSMVGNWAKVLVVLLLFAGVDAETHVTGGSA GRTTAGLVGLLTPGAKQNIQLINTNGSWHINSTALNCNESLNTGWLAGLFYQHKFNSS GCPERLASCRALTDFAQGWGPISYANGSGLDERPYCWHYPPRPCGIVPAKSVCGPVYC FTPSPVVVGTTDRSGAPTYSWGANDTDVFVLNNTRPPLGNWFGCTWMNSTGFTKVCGA PPCVIGGVGNNTLLCPTDCFRKHPEATYSRCGSGPWITPRCMVDYPYRLWHYPCTINY TIFKVRMYVGGVEHRLEAACNWTRGERCDLEDRDRSELSPLLLSTTQWQVLPCSFTTL PALSTGLIHLHQNIVDVQYLYGVGSSIASWAIKWEYVVLLFLLLADARVCSCLWMMLL ISQAEAALENLVILNAASLAGTHGLVSFLVFFCFAWYLKGRWVPGAVYAFYGMWPLLL LLLALPQRAYALDTEVAASCGGVVLVGLMALTLSPYYKRYISWCMWWLQYFLTRVEAQ LHVWVPPLNVAGGRDAVILLMCVVHPTLVFDITKLLLAIFGPLWILQASLLKVPYFVR VQGLLRICALARKIAGGHYVQMAIIKLGALTGTYVYNHLTPLRDWAHNGLADLAVAVE PVVFSRMETKLITWGADTAACGDIINGLPVSARRGQEILLGPADGMVSKGWALLAPIT AYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATCINGVCWTVYHGAGTR TIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPCTCGSSDLYLVTRHADVIPVRARG DSRGSLLSPRPISYLKGSSGGPLLCPAGHAVGLFRAAVCTRGVAKAVDFIPVENLETT MRSPVFTDNSSPPAVPQSFQVAHLHAPTGSGKSTKVPAAYAAQGYKVLVLNPSVAATL GFGAYMSKAHGVDPNIRTGVRTITTGSPITYSTYGKFLADGGCSGGAYDIIICDECHS TDATSILGIGTVLDQAETAGARLVVLATATPPGSVTVSHPNIEEVALSTTGEIPFYGK AIPLEVIKGGRHLIFCHSKKKCDELAAKLVALGINAVAYYRGLDVSVIPTSGDVVVVS TDALMTGFTGDFDSVIDCNTCVTQTVDFSLDPTFTIETTTLPQDAVSRTQRRGRTGRG KPGIYRFVAPGERPSGMFDSSVLCECYDAGCAWYELTPAETTVALRAYMNTPGLPVCQ DHLEFWEGVFTGLTHIDAHFLSQTKQSGENFPYLVAYQATVCARAQAPPPSWDQMWKC LIRLKPTLHGPTPLLYRLGAVQNEVTLTHPITKYIMTCMSADLEVVTSTWVLVGGVLA ALAAYCLSTGCVVIVGRIVLSGKPAIIPDREVLYQEFDEMEECSQHLPYIEQGMMLAE QFKQKALGLLQTASRQAEVITPAVQTNWQKLEVFWAKHMWNFISGIQYLAGLSTLPGN PAIASLMAFTAAVTSPLTTGQTLLFNILGGWVAAQLAAPGAATAFVGAGLAGAAIGSV GLGKVLVDILAGYGAGVAGALVAFKIMSGEVPSTEDLVNLLPAILSPGALVVGVVCAA ILRRHVGPGEGAVQWMNRLIAFASRGNHVSPTHYVPESDAAARVTAILSSLTVTQLLR RLHQWISSECTTPCSGSWLRDINDWICEVLSDFKTWLKAKLMPQLPGIPFVSCQRGYR GVWRGDGIMHTRCHCGAEITGHVKNGTMRIVGPRTCRNMWSGTFPINAYTTGPCTPLP APNYKFALWRVSAEEYVEIRRVGDFHYVSGMTTDNLKCPCQIPSPEFFTELDGVALHR FAPPCKPLLREEVSFRVGLHEYPVGSQLPCEPEPDVAVLTSMLTDPSHITAEAAGRAL ARGSPPSMASSSASQLSAPSLKATCTANHDSPDAELIEANLLWRQEMGGNITRVESEN KVVILDSFDPLVAEEDEREVSVPAEILRKSARFARALPVWARPDYNPPLVETWKKPDY EPPVVHGCPLPPPRSPPVPPPRKKRTVVLTESTLSTALAELATKSFGSSSTSGITGDN TTTSSEPAPSGCPPDSDVESYSSMPPLEGEPGDPDLSDGSWSTVSSGADTEDVVCCSM SYSWTGALVTPCAAEEQKLPINALSNSLLRHHNLVYSTTSRSACQRQKKVTFDRLQVL DSHYQDVLKEVKAAASKVKANLLSVEEACSLTPPHSAKSKFGYGAKDVRCHARKAVAH INSVWKDLLEDSVTPIDTTIMAKNEVFCVQPEKGGRKPARLIVFPDLGVRVCEKMALY DVVSKLPLAVMGSSYGFQYSPGQRVEFLVQAWKSKKTPMGFSYDTRCFDSTVTESDIR TEEAIYQCCDLDPQARVAIKSLTERLYVGGPLTNSRGENCGYRRCRASGVLTTSCGNT LTCYIKARAACRAAGLQDCTMLVCGDDLVVICESAGVQEDAASLRAFTEAMTRYSAPP GDPPQPEYDLELITSCSSNVSVAHDGAGKRVYYLTRDPTTPLARAAWETARHTPVNSW LGNIIMFAPTLWARMILMTHFFSVLIARDQLEQALNCEIYGACYSIEPLDLPPIIQRL HGLSAFSLHSYSPGEINRVAACLRKLGVPPLRAWRHRARSVRARLLSRGGRAAICGKY LFNWAVRTKLKLTPIAAAGRLDLSGWFTAGYSGGDIYHSVSHARPRWFWFCLLLLAAG VGIYLLPNR SEQ ID NO: 2: HCV core protein, H77, Accession AF009606 Genbank number: 2316097 >gi|2316098|gb|AAB66324.1| polyprotein [Hepatitis C virus subtype 1a] MSTNPKPQRKTKRNTNRRPQDVKFPGGGQIVGGVYLLPRRGPRLGVRATRKTSERSQPRGRRQPIPKARR PEGRTWAQPGYPWPLYGNEGCGWAGWLLSPRGSRPSWGPTDPARRSRNLGKVIDTLTCGFADLMGYIPLV GAPLGGAARALAHGVRVLEDGVNYATGNLPGCSFSIFLLALLSCLTVPASA SEQ ID NO: 3: Hepatitis C virus mRNA, complete cds; ACCESSION M96362 M72423; Hepatitis C virus subtype 1b MSTNPKPQRKTKANTNRRPQDIKFPGGGQIVGGVYLLPRRGPRL GVRATRKTSERSQPRGRRQPIPKARRPEGRAWAQPGYPWPLYGNEGLGWAGWLLSPRG SRPSWGPTDPARKSRNLGKVIDTLTCGFADLMGYIPLVGAPLGGVARALAHGVRVLED GVNYATGNLPGCSFSIFLLALLSCLTTPVSAYEVRNASGMYHVTNDCSNSSIVYEAAD MIMHTPGCVPCVREDNSSRCWVALTPTLAARNASVPTTTLARHVDLLVGVAAFCSAMY VGDLCGSVFLVSQLFTFSPRRHETVQDCNCSIYPGRVSGHRMAWDMMMNWSPTTALVV SQLLRIPQAVVDMVTGSHWGILAGLAYYSMVGNWAKVLIAMLLFAGVDGTTHVTGGAQ GRAASSLTSLFSPGPVQHLQLINTNGSWHINRTALSCNDSLNTGFVAALFYKYRFNAS GCPERLATCRPIDTFAQGWGPITYTEPHDLDQRPYCWHYAPQPCGIVPTLQVCGPVYC FTPSPVAVGTTDRFGAPTYRWGANETDVLLLNNAGPPQGNWFGCTWMNGTGFTKTCGG PPCNIGGVGNNTLTCPTDCFRKHPGATYTKCGSGPWLTPRCLVDYPYRLWHYPCTVNF TIFKVRMYVGGAEHRLDAACNWTRGERCDLEDRDRSELSPLLLSTTEWQVLPCSFTTL PALSTGLIHLHQNIVDIQYLYGIGSAVVSFAIKWEYIVLLFLLLADARVCACLWMMLL VAQAEAALENLVVLNAASVAGAHGILSFIVFFCAAWYIKGRLVPGAAYALYGVWPLLL LLLALPPRAYAMDREMAASCGGAVFVGLVLLTLSPHYKVFLARFIWWLQYLITRTEAH LQVWVPPLNVAGGRDAIILLTCVVHPELIFDITKYLLAIFGPLMVLQAGITRVPYFVR AQGLIRACMLARKVVGGHYVQMVFMKLAALAGTYVYDHLTPLRDWAHTGLADLAVAVE PVVFSDMETKVITWGADTAACGDIILALPASARRGKEILLGPADSLEGQGWALLAPIT AYSQQTRGLLGCIITSLTGRDKNQVEGEVQVVSTATQSFLATCINGVCWTVFHGAGSK TLAGPKGPITQMYTNVDQDLVGWPAPPGARSLTPCTCGSSDLYLVTRHADVIPVRARG DGRGSLLPPRPVSYLKGSSGGPLLCPSGHAVGILPAAVCTRGVAMAVEFIPVESMETT MRSPVFTDNPSPPAVPQTFQVAHLHAPTGSGKSTRVPAAYAAQGYKVLVLNPSVAATL GFGAYMSKAHGIDPNLRTGVRTITTGAPITYSTYGKFLADGGGSGGAYDIIMCDECHS TDSTTIYGIGTVLDQAETAGARLVVLSTATPPGSVTVPHLNIEEVALSNTGEIPFYGK AIPIEAIKGGRHLIFCHSKKKCDELAAKLSGLGLNAVAYYRGLDVSVIPTSGDVVVVA TDALMTGFTGDFDSVIDCNTCVTQTVDFSLDPTFTIETTTVPQDAVSRSQRRGRTGRG RAGIYRFVTPGERPSGMFDSSVLCECYDAGCAWYELTPAETSVALRAYLNTPGLPVCQ DHLEFSEGVFTGLTHIDAHFLSQTKQAGENFPYLVAYQATVCARAQAPPPSWDEMWRC LIRLKPTLHGPTPLLYRLGAVQNEVTLTHPITKFIMTCMSADLEVVTSTWVLVGGVLA ALAAYCLTTGSVVIVGRIILSGKPAIIPDREVLYQEFDEMEECASHLPYFEQGMQLAE QFKQKALGLLQTATKQAEAAAPVVESKWRALETFWAKHMWNFISGIQYLAGLSTLPGN PAIRSPMAFTASITSPLTTQHTLLFNILGGWVAAQLAPPSAASAFVGAGIAGAAVGTI GLGKVLVDILAGYGAGVAGALVAFKIMSGEMPSAEDMVNLLPAILSPGALVVGIVCAA ILRRHVGPGEGAVQWMNRLIAFASRGNHVSPRHYVPESEPAARVTQILSSLTITQLLK RLHQWINEDCSTPCSSSWLREIWDWICTVLTDFKTWLQSKLLPRLPGVPFFSCQRGYK GVWRGDGIMHTTCPCGAQITGHVKNGSMRIVGPKTCSNTWYGTFPINAYTTGPCTPSP APNYSKALWRVAAEEYVEVTRVGDFHYVTGMTTDNVKCPCQVPAPEFFTEVDGVALHR YAPACRPLLREEVVFQVGLHQYLVGSQLPCEPEPDVAVLTSMLTDPSHITAETAKRAL ARGSPPSLASSSASQLSAPSLKATCTTHHDSPDADLIEANLLWRQEMGGNITRVESEN KVVILDSFDPLRAEDDEGEISVPAEILRKSRKFPPALPIWAPPDYNPPLLESWKDPDY VPPVVHGCPLPPTKAPPIPPPRRKRTVVLTESTVSSALAELATKTFGSSGSSAIDSGT ATAPPDQASGDGDRESDVESFSSMPPLEGEPGDPDLSDGSWSTVSEEASEDVVCCSMS YTWTGALITPCAAEESKLPINPLSNSLLRHHNMVYATTSRSAGLRQKKVTFDRLQVLD DHYRDVLKEMKAKASTVKAKLLSVEEACKLTPPHSAKSKFGYGAKDVRSLSSRAVTHI RSVWKDLLEDTETPISTTIMAKNEVFCVQPEKGGRKPARLIVFPDLGVRVCEKMALYD VVSTLPQAVMGSSYGFQYSPKQRVEFLVNTWKSKKCPMGFSYDTRCFDSTVTENDIRV EESIYQCCDLAPEAKLAIKSLTERLYIGGPLTNSKGQNCGYRRCRASGVLTTSCGNTL TCYLKATAACRAAKLADCTMLVNGDDLVVICESAGTQEDAASLRVFTEAMTRYSAPPG DPPQPEYDLELITSCSSNVSVAHDASGKRVYYLTRDPTTPLARAAWETARHTPVNSWL GNIIMYAPTLWARMILMTHFFSILLAQEQLEKTLDCQIYGACYSIEPLDLPQIIERLH GLSAFSLHSYSPGEINRVASCLRKLGVPPLRAWRHRARSVRAKLLSQGGRAATCGKYL FNWAVRTKLKLTPIPAASRLDLSGWFVAGYSGGDIYHSLSRARPRWFMLCLLLLSVGV GIYLLPNR SEQ ID NO: 4, nucleocapsid protein of influenza A virus   1 MASQGTKRSY EQMETSGERQ NATEIRASVG RMVGGIGRFY IQMCTELKLS DHEGRLIQNS  61 ITIERMVLSA FDERRNKYLE EHPSAGKDPK KTGGPIYRRR DGKWMRELIL YDKEEIRRIW 121 RQANNGEDAT AGLTHMMIWH SNLNDATYQR TRALVRTGMD PRMCSLMQGS TLPRRSGAAG 181 AAVKGVGTMV MELIRMIKRG INDRNFWRGE NGRRTRIAYE RMCNILKGKF QTAAQRAMMD 241 QVRESRNPGN AEIEDLIFLA RSALILRGSV AHKSCLPACV YGLAVASGYD FEREGYSLVG 301 IDPFRLLQNS QVFSLIRPNE NPAHKSQLVW MACHSAAFED LRVSSFIRGT RVVPRGQLST 361 RGVQIASNEN METMDSSTLE LRSRYWAIRT RSGGNTNQQR ASAGQISVQP TFSVQRNLPF 421 ERATIMAAFT GNTEGRTSDM RTEIIRMMEN ARPEDVSFQG RGVFELSDEK ATNPIVPSFD 481 MSNEGS SEQ ID NO: 5 >gi|73919153|ref|YP_308840.1| matrix protein 2 [Influenza A virus (A/New York/392/2004(H3N2))] MSLLTEVETPIRNEWGCRCNDSSDPLVVAASIIGILHLILWILDRLFFKCVYRLFKHGLKRGPSTEGVPE  70 SMREEYRKEQQNAVDADDSHFVSIELE SEQ ID NO: 6 >gi|73919147|ref|YP_308843.1| nucleocapsid protein [Influenza A virus  (A/New York/392/2004(H3N2))] MASQGTKRSYEQMETDGDRQNATEIRASVGKMIDGIGRFYIQMCTELKLSDHEGRLIQNSLTIEKMVLSA  70 FDERRNKYLEEHPSAGKDPKKTGGPIYARVDGKWMRELVLYDKEEIRRIWRQANNGEDATAGLTHIMIWH 140 SNLNDATYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGIGTMVMELIRMVKAGINDRNFWRGE 210 NGRKTRSAYERMCNILKGKFQTAAQRAMVDQVRESRNPGNAEIEDLIFLARSALILRGSVAHKSCLPACA 280 YGPAVSSGYDFEKEGYSLVGIDPFKLLQNSQIYSLIRPNENPAHKSQLVWMACHSAAFEDLALLSFIRGT 350 KVSPRGKLSTRGVQIASNENMDNMGSSTLELRSGYWAIRTRSGGNTNQQRASAGQTSVQPTFSVQRNLPF 420 EKSTIMAAFTGNTEGRTSDMRAEIIRMMEGAKPEEVSFRGRGVFELSDEKATNPIVPSFDMSNEGSYFFG 490 DNAEEYDN -- SEQ ID NO: 7 >gi|56583270|ref|NP_040979.2| matrix protein 2 [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MSLLTEVETPIRNEWGCRCNGSSDPLAIAANIIGILHLILWILDRLFFKCIYRRFKYGLKGGPSTEGVPK SMREEYRKEQQSAVDADDGHFVSIELE SEQ ID NO: 8 >gi|8486130|ref|NP_040982.1| nucleocapsid protein [Influenza A virus  (A/Puerto Rico/8/34(H1N1))] MASQGTKRSYEQMETDGERQNATEIRASVGKMIGGIGRFYIQMCTELKLSDYEGRLIQNSLTIERMVLSA  FDERRNKYLEEHPSAGKDPKKTGGPIYARVNGKWMRELILYDKEEIRRIWRQANNGDDATAGLTHMMIWH  SNLNDATYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGVGTMVMELVRMIKRGINDRNFWRGE  NGRKTRIAYERMCNILKGKFQTAAQKAMMDQVRESRDPGNAEFEDLTFLARSALILRGSVAHKSCLPACV  YGPAVASGYDFEREGYSLVGIDPFALLQNSQVYSLIRPNENPAHKSQLVWMACHSAAFEDLRVLSFIKGT  KVVPRGKLSTRGVQIASNENMETMESSTLELRSRYWAIRTRSGGNTNQQRASAGQISIQPTFSVQRNLPF  DRTTVMAAFTGNTEGRTSDMRTEIIRMMESARPEDVSFQGRGVFELSDEKAASPIVPSFDMSNEGSYFFG  DNAEEYDN -- SEQ ID NO: 9 >gi|73912687|ref|YP_308853.1| membrane protein M2 [Influenza A virus (A/Korea/426/68(H2N2))] MSLLTEVETPIRNEWGCRCNDSSDPLVVAASIIGILHFILWILDRLFFKCIYRFFKHGLKAGPSTEGVPE SMREEYRKEQQSAVDADDSHFVSIELE SEQ ID NO: 10 >gi|73921307|ref|YP_308871.1| nucleoprotein [Influenza A virus (A/Korea/426/68(H2N2))] MASQGTKRSYEQMETDGERQNATEIRASVGKMIDGIGRFYIQMCTELKLSDYEGRLIQNSLTIERMVLSA FDERRNKYLEEHPSAGKDPKKTGGPIYKRVDGKWMRELVLYDKEEIRRIWRQANNGDDATAGLTHMMIWH SNLNDTTYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGVGTMVMELIRMIKRGINDRNFWRGE NCRKTRSAYERMCNILKCKFQTAAQRAMMDQVRESRNPCNAEIEDLIFLARSALILRGSVAHKSCLPACV YGPAIASGYNFEKEGYSLVGIDPFKLLQNSQVYSLIRPNENPAHKSQLVWMACNSAAFEDLRVLSFIRGT KVSPRGKLSTRGVQIASNENMDTMESSTLELRSRYWAIRTRSGGNTNQQRASAGQISVQPAFSVQRNLPF DKPTIMAAFTGNTEGRTSDMRAEIIRMMEGAKPEEMSFQGRGVFELSDEKATNPIVPSFDMSNEGSYFFG DNAEEYDN SEQ ID NO: 11 >gi|330647|gb|AAA45994.1| pp65 [Human herpesvirus 5] MASVLGPISGHVLKAVFSRGDTPVLPHETRLLQTGIHVRVSQPSLILVSQYTPDSTPCHRGDNQLQVQHT  70 YFTGSEVENVSVNVHNPTGRSICPSQEPMSIYVYALPLKMLNIPSINVHHYPSAAERKHRHLPVADAVIH 140 ASGKQMWQARLTVSGLAWTRQQNQWKEPDVYYTSAFVFPTKDVALRHVVCAHELVCSMENTRATKMQVIG 210 DQYVKVYLESFCEDVPSGKLFMHVTLGSDVEEDLTMTRNPQPFMRPHERNGFTVLCPKNMIIKPGKISHI 280 MLDVAFTSHEHFGLLCPKSIPGLSISGNLLMNGQQIFLEVQAIRETVELRQYDPVAALFFFDIDLLLQRG 350 PQYSEHPTFTSQYRIQGKLEYRHTWDRHDEGAAQGDDDVWTSGSDSDEELVTTERKTPRVTGGGAMAGAS 420 TSAGRKRKSASSATACTAGVMTRGRLKAESTVAPEEDTDEDSDNEIHNPAVFTWPPWQAGILARNLVPMV 490 ATVQGQNLKYQEFFWDANDIYRIFAELEGVWQPAAQPKRRRHRQDALPGPCIASTPKKHRG          541 SEQ ID NO: 12 >gi|33330937|gb|AAQ10712.1| putative transforming protein E6 [Human papillomavirus type 16] MHQKRTAMFQDPQERPGKLPQLCTELQTTIHDIILECVYCKQQLLRREVYDFAFRDLCIVYRDGNPYAVC  70 DKCLKFYSKISEYRHYCYSVYGTTLEQQYNKPLCDLLIRCINCQKPLCPEEKQRHLDKKQRFHNIRGRWT 140 GRCMSCCRSSRTRRETQL SEQ ID NO: 13 >gi|5658327|ref|NP_040979.2| matrix protein 2 [Influenza A virus (A/Puerto Rtco/8/34(HENE))] MSLLTEVETPIRNEWGCRCNGSSDPLAIAANIIGILHLILWILDRLFFKCIYRRFKYGLKGGPSTEGVPK SMREEYRKEQQSAVDADDGHFVSIELE SEQ ID NO: 14 >gi|8486139|ref|NP_040987.1| PB2 protein [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MERIKELRNLMSQSRTREILTKTTVDHMAIIKKYTSGRQEKNPALRMKWMMAMKYPITADKRITEMIPER NEQGQTLWSKMNDAGSDRVMVSPLAVTWWNRNGPMTNTVHYPKIYKTYFERVERLKHGTFGPVHFRNQVK IRRRVDINPGHADLSAKEAQDVIMEVVFPNEVGARILTSESQLTITKEKKEELQDCKISPLMVAYMLERE LVRKTRFLPVAGGTSSVYIEVLHLTQGTCWEQMYTPGGEVKNDDVDQSLIIAARNIVRRAAVSADPLASL LEMCHSTQIGGIRMVDILKQNPTEEQAVGICKAAMGLRISSSFSFGGFTFKRTSGSSVKREEEVLTGNLQ TLKIRVHEGYEEFTMVGRRATAILRKATRRLIQLIVSGRDEQSIAEAIIVAMVFSQEDCMIKAVRGDLNF VNRANQRLNPMHQLLRHFQKDAKVLFQNWGVEPIDNVMGMIGILPDMTPSIEMSMRGVRISKMGVDEYSS TERVVVSIDRFLRVRDQRGNVLLSPEEVSETQGTEKLTITYSSSMMWEINGPESVLVNTYQWIIRNWETV KIQWSQNPTMLYNKMEFEPFQSLVPKAIRGQYSGFVRTLFQQMRDVLGTFDTAQIIKLLPFAAAPPKQSR MQFSSFTVNVRGSGMRILVRGNSPVFNYNKATKRLTVLGKDAGTLTEDPDEGTAGVESAVLRGFLILGKE DRRYGPALSINELSNLAKGEKANVLIGQGDVVLVMKRKRDSSILTDSQTATKRIRMAIN SEQ ID NO: 15 >gi|8486137|ref|NP_040986.1| polymerase PA [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MEDFVRQCFNPMIVELAEKTMKEYGEDLKIETNKFAAICTHLEVCFMYSDFHFINEQGESIIVELGDPNA LLKHRFEIIEGRDRTMAWTVVNSICNTTGAEKPKFLPDLYDYKENRFIEIGVTRREVHIYYLEKANKIKS EKTHIHIFSFTGEEMATKADYTLDEESRARIKTRLFTIRQEMASRGLWDSFRQSERGEETIEERFEITGT MRKLADQSLPPNFSSLENFRAYVDGFEPNGYIEGKLSQMSKEVNARIEPFLKTTPRPLRLPNGPPCSQRS KFLLMDALKLSIEDPSHEGEGIPLYDAIKCMRIFFGWKEPNVVKPHEKGINPNYLLSWKQVLAELQDIEN EEKIPKTKNMKKISQLKWALGENMAPEKVDFDDCKDVGDLKQYDSDEPELRSLASWIQNEFNKACELTDS SWIELDEIGEDVAPIEHIASMRRNYFTSEVSHCRATEYIMKGVYINTALLNASCAAMDDFQLIPMISKCR TKEGRRKINLYGFIIKGRSHLRNDTDVVNFVSMEFSLTDPRLEPHKWEKYCVLEIGDMLLRSAIGQVSRP MFLYVRINGTSKIKMKWGMEMRRCLLQSLQQIESMIEAESSVKEKDMIKEFFENKSETWPIGESPKGVEE SSIGKVCRILLAKSVFNSLYASPQLEGFSAESRKLLLIVQALRDNLEPGIFDLGGLYEAIEECLINDPWV LLNASWFNSFLTHALS SEQ ID NO: 16 >gi|8486133|ref|NP_040984.1| nonstructural protein NS1 [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MDPNTVSSFQVDCFLWHVRKRVADQELGDAPFLDRLRRDQKSLRGRGSTLGLDIETATRAGKQIVERILK EESDEALKMTMASVPASRYLTDMTLEEMSREWSMLIPKQKVAGPLCIRMDQAIMDKNIILKANFSVIFDR LETLILLRAFTEEGAIVGEISPLPSLPGHTAEDVKNAVGVLIGGLEWNDNTVRVSETLQRFAWRSSNENG RPPLTPKQKREMAGTIRSEV SEQ ID NO: 17 >gi|8486132|ref|NP_040983.1| nonstructural protein NS2 [Influenza A virus (A/Puerto Rico/8/34(H1N1)) MDPNTVSSFQDILLRMSKMQLESSSEDLNGMITQFESLKLYRDSLGEAVMRMGDLHSLQNRNEKWREQLG QKFEEIRWLIEEVRHKLKVTENSFEQITFMQALHLLLEVEQEIRTFSFQLI SEQ ID NO: 18 >gi|8486128|ref|NP_040981.1| neuraminidase [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MNPNQKIITIGSICLVVGLISLILQIGNIISIWISHSIQTGSQNHTGICNQNIITYKNSTWVKDTTSVIL TGNSSLCPIRGWAIYSKDNSIRIGSKGDVFVIREPFISCSHLECRTFFLTQGALLNDRHSNGTVKDRSPY RALMSCPVGEAPSPYNSRFESVAWSASACHDGMGWLTIGISGPDNGAVAVLKYNGIITETIKSWRKKILR TQESECACVNGSCFTIMTDGPSDGLASYKIFKIEKGKVTKSIELNAPNSHYEECSCYPDTGKVMCVCRDN WHGSNRPWVSFDQNLDYQIGYICSGVFGDNPRPKDGTGSCGPVYVDGANGVKGFSYRYGNGVWIGRTKSH SSRHGFEMIWDPNGWTETDSKFSVRQDVVAMTDWSGYSGSFVQHPELTGLDCIRPCFWVELIRGRPKEKT IWTSASSISFCGVNSDTVDWSWPDGAELPFTIDK SEQ ID NO: 19 >gi|8486126|ref|NP_040980.1| haemagglutinin [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MKANLLVLLCALAAADADTICIGYHANNSTDTVDTVLEKNVTVTHSVNLLEDSHNGKLCRLKGIAPLQLG KCNIAGWLLGNPECDPLLPVRSWSYIVETPNSENGICYPGDFIDYEELREQLSSVSSFERFEIFPKESSW PNHNTTKGVTAACSHAGKSSFYRNLLWLTEKEGSYPKLKNSYVNKKGKEVLVLWGIHHPSNSKDQQNIYQ NENAYVSVVTSNYNRRFTPEIAERPKVRDQAGRMNYYWTLLKPGDTIIFEANGNLIAPRYAFALSRGFGS GIITSNASMHECNTKCQTPLGAINSSLPFQNIHPVTIGECPKYVRSAKLRMVTGLRNIPSIQSRGLFGAI AGFIEGGWTGMIDGWYGYHHQNEQGSGYAADQKSTQNAINGITNKVNSVIEKMNIQFTAVGKEFNKLEKR MENLNKKVDDGFLDIWTYNAELLVLLENERTLDFHDSNVKNLYEKVKSQLKNNAKEIGNGCFEFYHKCDN ECMESVRNGTYDYPKYSEESKLNREKVDGVKLESMGIYQILAIYSTVASSLVLLVSLGAISFWMCSNGSL QCRICI SEQ ID NO: 20 >gi|8486123|ref|NP_040978.1| matrix protein 1 [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MSLLTEVETYVLSIIPSGPLKAEIAQRLEDVFAGKNTDLEVLMEWLKTRPILSPLTKGILGFVFTLTVPS ERGLQRRRFVQNALNGNGDPNNMDKAVKLYRKLKREITFHGAKEISLSYSAGALASCMGLIYNRMGAVTT EVAFGLVCATCEQIADSQHRSHRQMVTTTNPLIRHENRMVLASTTAKAMEQMAGSSEQAAEAMEVASQAR QMVQAMRTIGTHPSSSAGLKNDLLENLQAYQKRMGVQMQRFK SEQ ID NO: 21 >gi|83031685|ref|YP_418248.1| PB1-F2 protein [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MGQEQDTPWILSTGHISTQKRQDGQQTPKLEHRNSTRLMGHCQKTMNQVVMPKQIVYWKQWLSLRNPILV FLKTRVLKRWRLFSKHE SEQ ID NO: 22 >gi|8486135|ref|NP_040985.1| polymerase 1 PB1 [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MDVNPTLLFLKVPAQNAISTTFPYTGDPPYSHGTGTGYTMDTVNRTHQYSEKARWTTNTETGAPQLNPID GPLPEDNEPSGYAQTDCVLEAMAFLEESHPGIFENSCIETMEVVQQTRVDKLTQGRQTYDWTLNRNQPAA TALANTIEVFRSNGLTANESGRLIDFLKDVMESMKKEEMGITTHFQRKRRVRDNMTKKMITQRTIGKRKQ RLNKRSYLIRALTLNTMTKDAERGKLKRRAIATPGMQIRGFVYFVETLARSICEKLEQSGLPVGGNEKKA KLANVVRKMMTNSQDTELSLTITGDNTKWNENQNPRMFLAMITYMTRNQPEWFRNVLSIAPIMFSNKMAR LGKGYMFESKSMKLRTQIPAEMLASIDLKYFNDSTRKKIEKIRPLLIEGTASLSPGMMMGMFNMLSTVLG VSILNLGQKRYTKTTYWWDGLQSSDDFALIVNAPNHEGIQAGVDRFYRTCKLHGINMSKKKSYINRTGTF EFTSFFYRYGFVANFSMELPSFGVSGSNESADMSIGVTVIKNNMINNDLGPATAQMALQLFIKDYRYTYR CHRGDTQIQTRRSFEIKKLWEQTRSKAGLLVSDGGPNLYNIRNLHIPEVCLKWELMDEDYQGRLCNPLNP FVSHKEIESMNNAVMMPAHGPAKNMEYDAVATTHSWIPKRNRSILNTSQRGVLEDEQMYQRCCNLFEKFF PSSSYRRPVGISSMVEAMVSRARIDARIDFESGRIKKEEFTEIMKICSTIEELRRQK SEQ ID NO: 23 >gi|8486130|ref|NP_040982.1| nucleocapsid protein [Influenza A virus (A/Puerto Rico/8/34(H1N1))] MASQGTKRSYEQMETDGERQNATEIRASVGKMIGGIGRFYIQMCTELKLSDYEGRLIQNSLTIERMVLSA FDERRNKYLEEHPSAGKDPKKTGGPIYRRVNGKWMRELILYDKEEIRRIWRQANNGDDATAGLTHMMIWH SNLNDATYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGVGTMVMELVRMIKRGINDRNFWRGE NGRKTRIAYERMCNILKGKFQTAAQKAMMDQVRESRDPGNAEFEDLTFLARSALILRGSVAHKSCLPACV YGPAVASGYDFEREGYSLVGIDPFRLLQNSQVYSLIRPNENPAHKSQLVWMACHSAAFEDLRVLSFIKGT KVVPRGKLSTRGVQIASNENMETMESSTLELRSRYWAIRTRSGGNTNQQRASAGQISIQPTFSVQRNLPF DRTTVMAAFTGNTEGRTSDMRTEIIRMMESARPEDVSFQGRGVFELSDEKAASPIVPSFDMSNEGSYFFG DNAEEYDN SEQ ID NO: 24 >gi|F73918826|ref|YP_308855.1| polymerase 2 [Influenza A virus (A/Korea/426/1968(H2N2))] MERIKELRNLMSQSRTREILTKTTVDHMAIIKKYTSGRQEKNPSLRMKWMMAMKYPITADKRITEMVPER NEQGQTLWSKMSDAGSDRVMVSPLAVTWWNRNGPMTSTVHYPKIYKTYFEKVERLKHGTFGPVHFRNQVK IRRRVDINPGHADLSAKEAQDVIMEVVFPNEVGARILTSESQLTITKEKKEELQDCKISPLMVAYMLERE LVRKTRFLPVAGGTSSVYIEVLHLTQGTCWEQMYTPGGEVRNDDVDQSLIIAARNIVRRAAVSADPLASL LEMCHSTQIGGTRMVDILRQNPTEEQAVDICKAAMGLRISSSFSFGGFTFKRTSGSSIKREEEVLTGNLQ TLKIRVHEGYEEFTMVGKRATAILRKATRRLVQLIVSGRDEQSIAEAIIVAMVFSQEDCMIKAVRGDLNF VNRANQRLNPMHQLLRHFQKDAKVLFQNWGIEHIDNVMGMIGVLPDMTPSTEMSMRGIRVSKMGVDEYSS TERVVVSIDRFLRVRDQRGNVLLSPEEVSETQGTEKLTITYSSSMMWEINGPESVLVNTYQWIIRNWETV KIQWSQNPTMLYNKMEFEPFQSLVPKAIRGQYSGFVRTLFQQMRDVLGTFDTTQIIKLLPFAAAPPKQSR MQFSSLTVNVRGSGMRILVRGNSPVFNYNKTTKRLTILGKDAGTLTEDPDEGTSGVESAVLRGFLILGKE DRRYGPALSINELSTLAKGEKANVLIGQGDVVLVMKRKRDSSILTDSQTATKRIRMAIN SEQ ID NO: 25 >gi|73919145|ref|YP_308850.1| hemagglutinin [Influenza A virus (A/Korea/426/68(H2N2))] MAIIYLILLFTAVRGDQICIGYHANNSTEKVDTILERNVTVTHAKDILEKTHNGKLCKLNGIPPLELGDC SIAGWLLGNPECDRLLSVPEWSYIMEKENPRYSLCYPGSFNDYEELKHLLSSVKHFEKVKILPKDRWTQH TTTGGSWACAVSGKPSFFRNMVWLTRKGSNYPVAKGSYNNTSGEQMLIIWGVHHPNDEAEQRALYQNVGT YVSVATSTLYKRSIPEIAARPKVNGLGRRMEFSWTLLDMWDTINFESTGNLVAPEYGFKISKRGSSGIMK TEGTLENCETKCQTPLGAINTTLPFHNVHPLTIGECPKYVKSEKLVLATGLRNVPQIESRGLFGAIAGFI EGGWQGMVDGWYGYHHSNDQGSGYAADKESTQKAFNGITNKVNSVIEKMNTQFEAVGKEFSNLEKRLENL NKKMEDGFLDVWTYNAELLVLMENERTLDFHDSNVKNLYDKVRMQLRDNVKELGNGCFEFYHKCDNECMD SVKNGTYDYPKYEEESKLNRNEIKGVKLSSMGVYQILAIYATVAGSLSLAIMMAGISFWMCSNGSLQCRI CI SEQ ID NO: 26 >gi|73912688|ref|YP_308854.1| membrane protein M1 [Influenza A virus (A/Korea/426/68(H2N2))] MSLLTEVETYVLSIVPSGPLKAEIAQRLEDVFAGKNTDLEALMEWLKTRPILSPLTKGILGFVFTLTVPS ERGLQRRRFVQNALNGNGDPNNMDRAVKLYRKLKREITFHGAKEVALSYSAGALASCMGLIYNRMGAVIT EVAFAVVCATCEQIADSQHRSHRQMVITTNPLIRHENRMVLASTTAKAMEQMAGSSEQAAEAMEVASQAR QMVQAMRAIGTPPSSSAGLKDDLLENLQAYQKRMGVQMQRFK SEQ ID NO: 27 >gi|73912687|ref|YP_308853.1| membrane protein M2 [Influenza A virus (A/Korea/426/68(H2N2))] MSLLTEVETPIRNEWGCRCNDSSDPLVVAASIIGILHFILWILDRLFFKCIYRFFKHGLKRGPSTEGVPE SMREEYRKEQQSAVDADDSHFVSIELE SEQ ID NO: 28 >gi|73912685|ref|YP_308852.1| polymerase PA [Influenza A virus (A/Korea/426/68(H2N2))] MEDFVRQCFNPMIVELAEKAMKEYGEDLKIETNKFAAICTHLEVCFMYSDFHFINEQGESIMVELDDPNA LLKHRFEIIEGRDRTMAWTVVNSICNTTGAEKPKFLPDLYDYKENRFIEIGVTRREVHIYYLEKANKIKS ENTHIHIFSFTGEEMATKADYTLDEESRARIKTRLFTIRQEMANRGLWDSFRQSERGEETIEERFEITGT MRRLADQSLPPNFSCLENFRAYVDGFEPNGYIEGKLSQMSKEVNAKIEPFLKTTPRPIRLPDGPPCFQRS KFLLMDALKLSIEDPSHEGEGIPLYDAIKCMRTFFGWKEPYIVKPHEKGINPNYLLSWKQVLAELQDIEN EEKIPRTKNMKKTSQLKWALGENMAPEKVDFDNCRDISDLKQYDSDEPELRSLSSWIQNEFNKACELTDS IWIELDEIGEDVAPIEHIASMRRNYFTAEVSHCRATEYIMKGVYINTALLNASCAAMDDFQLIPMISKCR TKEGRRKTNLYGFIIKGRSHLRNDTDVVNFVSMEFSLTDPRLEPHKWEKYCVLEIGDMLLRSAIGQMSRP MFLYVRTNGTSKIKMKWGMEMRPCLLQSLQQIESMVEAESSVKEKDMTKEFFENKSETWPIGESPKGVEE GSIGKVCRTLLAKSVFNSLYASPQLEGFSAESRKLLLVVQALRDNLEPGTFDLGGLYEAIEECLINDPWV LLNASWFNSFLTHALR SEQ ID NO: 29 >gi|73921833|ref|YP_308877.1| PB1-F2 protein [Influenza A virus (A/Korea/426/68(H2N2))] MGQEQDTPWTQSTEHINIQKRGSGQQTRKLERPNLTQLMDHYLRTMNQVDMHKQTASWKQWLSLRNHTQE SLKIRVLKRWKLFNKQEWTN SEQ ID NO: 30 >gi|73912683|ref|YP_308851.1| PB1 polymerase subunit [Influenza A virus (A/Korea/426/68(H2N2))] MDVNPTLLFLKVPAQNAISTTFPYTGDPPYSHGTGTGYTMDTVNRTHQYSEKGKWTTNTETGAPQLNPID GPLPEDNEPSGYAQTDCVLEAMAFLEESHPGIFENSCLETMEVIQQTRVDKLTQGRQTYDWTLNRNQPAA TALANTIEVFRSNGLTANESGRLIDFLKDVIESMDKEEMEITTHFQRKRRVRDNMTKKMVTQRTIGKKKQ RLNKRSYLIRALTLNTMTKDAERGKLKRRAIATPGMQIRGFVHFVETLARNICEKLEQSGLPVGGNEKKA KLANVVRKMMTNSQDTELSFTITGDNTKWNENQNPRVFLAMITYITRNQPEWFRNVLSIAPIMFSNKMAR LGKGYMFESKSMKLRTQIPAEMLASIDLKYFNESTRKKIEKIRPLLIDGTVSLSPGMMMGMFNMLSTVLG VSILNLGQKKYTKTTYWWDGLQSSDDFALIVNAPNHEGIQAGVNRFYRTCKLVGINMSKKKSYINRTGTF EFTSFFYRYGFVANFSMELPSFGVSGINESADMSIGVTVIKNNMINNDLGPATAQMALQLFIKDYRYTYR CHRGDTQIQTRRSFELKKLWEQTRSKAGLLVSDGGSNLYNIRNLHIPEVCLKWELMDEDYQGRLCNPLNP FVSHKEIESVNNAVVMPAHGPAKSMEYDAVATTHSWTPKRNRSILNTSQRGILEDEQMYQKCCNLFEKFF PSSSYRRPVGISSMVEAMVSRARIDARIDFESGRIKKEEFAEIMKICSTIEELRRQK SEQ ID NO: 31 >gi|73921567|ref|YP_308869.1| non-structural protein N52 [Influenza A virus (A/Korea/426/68(H2N2))] MDSNTVSSFQDILLRMSKMQLGSSSEDLNGMITQFESLKLYRDSLGEAVMRMGDLHSLQNRNGKWREQLG QKFEEIRWLIEEVRHRLKITENSFEQITFMQALQLLFEVEQEIRTFSFQLI SEQ ID NO: 32 >gi|73921566|ref|YP_308870.1| non-structural protein NS1 [Influenza A virus (A/Korea/426/68(H2N2))] MDSNTVSSFQVDCFLWHVRKQVVDQELGDAPFLDRLRRDQKSLRGRGSTLDLDIEAATRVGKQIVERILK EESDEALKMTMASAPASRYLTDMTIEELSRDWFMLMPKQKVEGPLCIRIDQAIMDKNIMLKANFSVIFDR LETLILLRAFTEEGAIVGEISPLPSLPGHTIEDVKNAIGVLIGGLEWNDNTVRVSKTLQRFAWRSSNENG RPPLTPKQKRKMARTIRSKVRRDKMAD SEQ ID NO: 33 >gi|73921307|ref|YP_308871.1| nucleoprotein [Influenza A virus (A/Korea/426/68(H2N2))] MASQGTKRSYEQMETDGERQNATEIRASVGKMIDGIGRFYIQMCTELKLSDYEGRLIQNSLTIERMVLSA FDERRNKYLEEHPSAGKDPKKTGGPIYKRVDGKWMRELVLYDKEEIRRIWRQANNGDDATAGLTHMMIWH SNLNDTTYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGVGTMVMELIRMIKRGINDRNFWRGE NGRKTRSAYERMCNILKGKFQTAAQRAMMDQVRESRNPGNAEIEDLIFLARSALILRGSVAHKSCLPACV YGPAIASGYNFEKEGYSLVGIDPFKLLQNSQVYSLIRPNENPAHKSQLVWMACNSAAFEDLRVLSFIRGT KVSPRGKLSTRGVQIASNENMDTMESSTLELRSRYWAIRTRSGGNTNQQRASAGQISVQPAFSVQRNLPF DKPTIMAAFTGNTEGRTSDMRAEIIRMMEGAKPEEMSFQGRGVFELSDEKATNPIVPSFDMSNEGSYFFG DNAEEYDN SEQ ID NO: 34 >gi|73921304|ref|YP_308872.1| neuraminidase [Influenza A virus (A/Korea/426/68(H2N2))] MNPNQKIITIGSVSLTIATVCFLMQIAILVTTVTLHFKQHECDSPASNQVMPCEPIIIERNITEIVYLNN TTIEKEICPEVVEYRNWSKPQCQITGFAPFSKDNSIRLSAGGDIWVTREPYVSCDPGKCYQFALGQGTTL DNKHSNDTIHDRIPHRTLLMNELGVPFHLGTRQVCVAWSSSSCHDGKAWLHVCVTGDDKNATASFIYDGR LMDSIGSWSQNILRTQESECVCINGTCTVVMTDGSASGRADTRILFIEEGKIVHISPLSGSAQHVEECSC YPRYPDVRCICRDNWKGSNRPVIDINMEDYSIDSSYVCSGLVGDTPRNDDRSSNSNCRNPNNERGNPGVK GWAFDNGDDVWMGRTISKDLRSGYETFKVIGGWSTPNSKSQINRQVIVDSNNWSGYSGIFSVEGKRCINR CFYVELIRGRQQETRVWWTSNSIVVFCGTSGTYGTGSWPDGANINFMPI SEQ ID NO: 35 >gi|73919213|ref|YP_308844.1| nonstructural protein 2 [Influenza A virus (A/New York/392/2004(H3N2))] MDSNTVSSFQDILLRMSKMQLGSSSEDLNGMITQFESLKIYRDSLGEAVMRMGDLHLLQNRNGKWREQLG QKFEEIRWLIEEVRHRLKTTENSFEQITFMQALQLLFEVEQEIRTFSFQLI SEQ ID NO: 36 >gi|73919212|ref|YP_308845.1| nonstructural protein 1 [Influenza A virus (A/New York/392/2004(H3N2))] MDSNTVSSFQVDCFLWHIRKQVVDQELSDAPFLDRLRRDQRSLRGRGNTLGLDIKAATHVGKQIVEKILK EESDEALKMTMVSTPASRYITDMTIEELSRNWFMLMPKQKVEGPLCIRMDQAIMEKNIMLKANFSVIFDR LETIVLLRAFTEEGAIVGEISPLPSFPGHTIEDVKNAIGVLIGGLEWNDNTVRVSKNLQRFAWRSSNENG GPPLTPKQKRKMARTARSKV SEQ ID NO: 37 >gi|73919207|ref|YP_308839.1| hemagglutinin [Influenza A virus (A/New York/392/2004(H3N2))] MKTIIALSYILCLVFAQKLPGNDNSTATLCLGHHAVPNGTIVKTITNDQIEVTNATELVQSSSTGGICDS PHQILDGENCTLIDALLGDPQCDGFQNKKWDLFVERSKAYSNCYPYDVPDYASLRSLVASSGTLEFNNES FNWTGVTQNGTSSACKRRSNNSFFSRLNWLTHLKFKYPALNVTMPNNEKFDKLYIWGVHHPGTDNDQISL YAQASGRITVSTKRSQQTVIPSIGSRPRIRDVPSRISIYWTIVKPGDILLINSTGNLIAPRGYFKIRSGK SSIMRSDAPIGKCNSECITPNGSIPNDKPFQNVNRITYGACPRYVKQNTLKLATGMRNVPEKQTRGIFGA IAGFIENGWEGMVDGWYGFRHQNSEGTGQAADLKSTQAAINQINGKLNRLIGKTNEKFHQIEKEFSEVEG RIQDLEKYVEDTKIDLWSYNAELLVALENQHTIDLTDSEMNKLFERTKKQLRENAEDMGNGCFKIYHKCD NACIGSIRNGTYDHDVYRDEALNNRFQIKGVELKSGYKDWILWISFAISCFLLCVALLGFIMWACQKGNI RCNICI SEQ ID NO: 38 >gi|73919153|ref|YP_308840.1| matrix protein 2 [Influenza A virus (A/New York/392/2004(H3N2))] MSLLTEVETPIRNEWGCRCNDSSDPLVVAASIIGILHLILWILDRLFFKCVYRLFKHGLKRGPSTEGVPE SMREEYRKEQQNAVDADDSHFVSIELE SEQ ID NO: 39 >gi|73919152|ref|YP_308841.1| matrix protein 1 [Influenza A virus (A/New York/392/2004(H3N2))] MSLLTEVETYVLSIVPSGPLKAEIAQRLEDVFAGKNTDLEALMEWLKTRPILSPLTKGILGFVFTLTVPS ERGLQRRRFVQNALNGNGDPNNMDKAVKLYRKLKREITFHGAKEIALSYSAGALASCMGLIYNRMGAVTT EVAFGLVCATCEQIADSQHRSHRQMVATTNPLIKHENRMVLASTTAKAMEQMAGSSEQAAEAMEIASQAR QMVQAMRAVGTHPSSSTGLRDDLLENLQTYQKRMGVQMQRFK SEQ ID NO: 40 >gi|73919150|ref|YP_308848.1| PB1-F2 protein [Influenza A virus (A/New York/392/2004(H3N2))] MEQEQDTPWTQSTEHTNIQRRGSGRQIQKLGHPNSTQLMDHYLRIMSQVDMHKQTVSWRLWPSLKNPTQV SLRTHALKQWKSFNKQGWTN SEQ ID NO: 41 >gi|73919149|ref|YP_308847.1| polymerase PB1 [Influenza A virus (A/New York/392/2004(H3N2))] MDVNPTLLFLKVPAQNAISTTFPYTGDPPYSHGTGTGYTMDTVNRTHQYSEKGKWTTNTETGAPQLNPID GPLPEDNEPSGYAQTDCVLEAMAFLEESHPGIFENSCLETMEVVQQTRVDKLTQGRQTYDWTLNRNQPAA TALANTIEVFRSNGLTANESGRLIDFLKDVMESMDKEEMEITTHFQRKRRVRDNMTKKMVTQRTIGKKKQ RVNKRGYLIRALTLNTMTKDAERGKLKRRAIATPGMQIRGFVYFVETLARSICEKLEQSGLPVGGNEKKA KLANVVRKMMTNSQDTELSFTITGDNTKWNENQNPRMFLAMITYITKNQPEWFRNILSIAPIMFSNKMAR LGKGYMFESKRMKLRTQIPAEMLASIDLKYFNESTRKKIEKIRPLLIDGTASLSPGMMMGMFNMLSTVLG VSVLNLGQKKYTKTTYWWDGLQSSDDFALIVNAPNHEGIQAGVDRFYRTCKLVGINMSKKKSYINKTGTF EFTSFFYRYGFVANFSMELPSFGVSGINESADMSIGVTVIKNNMINNDLGPATAQMALQLFIKDYRYTYR CHRGDTQIQTRRSFELKKLWDQTQSRAGLLVSDGGPNLYNIRNLHIPEVCLKWELMDENYRGRLCNPLNP FVSHKEIESVNNAVVMPAHGPAKSMEYDAVATTHSWNPKRNRSILNTSQRGILEDEQMYQKCCNLFEKFF PSSSYRRPIGISSMVEAMVSRARIDARIDFESGRIKKEEFSEIMKICSTIEELRRQK SEQ ID NO: 42 >gi|F73919147|ref|YP_308843.1| nucleocapsid protein [Influenza A virus (A/New York/392/2004(H3N2))] MASQGTKRSYEQMETDGDRQNATEIRASVGKMIDGIGRFYIQMCTELKLSDHEGRLIQNSLTIEKMVLSA FDERRNKYLEEHPSAGKDPKKTGGPIYRRVDGKWMRELVLYDKEEIRRIWRQANNGEDATAGLTHIMIWH SNLNDATYQRTRALVRTGMDPRMCSLMQGSTLPRRSGAAGAAVKGIGTMVMELIRMVKRGINDRNFWRGE NGRKTRSAYERMCNILKGKFQTAAQRAMVDQVRESRNPGNAEIEDLIFLARSALILRGSVAHKSCLPACA YGPAVSSGYDFEKEGYSLVGIDPFKLLQNSQIYSLIRPNENPAHKSQLVWMACHSAAFEDLRLLSFIRGT KVSPRGKLSTRGVQIASNENMDNMGSSTLELRSGYWAIRTRSGGNTNQQRASAGQTSVQPTFSVQRNLPF EKSTIMAAFTGNTEGRTSDMRAEIIRMMEGAKPEEVSFRGRGVFELSDEKATNPIVPSFDMSNEGSYFFG DNAEEYDN SEQ ID NO: 43 >gi|73919136|ref|YP_308842.1| neuraminidase [Influenza A virus (A/New York/392/2004(H3N2))] MNPNQKIITIGSVSLTISTICFFMQIAILITTVTLHFKQYEFNSPPNNQVMLCEPTIIERNITEIVYLTN TTIEKEMCPKLAEYRNWSKPQCDITGFAPFSKDNSIRLSAGGDIWVTREPYVSCDPDKCYQFALGQGTTL NNVHSNDTVHDRTPYRTLLMNELGVPFHLGTKQVCIAWSSSSCHDGKAWLHVCVTGDDKNATASFIYNGR LVDSIVSWSKKILRTQESECVCINGTCTVVMTDGSASGKADTKILFIEEGKIIHTSTLSGSAQHVEECSC YPRYPGVRCVCRDNWKGSNRPIVDINIKDYSIVSSYVCSGLVGDTPRKNDSSSSSHCLDPNNEEGGHGVK GWAFDDGNDVWMGRTISEKLRSGYETFKVIEGWSKPNSKLQINRQVIVDRGNRSGYSGIFSVEGKSCINR CFYVELIRGRKEETEVLWTSNSIVVFCGTSGTYGTGSWPDGADINLMPI SEQ ID NO: 44 >gi|73919134|ref|YP_308846.1| polymerase PA [Influenza A virus (A/New York/392/2004(H3N2))] MEDFVRQCFNPMIVELAEKAMKEYGEDLKIETNKFAAICTHLEVCFMYSDFHFINEQGESIVVELDDPNA LLKHRFEIIEGRDRTMAWTVVNSICNTTGAEKPKFLPDLYDYKENRFIEIGVTRREVHIYYLEKANKIKS ENTHIHIFSFTGEEIATKADYTLDEESRARIKTRLFTIRQEMANRGLWDSFRQSERGEETIEEKFEISGT MRRLADQSLPPKFSCLENFRAYVDGFEPNGCIEGKLSQMSKEVNAKIEPFLKTTPRPIKLPNGPPCYQRS KFLLMDALKLSIEDPSHEGEGIPLYDAIKCIKTFFGWKEPYIVKPHEKGINSNYLLSWKQVLSELQDIEN EEKIPRTKNMKKTSQLKWALGENMAPEKVDFDNCRDISDLKQYDSDEPELRSLSSWIQNEFNKACELTDS IWIELDEIGEDVAPIEYIASMRRNYFTAEVSHCRATEYIMKGVYINTALLNASCAAMDDFQLIPMISKCR TKEGRRKTNLYGFIIKGRSHLRNDTDVVNFVSMEFSLTDPRLEPHKWEKYCVLEIGDMLLRSAIGQISRP MFLYVRTNGTSKVKMKWGMEMRRCLLQSLQQIESMIEAESSIKEKDMTKEFFENKSEAWPIGESPKGVEE GSIGKVCRTLLAKSVFNSLYASPQLEGFSAESRKLLLVVQALRDNLEPGTFDLGGLYEAIEECLINDPWV LLNASWFNSFLTHALK SEQ ID NO: 45 >gi|13919060|ref|YP_308849.1| polymerase PB2 [Influenza A virus (A/New York/392/2004(H3N2))] MERIKELRNLMSQSRTREILTKTTVDHMAIIKKYTSGRQEKNPSLRMKWMMAMKYPITADKRITEMVPER NEQGQTLWSKMSDAGSDRVMVSPLAVTWWNRNGPVASTVHYPKVYKTYFDKVERLKHGTFGPVHFRNQVK IRRRVDINPGHADLSAKEAQDVIMEVVFPNEVGARILTSESQLTITKEKKEELRDCKISPLMVAYMLERE LVRKTRFLPVAGGTSSIYIEVLHLTQGTCWEQMYTPGGEVRNDDVDQSLIIAARNIVRRAAVSADPLASL LEMCHSTQIGGTRMVDILRQNPTEEQAVDICKAAMGLRISSSFSFGGFTFKRTSGSSVKKEEEVLTGNLQ TLKIRVHEGYEEFTMVGKRATAILRKATRRLVQLIVSGRDEQSIAEAIIVAMVFSQEDCMIKAVRGDLNF VNRANQRLNPMHQLLRHFQKDAKVLFQNWGIEHIDSVMGMVGVLPDMTPSTEMSMRGIRVSKMGVDEYSS TERVVVSIDRFLRVRDQRGNVLLSPEEVSETQGTERLTITYSSSMMWEINGPESVLVNTYQWIIRNWEAV KIQWSQNPAMLYNKMEFEPFQSLVPKAIRSQYSGFVRTLFQQMRDVLGTFDTTQIIKLLPFAAAPPKQSR MQFSSLTVNVRGSGMRILVRGNSPVFNYNKTTKRLTILGKDAGTLIEDPDESTSGVESAVLRGFLIIGKE DRRYGPALSINELSNLAKGEKANVLIGQGDVVLVMKRKRDSSILTDSQTATKRIRMAIN SEQ ID NO: 46: CMV Protein IE122: >gi|39841910|gb|AAR31478.1| UL122 [Human herpesvirus 5] MESSAKRKMDPDNPDEGPSSKVPRPETPVTKATTFLQTMLRKEVNSQLSLGDPLFPELAEESLKTFEQVT EDCNENPEKDVLAELGDILAQAVNHAGIDSSSTGHTLTTHSCSVSSAPLNKPTPTSVAVTNTPLPGASAT PELSPRKKPRKTTRPFKVIIKPPVPPAPIMLPLIKQEDIKPEPDFTIQYANKIIDTAGCIVISDSEEEQG EEVETRGATASSPSTGSGTPRVTSPTHPLSQMNHPPLPDPLARPDEDSSSSSSSSCSSASDSESESEEMK CSSGGGASVTSSHHGRGGFGSAASSSLLSCGHQSSGGASTGPRKKKSKRISELDNEKVANIMKDKNTPFCTPNVQTRAG RVKIDEVSRMFRNTNRSLEYKNLPFTIPSMHQVLDEAIKACKTMQVNNKGIQIIYTRNHEVKSEVDAVRCRLGTMCNLA LSTPFLMEHTMPVTHPPEVAQRTADACNEGVKAAWSLKELHTHQLCPRSSDYRNMIIHAATPVDLLGALNLCLPLMQKF PKQVMVRIFSTNQGGFMLPIYETAAKAYAVGQFEQPTETPPEDLDTLSLATEAAIQDLANKSQ SEQ ID NO: 126: >gi|4927721|gb|AAD33253.1|AF125673_2 E7 [Human papillomavirus type 16] MHGDTPTLHEYMLDLQPETTDLYCYEQLNDSSEEEDEIDGPAGQAEPDRAHYNIVTFCCKCDSTLRLCVQ STHVDIRTLEDLLMGTLGIVCPICSQKP

Example 1

The peptides according to the invention used in the following examples were synthesized by Schafer-N as c-terminal amides using the Fmoc-strategy of Sheppard, (1978) J. Chem. Soc., Chem. Commun., 539.

Cell Penetration Assay

A set of peptides were biotinylated on N-terminal, and different combinations of aminoacids, with respect to length and type, were added to the sequence box X1, X3 and X4 in the peptides as illustrated by the diagram below. The peptides were tested on cells grown from one individual blood donor.

Schematic diagram of amino acid sequence of the peptides according to the invention (Each X defines a sequence of amino acids):

X1 X2 X3 X4 X5

SP_2 to SP_17 are variants of 51n_Biotin, from a specific native domain on the HCV core protein.

Intracellular Staining for Biotinylated Peptides

96-well U-bottom polystyrene plates (NUNC, cat no: 163320) were used for staining of human PBMCs. Briefly, 8 ul of N- or C-terminally biotinylated peptides according to table 1 or table 2 (i.e. 5 mM, 2.5 mM & 1.25 mM tested for each peptide) were incubated at 37° C. for 2 h with 40 ul of PBMC (12.5×106 cells/ml) from blood donors. Cells were then washed 3× with 150 ul of Cellwash (BD, cat no: 349524), followed by resuspension of each cell pellet with 100 ul of Trypsin-EDTA (Sigma, cat no: T4424), then incubated at 37° C. for 5 min. Trypsinated cells were then washed 3× with 150 ul of Cellwash (BD, cat no: 349524), followed by resuspension with BD Cytofix/Cytoperm™ plus (BD, cat no: 554715), then incubated at 4° C. for 20 min according to manufacturer. Cells were then washed 2× with 150 ul PermWash (BD, cat no: 554715). Cells were then stained with Streptavidin-APC (BD, cat no: 554067) & Anti-hCD11c (eBioscience, cat no: 12-0116) according to manufacturer at 4° C. for 30 min aiming to visualize biotinylated peptides & dendritic cells, respectively. Cells were then washed 3× with 150 ul PermWash, followed by resuspension in staining buffer (BD, cat no: 554656) before flow cytometry. Dendritic cells were gated as CD11c+ events outside lymphocyte region (i.e. higher FSC & SSC signals than lymphocytes). 200 000 total cells were acquired on a FACSCanto II flow cytometer with HTS loader, and histograms for both total cells & dendritic cells with respect to peptide-fluorescence (i.e. GeoMean) were prepared.

Extracellular Staining for Biotinylated Peptides

96-well U-bottom polystyrene plates (NUNC, cat no: 163320) were used for staining of human PBMCs. Briefly, 8 ul of N- or C-terminally biotinylated peptides according to table 1 or table 2 (i.e. 5 mM, 2.5 mM & 1.25 mM tested for each peptide; all peptides manufactured by Schafer) were incubated at 37° C. for 2 h with 40 ul of PBMC (12.5×106 cells/ml) from blood donors. Cells were then washed 3× with 150 ul of Cellwash (BD, cat no: 349524), then stained with Streptavidin-APC (BD, cat no: 554067) & Anti-hCD11c (eBioscience, cat no: 12-0116) according to manufacturer at 4° C. for 30 min aiming to visualize biotinylated peptides & dendritic cells, respectively. Cells were then washed 3× with 150 ul of Cellwash (BD, cat no: 349524), followed by resuspension in staining buffer (BD, cat no: 554656) before flow cytometry. Dendritic cells were gated as CD11c+ events outside lymphocyte region (i.e. higher FSC & SSC signals than lymphocytes). 200 000 total cells were acquired on a FACSCanto II flow cytometer with HTS loader, and histograms for both total cells & dendritic cells with respect to peptide-fluorescence (i.e. GeoMean) were prepared.

It was clearly seen that the arginine added on the beginning, middle and in the end improves the ability to enter the cell. It was observed that the variations of arginine decides the ability to enter the cell, best result are achieved with two in the beginning and two in the middle—but variations of different amount of arginines all show good result.

The data shown in the tables below are geomean-value of each testet peptide, as calculated by the FACS Duva software. The Geomean values by trypsinating/Cytofix/Cytoperm:

TABLE 3 With Cytofix/Cytoperm and trypsination Concentration BC20 833 μM 417 μM 208 μM 104 μM 51n_Biotin ND ND ND ND SP 2 3136 5486 1211 SP 3 40456 25905 10788 4308 Sp 4 41491 28008 7540 2946 Sp 5 40534 46060 19065 6152 Sp 6 32577 22195 6514 1850 Sp 7 47922 30503 10481 2766 SP 8 31976 28606 9617 2917 SP 9 11344 6060 2945 1268 SP 10 43389 18607 7684 3709 SP 11 8262 3562 1277 601 SP 12 11089 10869 8679 4316 SP 13 568 394 332 SP 14 1059 682 392 62 SP 15 1810 477 848 600 SP 16 4558 2240 1260 505 SP 17 30248 29967 12244 1500 SP 18 4869 1334 1971 1038 SP 19 17018 7201 3466 1625 SP 20 7319 2457 1268 445 −ve 0 0 0 0 +ve 18694 26046 15340 7182 No 224 106 78 168 peptide

As shown in table 4 the peptides according to the invention had the ability to allocate through the cell membrane.

TABLE 4 Results on DC-cells with low concentration of peptides (208 uM). The results are sorted in descending order (with respect to BC 16). Peptide BC 16 BC43 no pept 4473 2488 NO pept 4003 2359 NO pept 7799 P-biotin 22058 33545 P-biotin 5568 26212 P-biotin 28169 n-biotin 3745 1967 N-biotin 3591 3631 N-biotin 2271 SP61_2 128330 150491 42 74920 65811 SP42_1 73973 SP17 67428 SP51_1* 66582 BI10026 65196 43536 SP11b_1 64047 42b 61968 19181 SP22 61597 18624 51 biotin 59789 33935 SP12 59274 31222 BI100260 47846 SP61_3 47182 36803 V10 45430 120b 44185 100-22b 43537 28780 BI100260b 37702 SP12_c 37100 43386 18b 29740 33597 SP13 28539 9129 BI10024b 26892 13002 SP21 26525 4294 61b biotin 25611 24416 SP61b_2 25489 310-11-n- 25236 sc 100-12 24792 45622 SP5 21358 29146 SP4_c 20673 30786 SP7_c 20041 11832 SP20 19051 3383 190n 18616 23383 SP3_c 18505 26308 SP24 18181 63639 SP6_c 17964 38487 SP42b_1 17628 SP23 17084 12801 SP5_c 16908 24403 SP7 16064 21414 SP8 15379 17836 BI-050sc5 13648 15549 190 12906 SP61_4 12829 190b 12391 20444 SP17_c 11830 SP25 11552 SP4 10751 17372 SP6 10233 14468 SP3 9480 10573 SP1_c 9234 SP8_c 9159 23763 SP10 8627 9216 19 8417 6372 SP9 8356 10084 N13 7982 5953 51b 7000 6082 SP10_c 6904 SP2 6677 6112 310-11 6537 SP19 6522 6536 SP11 6490 13230 SP9_c 6180 7758 BI-050sc1 6056 6160 BI-050sc2 6019 11584 SP16 5730 3656 51n 5551 7721 SP18 5545 7751 310-11n 5436 SP11_c 5371 7878 SP15 5076 2539 N10 4597 SP14 3704 1629 SP2_c 323 13341 SP13_c 60307 42n

Example 2

Positive CTL Response May Alternatively be Assayed by ELISPOT Assay.

Human IFN-Gamma Cytotoxic T-Cell (CTL) Response by ELISPOT Assay

Briefly, at day 1, PBMC samples from HCV patients were incubated in flasks (430 000 PBMCs/cm2) for 2 h at 37° C., 5% CO2 in covering amount of culture media (RPMI 1640 Fisher Scientific; Cat No. PAAE15-039 supplemented with L-Glutamine, (MedProbe Cat. No. 13E17-605E, 10% Foetal Bovine serum (FBS), Fisher Scientific Cat. No. A15-101) and Penicillin/Streptomycin, (Fisher Acientific Cat. No. P11-010) in order to allow adherence of monocytes. Non-adherent cells were isolated, washed, and frozen in 10% V/V DMSO in FBS until further usage. Adherent cells were carefully washed with culture media, followed by incubation at 37° C. until day 3 in culture media containing 2 μg/ml final concentration of hrGM-CSF (Xiamen amoytop biotech co, cat no: 3004.9090.90) & 1 μg/ml hrIL-4 (Invitrogen, Cat no: PHC0043), and this procedure was then repeated at day 6. At day 7, cultured dendritic cells (5 000-10 000 per well) were added to ELISPOT (Millipore multiscreen HTS) plates coated with 0.5 μg/well anti-human y Interferon together with thawed autologous non-adherent cells (200 000 per well), antigen samples (1-8 ug/ml final concentration for peptide antigens; 5 ug/ml final concentration for Concanavalin A (Sigma, Cat no: C7275) or PHA (Sigma, Cat no: L2769)) & anti-Anergy antibodies (0.03-0.05 ug/ml final concentration for both anti-PD-1 (eBioscience, cat no: 16-9989-82) & anti-PD-L1 (eBioscience, cat no: 16-5983-82)). Plates were incubated overnight and spots were developed according to manufacturer. Spots were read on ELISPOT reader (CTL-ImmunoSpot® S5 UV Analyzer).

TABLE 5  ELISPOT of core proteins Patient A Patient B Patient C Patient D ConA 5090 5035 2605 2725 1355 700 529 512 No Pep 20 25 10 25 10 0 4 I Irr. peptide 10 30 40 5 45 0 1 2 RRSRNLGKVIDTLTC 310-42b 90 115 60 80 70 25 13 11 BRLMGYIPLVGA RRIRNLGRVIETLTG 310-42  75 80 95 30 25 55 13 11 BRLZGYIPLIGA RRGYIPLVGAPLGBR 310-51b 45 40 50 85 45 75 9 13 VARALAHGVRV RRGYLPAVGAPIGBR 310-51  40 75 50 60 100 35 9 9 VIRVIAHGLRL RRNYATGNLPGRRGC 310-61b 45 35 25 45 55 40 15 17 SFSIFLLAL RRGGGQIIGGNYLIP 310-11  ND ND ND ND ND ND 11 14 RBGPBIGVRATB

Table 5—Results from IFN-g ELISPOT run on scaffold peptides with domains derived from HCV proteins

The peptides had in general a higher amount of T-cell spots compared to No Peptide and the irrelevant control peptide. This clearly indicates that the peptides have a positive immunological effect in HCV-patients.

Example 3

The REVEAL & ProVE® Rapid Epitope Discovery System in Detail

Binding properties to HLA for the ninemers listed in table 6 were tested for the following HLA-classes:

HLA-A1, HLA-A2, HLA-A3, HLA-A11, HLA-A24, HLA-A29, HLA-B7, HLA-B8, HLA-B14, HLA-B15, HLA-B27, HLA-B35, HLA-B40.

The peptides were synthesized as a Prospector PEPscreen®: Custom Peptide Library. Peptides 8-15 amino acids in length were synthesized in 0.5-2 mg quantities with high average purity. Quality control by MALDI-TOF Mass Spectrometry was carried out on 100% of samples.

The REVEAL′″ binding assay determined the ability of each candidate peptide to bind to one or more MHC class I alleles and stabilizing the MHC-peptide complex. By comparing the binding to that of high and intermediate affinity T cell epitopes, the most likely immunogenic peptides in a protein sequence can be identified. Detection is based on the presence or absence of the native conformation of the MHC-peptide complex.

Each peptide is given a score relative to the positive control peptide, which is a known T cell epitope. The score of the test peptide is reported quantitatively as a percentage of the signal generated by the positive control peptide, and the peptide is indicated as having a putative pass or fail result. Assay performance is confirmed by including an intermediate control peptide that is known to bind with weaker affinity to the allele under investigation.

TABLE 6 AA HLA-type place- A1 A2 A3 A11 A24 A29 B7 B8 B14 B15 B27 B35 B40 ment Positive Control in HCV- 100.00 100.00 100.0 100.00 100.00 100.00 100.00 100.00 100.00 100.00 100.00 100.0 100.00 core Linear Intermediate Control protein Sequence 8.41 8.79 10 14.95 10 30.52 12.00 56.60 24.21 56.88 10.49 93.56 76.48 163-171 NYATGNLPG 11.16 3.94 8.65 4.69 1.13 34.26 0.51 9.96 0.79 6.06 2.33 6.44 75.28 ″ NYVTGNIPG N/D N/D N/D N/D N/D N/D N/D N/D N/D N/D N/D N/D N/D (mod) 164-172 YATGNLPGC 8.10 22.46 3.67 2.16 1.20 18.82 0.76 9.51 0.41 5.09 2.44 4.52 77.49 ″ YVTGNIPGS 13.33 6.88 5.34 5.18 2.71 10.29 2.70 12.40 0.76 6.16 1.98 4.42 88.29 (mod) 165-173 ATGNLPGCS 7.13 4.62 3.64 2.54 0.64 22.84 1.12 10.73 0.87 3.81 2.56 7.00 90.48 ″ VTGNIPGST 16.18 8.44 2.52 4.85 1.60 15.05 2.24 13.12 0.75 5.15 1.58 4.00 103.97 (mod) 166-174 TGNLPGCSF 11.97 5.18 3.71 2.56 4.81 18.89 2.38 8.62 0.86 45.07 2.37 11.40 73.71 ″ TGNIPGSTY 10.58 3.59 13.04 6.06 0.86 35.10 1.32 10.25 1.15 52.30 1.98 48.40 38.51 (mod) 167-175 GNLPGCSFS 6.44 6.11 3.54 2.41 1.13 13.48 1.84 8.71 0.81 3.96 13.44 4.80 80.68 ″ GNIPGSTYS 7.54 5.07 5.04 1.54 0.00 24.38 0.94 6.32 0.34 4.80 1.58 7.86 55.59 (mod) 168-176 NLPGCSFSI 13.15 47.28 8.15 3.47 85.91 22.34 1.54 9.89 0.36 3.11 3.37 5.31 60.68 ″ NIPGSTYSL 8.41 5.71 3.98 3.20 8.50 31.99 4.80 7.66 0.46 4.46 2.29 4.71 37.01 (mod) 171-179 GCSFSIFLL 3.65 5.69 1.85 4.77 2.18 8.96 2.88 11.10 0.32 4.28 2.53 3.03 52.58 ″ GITFSIYLI 9.61 7.27 1.42 4.88 3.05 10.42 2.07 8.94 0.63 8.15 3.29 9.27 68.30 (mod) 172-180 CSFSIFLLA 9.69 23.38 5.68 9.00 1.37 6.45 2.22 9.85 0.93 11.66 2.99 4.96 33.53 ″ ITFSIYLIV 9.89 43.08 1.66 5.31 0.77 24.10 4.32 11.38 1.53 6.68 4.79 12.30 78.84 (mod) 173-181 SFSIFLLAL 5.68 2.70 1.42 2.21 3.28 30.35 1.44 7.98 0.60 8.89 3.06 5.33 21.04 ″ TFSIYLIVS 9.93 2.02 0.91 2.89 0.60 8.58 1.28 9.52 0.37 8.63 1.49 2.48 23.23 (mod) 174-182 SRNLGKVID 15.30 4.94 3.46 4.45 0.71 9.94 1.28 16.71 0.67 11.25 1.28 4.59 33.93 ″ IRNLGRVIE 14.22 8.77 3.89 5.31 0.61 11.06 1.43 9.10 30.77 4.06 1.84 1.98 21.40 (mod) 175-183 RNLGKVIDT 18.90 6.42 3.15 6.22 1.04 10.18 2.42 13.80 0.61 11.79 2.73 4.40 48.14 ″ RNLGRVIET 15.93 5.96 5.52 13.68 0.51 15.13 0.71 15.51 0.26 8.84 0.91 2.34 27.57 (mod) 176-184 NLGKVIDTL 18.14 7.70 6.41 12.81 1.16 10.67 2.64 16.86 0.57 12.59 2.64 4.39 53.82 ″ NLGRVIETL 18.24 11.97 2.86 4.53 0.86 16.44 1.47 15.58 0.07 16.29 1.66 2.82 38.91 (mod) 177-185 LGKVIDTLT 22.08 4.05 7.39 12.95 0.70 15.99 0.94 17.96 0.43 7.14 2.90 5.11 44.92 ″ LGRVIETLT 16.33 5.90 7.40 20.27 0.97 12.31 2.66 14.74 0.28 16.38 2.54 3.43 62.07 (mod) 178-186 GKVIDTLTC 14.77 4.89 3.69 3.96 0.41 14.26 0.25 13.63 0.16 7.31 0.84 3.11 19.45 ″ GRVIETLTS 14.42 5.26 12.46 27.62 0.88 15.59 1.25 12.91 0.20 8.31 1.05 3.56 38.91 (mod) 179-187 KVIDTLTCG 15.77 19.13 4.27 8.91 0.57 13.16 0.57 13.17 0.18 10.13 0.63 2.74 32.89 ″ RVIETLTSG 11.61 9.82 2.23 3.25 0.96 15.52 0.50 11.83 0.11 37.99 2.32 1.90 32.30 (mod) 180-188 VIDTLTCGF 25.85 5.14 2.93 6.00 0.95 13.90 0.45 10.00 0.11 9.49 1.11 3.26 27.24 ″ VIETLTSGF 14.61 4.84 2.55 3.66 0.82 13.07 0.71 12.96 0.35 10.37 1.38 2.39 24.04 (mod) 131-139 ADLMGYIPL 31.05 8.06 1.93 3.35 0.61 14.51 0.73 11.40 0.13 8.30 1.01 2.08 26.33 ″ AEL[Nle]G 16.63 7.49 3.05 3.61 0.37 20.78 1.11 14.74 0.12 10.20 0.77 1.91 72.73 (mod) YIPL 132-140 DLMGYIPLV 16.67 103.34 4.66 5.01 1.14 25.64 4.84 22.65 0.23 7.67 1.05 2.49 39.33 ″ EL[Nle]GY 18.29 97.87 4.54 3.21 0.92 20.93 0.68 17.05 0.14 8.91 0.67 2.55 43.10 (mod) IPLI 133-141 LMGYIPLVG 14.17 31.94 2.53 2.13 0.51 24.26 0.41 20.75 0.08 9.43 1.44 0.81 33.55 ″ L[Nle]GYI 14.33 49.48 3.98 2.48 0.71 25.94 0.89 17.29 0.15 14.60 0.73 2.85 57.46 (mod) PLIG 134-142 MGYIPLVGA 11.34 10.71 3.40 4.79 0.35 19.54 0.80 14.88 0.73 8.85 0.83 0.85 40.78 ″ [Nle]GYIP 17.87 10.43 3.13 7.27 1.33 27.85 1.78 21.35 0.29 11.07 1.42 5.89 60.84 (mod) LIGA 135-143 GYIPLVGAP 15.62 7.28 3.46 3.84 0.80 29.74 1.37 15.94 0.47 11.02 1.76 10.35 72.32 ″ GYLPAVGAP 12.04 5.87 2.90 4.25 0.35 26.03 3.10 17.38 0.11 10.50 0.73 1.84 27.82 (mod) 136-144 YIPLVGAPL 21.80 35.00 5.29 3.54 4.51 31.09 41.87 33.10 0.13 54.57 0.69 99.81 30.22 ″ YLPAVGAPI 15.76 75.80 2.58 3.07 4.65 28.40 7.70 17.92 0.12 49.63 0.51 2.03 64.34 (mod) 137-145 IPLVGAPLG 13.28 4.32 2.59 2.05 0.60 26.79 2.34 17.87 0.03 10.01 0.35 30.74 41.10 ″ LPAVGAPIG 20.57 5.60 3.02 4.95 0.61 25.32 8.12 15.87 0.12 10.10 0.49 1.06 39.31 (mod) 147-155 VARALAHGV 16.10 5.85 2.77 3.47 0.32 29.43 31.59 14.31 0.17 11.26 0.62 0.27 44.29 ″ VIRVIAHGL 18.66 8.60 4.29 4.54 0.28 27.12 29.93 32.81 0.55 9.64 1.16 2.51 52.64 (mod) 148-156 ARALAHGVR 20.62 6.72 2.35 3.83 1.15 31.96 4.70 18.91 1.10 13.58 3.55 2.45 50.23 ″ IRVIAHGLR 15.82 4.83 3.58 2.50 0.50 23.19 3.50 13.34 0.10 8.99 9.37 0.66 26.45 (mod) 149-157 RALAHGVRV 20.77 8.69 2.51 4.45 0.84 29.73 2.55 18.08 0.46 11.84 6.37 6.07 70.26 ″ RVIAHGLRL 11.60 18.68 13.32 17.75 0.79 23.22 102.96 12.60 0.42 106.77 15.57 1.43 24.08 (mod) 27-35 GGQIVGGVY 13.97 6.88 3.47 2.71 1.78 20.46 3.99 14.66 0.32 110.34 0.66 0.54 30.75 ″ GGQIIGGNY 24.04 7.06 2.23 2.40 0.39 14.38 1.09 10.52 0.25 90.62 0.24 2.22 15.03 (mod) 28-36 GQIVGGVYL 15.07 55.85 4.80 4.46 0.50 13.73 6.56 14.53 0.37 182.45 1.01 3.24 24.20 ″ GQIIGGNYL 20.65 12.96 3.01 2.77 0.47 14.17 2.39 11.90 0.22 173.66 0.64 2.60 31.55 (mod) 29-37 QIVGGVYLL 20.25 57.04 2.36 1.96 1.01 13.36 28.66 13.15 0.37 15.07 0.60 4.01 24.51 ″ QIIGGNYLI 21.63 73.54 6.30 4.06 12.60 13.60 52.04 10.61 0.40 29.59 0.91 8.99 83.60 (mod) 30-38 IVGGVYLLP 22.11 6.78 1.88 3.10 0.30 12.38 24.16 11.48 1.65 15.00 0.68 2.68 19.83 ″ IIGGNYLIP 21.14 8.27 3.88 2.81 10.95 13.88 15.47 12.18 1.17 19.93 0.97 5.35 65.43 (mod) 31-39 VGGVYLLPR 17.88 8.73 3.41 4.16 0.34 14.20 1.15 11.57 0.44 13.22 0.79 4.02 55.61 ″ IGGNYLIPR 17.90 7.04 2.88 3.57 0.89 14.85 20.49 14.23 0.32 15.02 0.82 2.54 25.44 (mod) 41-49 GPRLGVRAT 13.85 6.23 2.45 1.60 0.05 12.66 124.37 13.18 0.94 10.01 0.68 1.83 19.95 ″ GP[Cit]IG 18.60 9.16 3.48 2.72 0.16 11.88 5.38 9.99 0.13 7.29 0.59 2.25 19.61 (mod) VRAT 42-50 PRLGVRATR 17.77 6.85 3.63 2.73 0.97 13.35 42.64 11.46 0.14 10.04 0.86 1.65 14.52 ″ P[Cit]IGV 18.83 7.36 2.52 1.72 0.21 14.14 1.91 9.47 0.19 12.64 0.94 2.45 49.29 (mod) RAT[Cit] 43-51 RLGVRATRK 20.39 6.71 112.23 102.85 0'28 12.83 1.67 10.21 0.07 11.74 33.13 2.83 23.05 ″ [Cit]IGVR 19.68 8.17 25.16 8.27 0.50 16.67 14.59 12.09 0.17 14.45 0.86 8.51 18.45 (mod) AT[Cit]R

Example 4

Intracellular Staining:

Peptides according to the invention with X2 and X4 derived from HCV, Influenza, or CMV were prepared and tested for intracellular staining in an experiment as described above in the “Cell penetration assay”.

Peptide X4 (Different from X2 no. Antigen X1 X2 X3 unless indicated) X5 median n 1 Negative control PVVHLTLRQAGDDFSR 1.00 37 2 Neg control in  RRG PVVHLTL RRRG QAGDDFS 4.12 18 scaffold 3 Positive control RQIKIWFQNRRMKWKK 2.73 8 4 Positive control  YGRKKRRQRRR 4.43 24 (tat) 5 HCV (Native  11 amino acids G 11 amino acids 1.84 18 sequence) 6 HCV R 11 amino acids of native seq 11 amino acids of native seq R 5.35 24 7 HCV R 11 amino acids  RRR 11 amino acids  R 11.59 4 (1 substitution) (5 substitution) 8 HCV RR 11 amino acids of native seq RR 11 amino acids of native seq 6.92 27 9 HCV RR 11 amino acids of native seq RRR 11 amino acids of native seq 3.25 21 10 HCV (Not scaffold) EE 11 amino acids of native seq EE 11 amino acids of native seq L16 26 11 HCV (Not scaffold) GG 11 amino acids of native seq GG 11 amino acids of native seq 2.01 28 12 HCV (Native  23 amino acids 3.01 12 sequence) 13 HCV RR 13 amino acids RR 10 amino acids of native seq 21.43 8 14 HCV RR 13 amino acids RR 10 amino acids 4.81 21 15 HCV (Not scaffold) EE 13 amino acids EE  9 amino acids 1.16 19 16 Influenza (Native 23 amino acids 3.70 3 sequence) 17 Flu BR 10 amino acids BRGR  8 amino acids 20.77 3 18 cmv R  9 amino acids BRR =X2 B 3.86 3 19 HCV W 11 amino acids of native seq RR 11 amino acids of native seq 17.41 13 20 HCV RR 22 amino acids RR 22 amino acids R 13.25 5

Extracellular Staining for the Same Peptides 1-15:

Peptide no. Antigen median n 1 Negative control 1.00 35 2 Neg control in scaffold 1.77 20 3 Positive control 9.15 19 5 HCV Native sequence 2.08 21 6 HCV 2.20 29 7 HCV 29.42 12 8 HCV 3.06 28 9 HCV 2.06 23 10 HCV (Not scaffold) 1.95 27 11 HCV (Not scaffold) 2.62 23 12 HCV (Native sequence) 1.76 14 13 HCV 16.80 7 14 HCV 17.00 16 15 HCV (Not scaffold) 2.38 12 19 HCV 1.37 19 20 HCV 126.5 7

Results: It was seen that peptides on scaffold form, compared to native peptides or peptides with other amino acids in X1, X3 and X5 had improved uptake.

Claims

1. An isolated nucleic acid or polynucleotide encoding a cell-penetrating peptide comprising the following structure wherein X1 and X3 independently defines a linear sequence of any 1, 2, 3 or 4 amino acids independently selected from any basic amino acid, citrulline, tryptophan, or a derivative thereof; X2 defines a linear sequence of 8-30 amino acids derived from an antigen; X4 defines a linear sequence of 8-30 amino acids derived from said antigen, said sequence X4 being different from X2; and wherein X5 is any one optional amino acid selected from a basic amino acid, citrulline, tryptophan, or a derivative thereof.

X1-X2-X3-X4-X5  (formula I),

2. The isolated nucleic acid or polynucleotide according to claim 1, wherein said basic amino acid is independently selected from Arg, Lys, and His.

3. The isolated nucleic acid or polynucleotide according to claim 1, wherein the peptide comprises one or more cysteine.

4. The isolated nucleic acid or polynucleotide according to claim 1, wherein the N- and/or C-terminal amino acid in X2 is a hydrophilic or polar amino acid.

5. The isolated nucleic acid or polynucleotide according to claim 1, wherein the N-terminal amino acid in X4 is a hydrophilic or polar amino acid.

6. The isolated nucleic acid or polynucleotide according to claim 1, wherein X1 and/or X3 consist of 2 or 3 amino acids

7. The isolated nucleic acid or polynucleotide according to claim 6, wherein X1 consists of WW, BR, or RR.

8. The isolated nucleic acid or polynucleotide according to claim 6, wherein X3 consists of WW, BR, or RR.

9. The isolated nucleic acid or polynucleotide according to claim 1, wherein X2 and/or X4 is not derived from HIV.

10. The isolated nucleic acid or polynucleotide according to claim 1, wherein X2 and/or X4 is a linear sequence of less than 12 amino acids.

11. The isolated nucleic acid or polynucleotide according to claim 1, wherein X2 and/or X4 is derived from HCV, CMV, HPV, Influenza, adenoviruses, or picornaviruses.

12. A vector comprising the nucleic acid or polynucleotide according to claim 1.

13. A host cell comprising the vector according to claim 12.

14. An immunogenic composition comprising the nucleic acid or polynucleotide according to claim 1, in combination with a pharmaceutically acceptable diluent or vehicle and optionally an immunological adjuvant.

15. The immunogenic composition according to claim 14 in the form of a vaccine composition.

16. A method for inducing an immune response in a subject against an antigen which comprises administration of the nucleic acid or polynucleotide according to claim 1.

17. A method for inducing an immune response in a subject against an antigen which comprises administration of the vector according to claim 12.

18. A method for reducing and/or delaying the pathological effects of a virus in a subject infected with said virus, the method comprising administering an effective amount of the nucleic acid or polynucleotide according to claim 1.

19. A method for reducing and/or delaying the pathological effects of a virus in a subject infected with said virus, the method comprising administering an effective amount of the vector according to claim 12.

Patent History
Publication number: 20170112917
Type: Application
Filed: Dec 21, 2016
Publication Date: Apr 27, 2017
Applicant: Bionor Immuno AS (Skien)
Inventors: Einar Tønnes Lange (Skien), Maja Sommerfelt Grønvold (Risør), Jens Olof Holmberg (Helsingborg), Birger Sørensen (Skien)
Application Number: 15/386,963
Classifications
International Classification: A61K 39/245 (20060101); C12N 7/00 (20060101); A61K 39/145 (20060101); C07K 14/005 (20060101); A61K 39/29 (20060101);