H. Pylori Lipopolysaccharide Outer Core Epitope
Helicobacter pylori, one of the most common human pathogens, is associated with the development of human chronic gastritis, peptic ulcers and gastric cancer. The invention relates to a α1,6-glucan-containing Helicobacter pylori compound comprising the structure of Formula I: wherein R is a α-DDHep-3-α-L-Fuc-3-β-GlcNAc trisaccharide substituted with an α1,6-glucan linked to an α1,3-DD-heptan, and wherein the last DD-Hep residue of α1,3-DD-heptan is capped with β-GlcNAc residue. Compositions comprising the compound, uses of the compound, and antibodies raised against the compound are also described.
The instant application is a divisional application of U.S. patent application Ser. No. 14/739,013, filed Jun. 15, 2015, which is a divisional application of U.S. patent application Ser. No. 13/321,881, filed Mar. 2, 2012, now U.S. Pat. No. 9,085,610, which is a 371 of PCT Application CA10/01173, filed Jul. 30, 2010, now abandoned, which claims the benefit of US Provisional Patent Application, filed Apr. 29, 2009 No. 61/230,315, entitled ‘H. PYLORI LIPOPOLYSACCHARIDE OUTER CORE EPITOPE’, now abandoned, the contents of which are incorporated herein by reference.
FIELD OF INVENTIONThe present invention relates to a novel Helicobacter pylori LPS outer core epitope. More specifically, the present invention relates to a novel H. pylori outer core epitope, its synthesis, characterization, and conjugation.
BACKGROUND OF THE INVENTIONHelicobacter pylori is recognized as the most common bacterial infection associated with human chronic gastritis, peptic ulcer and gastric carcinoma. H. pylori infection has an estimated prevalence of about half the world's population, reaching up to 70% in developing countries and 20-30% in industrialized countries (Dunn et al., 1997). The vast majority of individuals acquire H. pylori in childhood; the prevalence of infection among children in developing countries is linked to a low socio-economic status and poor sanitation (Castillo-Rojas et al., 2004). H. pylori has been identified by the World Health Organization (WHO) as a class I carcinogen, as it increases the relative risk for gastric cancer at least six-fold. Gastric cancer is the second most common cause of mortality worldwide, and accounts for 700,000 annual deaths (Parkin et al., 2002).
Current eradication strategies of H. pylori are based on the use of proton pump inhibitors and antibiotics. However, the efficacy of chemotherapeutic intervention is limited by frequency of antibiotic resistance among H. pylori isolates and lack of immunity against re-infection. Thus, novel therapies are needed to provide a global strategy for the prevention and eradication of H. pylori infections.
While recent investigations have been focused on the role of protein components in the pathogenesis of H. pylori and their role in protective immunity (Ruggiero et al., 2003; Rossi et al., 2004), relatively few studies have explored the possibility of including antigens other than proteins in vaccine formulations (Angelakopoulos and Hohmann, 2000). For example, polysaccharide-based conjugate vaccines are known to prevent systemic infection and inhibit colonization of the host (Anderson et al., 1986; Chu et al., 1991; Pon et al., 1997; Passwell et al., 2001; Passwell et al., 2003). Recent studies of enteric pathogens have examined approaches based on LPS conjugates as candidate vaccines for human use (Gu et al., 1996; Mieszala et al., 2003; Cox et al., 2005; Yu and Gu, 2007).
Lipopolysaccharide (LPS) is a major cell surface component of H. pylori. Structural studies carried out on a number of H. pylori isolates (Monteiro, 2001) have resulted in a structural model of LPS consisting of an O-chain and a core oligosaccharide that is attached to a lipid A moiety. The structure of the 0-chain polysaccharide backbone of most H. pylori strains is unique and displays type 2 and/or type 1 Lewis (Le) blood group determinants that mimic those present on the cell surface of human gastric and tumour cells (Wirth et al., 1996); these may be implicated in adverse autoimmune reactions leading to atrophic gastritis (Appelmelk et al., 1996). In addition, the outer core region of H. pylori LPS contains two unusual polymeric components: DD-heptoglycan and α1,6-glucan (Monteiro, 2001). The α1,6-glucan polymer in the outer core region H. pylori LPS isolates is synthesized by the product of the HP0159 open reading frame. The presence and expression of HP0159 gene in H. pylori is common.
A number of H. pylori LPS biosynthetic genes have been characterized and their role in pathogenesis and colonization determined (Logan et al., 2000; Logan et al., 2005; Hiratsuka et al., 2005; Chandan et al., 2007; Altman et al., 2008). H. pylori HP0826 mutants were constructed and it was demonstrated that this mutation resulted in formation of truncated LPS lacking Le antigen (Logan et al., 2000). However, full characterization of the structure of the LPS was not achieved.
Despite advances in the field, immunogenic epitopes effective across multiple types of H. pylori remain elusive.
SUMMARY OF THE INVENTIONThe present invention relates to a novel Helicobacter pylori LPS outer core epitope. More specifically, the present invention relates to a novel H. pylori outer core epitope, its synthesis, characterization, and conjugation.
The present invention provides a α1,6-glucan-containing Helicobacter pylori compound comprising the structure of Formula I:
R is a α-DDHep-3-α-L-Fuc-3-β-GlcNAc trisaccharide substituted with an α1,6-glucan linked to an α1,3-DD-heptan, and the last DD-Hep residue of α1,3-DD-heptan is capped with β-GlcNAc residue. In the compound as just described, the α1,6-glucan may comprise from about 3 to about 12 α1,6-linked glucose residues, and the α1,3-DD-heptan may comprise from about 2 to about 6 α1,3-linked heptose residues.
The R group of the compound as described above may be
where β-GlcNAc residue L is linked to O-2 of Hep G. In the compound as just described, residues Q and Z of the glucan are α1,6-linked glucose residues, and n may be any value between about 1 to 11; residues T, Y, and X are α1,3-linked heptose residues, and m may be any value between about 0 to 4.
The compound as described above may be isolated or purified from H. pylori strain HP0826::Kan.
In the compounds described above, the structure of Formula I may further comprise a lipid A moiety covalently attached to the Kdo residue C. The lipid A molecule may be O-deacylated or may be cleaved through hydrolysis of the ketosidic linkage of the Kdo residue.
The present invention also provides a conjugate, comprising a substantially linear α1,6-glucan-containing compound conjugated to a linker molecule, a protein carrier, or a combination thereof. The substantially linear α1,6-glucan-containing compound may be the compound described herein, wherein the structure of Formula I is conjugated to the linker molecule, protein carrier, or combination thereof. The substantially linear α1,6-glucan-containing compound may alternatively be a Dextran, such as Dextran T5. The protein carrier may be tetanus toxoid or bovine serum albumin.
The present invention also encompasses a composition comprising one or more than one compounds or conjugates as described above.
The present invention further includes an antibody directed against the α1,6-glucan epitope-containing compound described herein. The antibody may be monoclonal antibody 1C4F9. The invention further encompasses hybridoma cell line 1C4F9, which produces monoclonal antibody 1C4F9.
The monoclonal antibody described above may be utilized to cause complement-mediated bacteriolysis of α1,6-glucan-expressing H. pylori strains in an individual in need of such treatment.
The present invention also provides the use of an effective amount of the composition described above for inducing an immune response against H. pylori in an individual. The compound(s) in the composition may be conjugated to a suitable carrier protein; additionally, the compound(s) in the composition may be conjugated to a suitable carrier protein via a 2-keto-3-deoxy-octulosonic acid (Kdo) of the lipopolysaccharide.
The present invention further provides an immune antiserum produced by immunizing a mammal with the immunogenic composition described herein. The immune antiserum may comprise an IgG recognizing an α1,6-linked glucan epitope in homologous and heterologous typeable and non-typeable mutant and wild-type strains of H. pylori. The IgG may cause complement-mediated bacteriolysis of mutant and wild-type α1,6-glucan-expressing H. pylori strains.
Additional aspects and advantages of the present invention will be apparent in view of the following description. The detailed description and examples, while indicating preferred embodiments of the invention, are given by way of illustration only, as various changes and modifications within the scope of the invention will become apparent to those skilled in the art in light of the teachings of this invention.
These and other features of the invention will now be described by way of example, with reference to the appended drawings, wherein:
The present invention relates to a novel Helicobacter pylori LPS outer core epitope. More specifically, the present invention relates to a novel H. pylori outer core epitope, its synthesis, characterization, and conjugation.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned hereunder are incorporated herein by reference.
As used herein, ‘purified’ does not necessarily mean absolute purity but rather is intended as a relative definition. Similarly, as used herein, ‘isolated’ refers to the removal of something from its native environment.
Helicobacter pylori is a bacterial pathogen commonly associated with human chronic gastritis, peptic ulcer and gastric carcinoma; as a result of the increased risk of gastric cancer associated with H. pylori infection, it has been classified as a class I carcinogen. Lipopolysaccharide (LPS) is a major cell surface component of H. pylori. Prior publications relating to structural studies of H. pylori LPS led to a proposed model where an O-chain polysaccharide is covalently linked to a core oligosaccharide, which is in turn attached to a lipid A moiety. The O-chain polysaccharide backbone of most H. pylori strains is unique and can display type 2 and/or type 1 Lewis (Le) blood group determinants; this polysaccharide component is antigenic. “Typeable” H. pylori strains have Lewis epitopes (Le X and/or Le Y antigens) that can be recognized by anti-Lewis antibodies (anti-Le); such antibodies may be commercially available and assist in typing. “Non-typeable” strains do not contain Lewis structures.
Further structural studies established that the outer core region of H. pylori LPS contains two unusual polymeric components: DD-heptoglycan and α1,6-glucan side chains (Monteiro, 2001). Logan et al. (2000) also provided insight regarding the structure of the LPS. Specifically, the proposed structures (see
The present invention provides a novel α1,6-glucan-containing Helicobacter pylori compound comprising the structure of Formula I:
wherein R is a α-DDHep-3-α-L-Fuc-3-β-GlcNAc trisaccharide substituted with an α1,6-glucan followed by α1,3-DD-heptan, where the last DD-Hep residue of α1,3-DD-heptan is capped with β-GlcNAc residue.
In the structure as described above, the β-GlcNAc of the trisaccharide (α-DDHep-3-α-L-Fuc-3-β-GlcNAc), is linked to α-DDHep G. The α-DDHep of the trisaccharide is linked to the α1,6-glucan, which is in turn linked to the α1,3-DD-heptan. The α1,3-DD-heptan is then linked to a β-GlcNAc residue; the latter may provide a point of attachment for the O-chain polysaccharide. By the term “linked” or “substituted”, it is meant that the two moieties are joined by a covalent bond.
The term “α1,6-glucan” used herein may also be referred to interchangeably as “glucan”, “α1,6-glucan side chain”, “glucan side chain”, “α1,6-glucan moiety”, and/or “glucan moiety”. The α1,6-glucan is a linear polysaccharide chain of glucose monomers linked by α1,6-glycosidic bonds. In one example, which is not intended to be limiting in any manner, the α1,6-glucan may be a linear polysaccharide. The α1,6-glucan may comprise any suitable amount of α1,6-glucose residues. For example, and without wishing to be limiting in any manner, the glucan may comprise from about 3 to about 12 α1,6-linked glucose residues; specifically, the glucan moiety may comprise about 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 α1,6-linked glucose residues, or any range defined by any two values just recited.
In one non-limiting example, the α1,6-glucan may comprise 9-12 α1,6-glucose residues; in another non-limiting example, the α1,6-glucan may comprise 10 α1,6-glucose residues.
The term “glycoform” as used herein indicates different forms or types of the compound with the same LPS structure but differing in a number of α1,6-glucose or α1,3-heptose residues. For example, and without wishing to be bound by theory, each glycoform may comprise a specific length glucan and/or heptan moiety or a combination of thereof.
The term “α1,3-heptan” used herein may also be referred to interchangeably as “α1,3-DD-heptan”, “heptan”, “α1,3-heptan side chain”, “heptan side chain”, “α1,3-heptan moiety”, “heptan moiety”, and/or “DD-heptoglycan”. The α1,3-heptan is a polysaccharide chain of heptose monomers linked by α1,3 O-glycosidic bonds. In one example, which is not intended to be limiting in any manner, the α1,3-heptan may be a linear polysaccharide. The α1,3-heptan may comprise any suitable amount of α1,3-heptose residues. For example, and without wishing to be limiting in any manner, the heptan may comprise from about 2 to about 6 at 3-linked heptose residues; specifically, the heptan moiety may comprise about 2, 3, 4, 5, or 6 α1,3-linked heptose residues, or any range defined by any two values just recited.
The last DD-Hep residue of the α1,3-DD-heptan described above is capped with a β-GlcNAc residue. By the term “capped”, it is meant that the β-GlcNAc residue is the last residue in the side-chain; the term “terminated” may also be used. The β-GlcNAc may be linked to the DD-Hep via position 0-2 of the heptose. Without wishing to be bound by theory, the β-GlcNAc residue may provide a point of attachment for the O-chain polysaccharide.
In one non-limiting example, R may be
where β-GlcNAc residue L is linked to O-2 of Hep residue G. In this example, the β-GlcNAc residue W may provide a point of attachment for the O-chain polysaccharide. In the compound as just described, residues Q and Z of the glucan are α1,6-linked glucose residues, and n may be any value between about 1 to 11, such that the glucan comprises from about 3 to about 12 glucose residues in α1,6-linkage; in one specific, non-limiting example, a major glycoform contains 10 consecutive α1,6-linked glucose residues (n=9). In the compound as just described, residues T, Y, and X are α1,3-linked heptose residues, and m may be any value between about 0 to 4, such that the heptan comprises from about 2 to about 6 heptose residues in α1,3-linkage; in one specific, non-limiting example, a major glycoform contains 4 consecutive α1,3-linked heptose residues (m=2).
The structure may be isolated and/or purified from any suitable H. pylori strain; for example, and without wishing to be limiting in any manner, the truncated H. pylori LPS molecule may be isolated from a non-typeable H. pylori strain (i.e., one devoid of Lewis antigens), such as and not limited to a H. pylori strain having mutation in HP0826 gene leading to an isogenic mutant lacking O-chain polysaccharide. In a non-limiting example, the compound described herein may be isolated and/or purified from H. pylori strain 26695 HP0826::Kan or strain PJ2.
The structure of Formula I, also referred to herein as the “inner core molecule”, may further comprise a lipid A moiety covalently attached to a Kdo residue, for example the Kdo residue C. In other embodiments, the lipid A molecule may be O-deacylated or may be completely deacylated. In yet other embodiments, lipid A moiety may be cleaved through hydrolysis of the ketosidic linkage of the Kdo residue. Without wishing to be bound by theory, the cleavage of lipid A may be done to eliminate the toxicity of LPS and to avoid possible aggregation and insolubility of the conjugate. Persons of skill in the art would be familiar with methods for O-deacylation, deacylation, or hydrolysis of the ketosidic linkage of the lipid A moiety (see for example, Hoist et al., 1991; Altman et al., 2003).
The present invention also provides a conjugate comprising a substantially linear α1,6-glucan-containing compound conjugated to a protein carrier. The substantially linear α1,6-glucan-containing compound may be any suitable substantially linear polysaccharide comprised of α1,6-linked glucose residues. By the term “substantially linear”, it is meant that the α1,6-glucan contains few branches; for example, and without wishing to be limiting in any manner, the α1,6-glucan may comprise from about 0 to about 5% branching in the α1,6-glucan. Specifically, the α1,6-glucan may comprise about 0, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, or 5% branching, or any amount therebetween; the compound may also be a mixture, wherein the amount of branching within the mixture varies from one compound to another. In one non-limiting example, the α1,6-glucan-containing compound may be the structure as described above and herein. In another example, the α1,6-glucan-containing compound may be a Dextran. The Dextran may be any suitable Dextran that meets the requirements described above and having a molecular weight of between 1 and 10 kDa; for example but without wishing to be limiting in any manner, the Dextran may be about 1, 3.5, 5, 6.5, 8, or 10 kDa, or any value therebetween. In a specific, non-limiting example, the Dextran may be Dextran T5. In yet another example, the α1,6-glucan-containing compound may be a linear chain of between about 5 and 8 α1,6-linked glucose residues; for example, and without wishing to be limiting in any manner, the α1,6-glucan-containing compound may be a linear chain of 5, 6, 7, or 8 α1,6-linked glucose residues.
The α1,6-glucan-containing compound is conjugated to a linker molecule and/or a carrier protein; as would be understood by one of skill in the art, the structure described herein may be directly conjugated to the carrier protein, or may be conjugated to a linker molecule (also referred to herein as “linker”) that is in turn conjugated to the carrier protein. By the term “conjugated”, it is meant that the structure is covalently attached or linked to the linker molecule and/or carrier protein. Methods for covalent attachment of the linker and/or carrier protein are well-known to those of skill in the art; as would be appreciated by the skilled person, the method for covalent attachment (and whether or not a linker is present) may vary based on the carrier protein used. Without wishing to be limiting in any manner, one such method is shown in
The carrier protein may be any suitable carrier known in the art, including immunogenic carriers. For example, the carrier protein may be, but is not limited to tetanus toxoid, serum bovine albumin (BSA), Diphteria toxoid, mutant Diphteria toxoid, CRM, CRM197 protein, Pseudomonas A protein, Cholera toxin (CT) protein, a Cholera toxin mutant CT-E29H protein, and others known in the art for example but by no means limited to parts of flagella, pili and other toxins.
As previously indicated, conjugates could be prepared by either directly connecting the carrier protein and the structure of the present invention via naturally occurring groups or connecting via introduction of spacer or linker molecules, comprising but by no means limited to primary amino groups, hydrazides, thiols, carboxyls and others.
The present invention additionally provides a composition comprising one or more compounds as described herein, one or more conjugate as described herein, or a combination thereof. In one embodiment, the composition may comprise a mixture of glycoforms of the compound described above; for example, and without wishing to be limiting in any manner, the composition may comprise a major glycoform comprising 10 consecutive α1,6-linked glucose residues (n=9) in the glucan moiety. Similarly, and without wishing to be limiting in any manner, a composition could comprise conjugates prepared from more than one glycoform described herein. As demonstrated in the Examples, the LPS structure elaborated by H. pylori strain 26695 HP0826::Kan that was used for preparation of conjugates was a mixture of three glycoforms: backbone oligosaccharide I, backbone oligosaccharide I capped with GlcNAc and [GlcNAc, Fuc, Hep], and oligosaccharide containing α1,6-linked glucan, with the longest glucan chain corresponding to approximately twelve α-1,6-linked residues, as determined by CE-MS analysis (Table 2,
The composition as just described may be immunogenic. By the term “immunogenic”, it is meant that the composition may induce an immune response against H. pylori wild-type and/or mutant strains. The immune response may provide a broad immunogenic response against typeable and non-typeable strains of H. pylori.
The present invention also provides a use of an effective amount of the composition as described herein for inducing an immune response against H. pylori in an individual. As previously described, the composition may comprise one or more than one compound in accordance with the present invention. The one or more than one compound may be conjugated to a linker and/or a suitable carrier molecule.
The present invention further provides an immune antiserum produced by immunizing a mammal with the immunogenic composition as described above. The immune antiserum may comprise or yield a post-immune serum IgG recognizing an α1,6-linked glucan epitope in homologous and heterologous typeable and non-typeable mutant and wild-type strains of H. pylori. The IgG may cause complement-mediated bacteriolysis of mutant and wild-type α1,6-glucan-expressing H. pylori strains.
The present invention additionally provides anti-α1,6-glucan antibodies. The antibodies may be raised against the compound of the invention as described herein, or may be raised against other α1,6-glucan-containing molecules such as Dextran (or Dextran conjugates, for example but not limited to BSA-Dextran conjugates). In one non-limiting example, the antibody may be a monoclonal antibody, produced according to methods known in the art (see Example 10; Altman et al., 2005). For example, and without wishing to be limiting in any manner, the antibody may be a monoclonal antibody, raised against the α1,6-glucan epitope present in the outer core region of H. pylori HP0826 mutant LPS; more specifically, the antibody may be raised against the compound shown in
The present invention provides the use of 1C4F9 antibody to cause complement-mediated bacteriolysis of mutant and wild-type typeable and non-typeable α1,6-glucan-expressing H. pylori strains in an individual in need of such treatment. As previously described, typeable H. pylori strains have Lewis antigens recognized by anti-Le antibodies while non-typeable strains do not. However, since both typeable and non-typeable strains contain α1,6-glucan, both types of strains will be recognized by 1C4F9 antibody.
Currently in the art, H. pylori strains may be typed using commercially available antibodies against Lewis antigens; however, as non-typeable strains do not contain Lewis structures, they cannot be classified using this approach. As most typeable and non-typeable H. pylori strains carry α1,6-glucan epitopes, anti-α1,6-glucan antibodies (such as mAb 1C4F9) could provide an additional method of screening and characterizing H. pylori isolates.
The LPS of H. pylori strain 26695 HP0826::Kan was purified and its chemical structure determined by composition, methylation, in-depth nuclear magnetic resonance (NMR) analysis, as well as CE-MS data. The presence of α1,6-linked glucan in the outer core region of H. pylori HP0826 mutant LPS was also demonstrated; this structure was recognized by α1,6-glucan-specific monoclonal antibody, 1C4F9. The latter antibody was generated using formalin-fixed cells of H. pylori O:3 HP0826::Kan mutant strain. These antibodies were cell-surface accessible and bactericidal. Previously, it was believed that only the Lewis structures were antigenic; thus, the generation of antibodies against α1,6-glucan was unexpected.
To investigate the vaccine potential of H. pylori LPS, modified LPS of H. pylori 26695 HP0826::Kan mutant, was conjugated to tetanus toxoid (TT) or bovine serum albumin (BSA). Two approaches for preparation of the partially delipidated or delipidated LPS were utilised: O-deacylation of LPS by mild hydrazinolysis (LPS-OH) or delipidation of LPS by mild acid treatment (dLPS). Additional methods of delipidation and/or partial delipidation are well known in the art and such suitable methods may be used within the scope of the present invention. Both LPS-OH and dLPS were covalently linked through a 2-keto-3-deoxy-octulosonic acid (Kdo) residue to a diamino group-containing spacer, followed by the introduction of a maleimido functionality and conjugation to thiolated TT or BSA to give conjugates LPS-OH-TT, dLPS-BSA and dLPS-TT, respectively. In a separate experiment, non-typeable strain PJ2 was delipidated and utilised for conjugation to give dLPS(PJ2)-TT conjugate.
The LPS-OH-TT, dLPS-BSA, dLPS-TT conjugates as well as dLPS(PJ2)-TT retained antigenicity of the surface accessible α1,6-glucan determinant, as established by indirect ELISA with IgM 1C4F9. The antibody was shown to have excellent specificity for the α1,6-glucan determinant and its binding characteristics were determined by inhibition ELISA with oligosaccharides from isomalto-series and purified LPS from typeable and non-typeable strains of H. pylori. These studies confirmed that 1C4F9 had a requirement for 5 to 6 consecutive α1,6-linked glucose residues, a pattern consistent with the size of anti-α-(1→6)dextran combining sites postulated by Kabat (1993).
The LPS-OH-TT, dLPS-BSA, dLPS-TT or dLPS(PJ2)-TT conjugates were immunogenic in mice and rabbits and induced significant IgG antibody responses to LPS from homologous, heterologous, and wild-type strains of H. pylori. A ten-fold stronger IgG immune response to the immunizing antigen was generated in mice and rabbits that received dLPS-containing conjugate. The post-immune sera of rabbits immunized with either LPS-OH-TT, dLPS-BSA, dLPS-TT or dLPS(PJ2)-TT displayed bactericidal activity against 26695 HP0826::Kan mutant and the wild-type 26695 strains of H. pylori.
In summary, these results indicate that delipidated or partially delipidated H. pylori LPS-based protein conjugates devoid of Le antigen and carrying a long α1,6-glucan chain are immunogenic in both mice and rabbits and induce bactericidal antibodies. It is important to note that this epitope has been identified as being immunogenic. This was not established previously as only Lewis structures were known to be antigenic and to produce specific antibodies.
The present invention will be further illustrated in the following examples. However, it is to be understood that these examples are for illustrative purposes only and should not be used to limit the scope of the present invention in any manner.
Example 1: Isolation and Structural Analysis of H. pylori 26696 HP0826::Kan LPSHelicobacter pylori strain 26695 was obtained from Dr. R. Alm (Astra Zeneca, Boston, Mass.), H. pylori O:3 isolate was from Dr. J. Penner, J99 was obtained from Dr. D. Taylor (University of Alberta, Edmonton, Canada), SS1 from Dr. A. Lee (The University of New South Wales, Sydney, Australia), PJ1 and PJ2 clinical isolates were fresh clinical isolates from Dr. W. Conlan (IBS, NRC) and M6 was from Dr. K. Eaton (Michigan State University, MI).
Growth of bacterial strains was carried out as described by Hiratsuka et al. (2005). Briefly, cells were grown at 37° C. on antibiotic-supplemented Columbia blood agar (DIFCO™) plates containing 7% horse blood in microaerophilic environment for 48 h (Kan 20 μg/mL) as previously described (Hiratsuka et al., 2005). For growth in liquid culture, antibiotic supplemented Brucella broth containing 10% fetal bovine serum was inoculated with H. pylori cells harvested from 48 h Columbia blood agar/horse blood plates and incubated for 48 h in a shaker under microaerophilic conditions (85% N2, 10% CO2, 5% O2) as previously described (Hiratsuka et al., 2005).
H. pylori strains were cultivated in liquid culture as described above, and the wet cell mass obtained by centrifugation of the bacterial growth was washed twice successively with ethanol, acetone and light petroleum ether and air-dried. LPS was extracted from the air-dried cellular mass by hot phenol-water extraction procedure of Westphal and Jann (1965). LPS was obtained from the aqueous phase after extensive dialysis and lyophilization. H. pylori LPS was further purified by ultracentrifugation (105,000×g, 4° C., 12 h), and the pellet was suspended in distilled water and lyophilized.
Sugar composition analysis was performed by the alditol acetate method (Sawardeker et al., 1967). The hydrolysis was done in 4 M trifluoroacetic acid at 100° C. for 4 h or 2 M trifluoroacetic acid at 100° C. for 16 h followed by reduction in H2O with NaBH4 and subsequent acetylation with acetic anhydride/pyridine. Alditol acetate derivatives were analyzed as previously described (Altman et al., 2003). Methylation analysis was carried out according to the method of Ciucanu & Kerek (1984) and with characterization of permethylated alditol acetate derivatives by gas liquid chromatography-mass spectrometry (GLC-MS) as previously described (Altman et al., 2003).
Sugar analysis of purified LPS from H. pylori 26695 HP0826::Kan as alditol acetates revealed the presence of L-fucose (L-Fuc), D-glucose (D-Glc), D-galactose (D-Gal), N-acetyl-D-glucosamine (D-GlcNAc), D-glycero-D-manno-heptose (DD-Hep) and L-glycero-D-manno-heptose (LD-Hep) in the approximate molar ratio of 0.4:5.0:1.5:4.3:6.4:1.4, indicating the presence of the structure devoid of O-chain (Logan et al., 2000). Methylation analysis carried out on the intact 26695 HP0826::Kan LPS was consistent with these findings and showed the presence of terminal L-Fuc, 3-substituted L-Fuc, terminal D-Glc, terminal D-Gal, 3-substituted glucose, 4-substituted D-Gal, 6-substituted glucose, terminal DD-Hep, 2-substituted DD-Hep, 6-substituted DD-Hep, 3-substituted DD-Hep, 7-substituted DD-Hep, 2,7-substituted DD-Hep, 2-substituted LD-Hep, 3-substituted LD-Hep, terminal D-GlcNAc and 3-substituted D-GlcNAc in the approximate molar ratio of 0.11.0:1.1:0.1:1.2:1.0:6.0:0.41.2:1.1:3.1:0.5:1.61.2:0.1:0.3:0.4. No 3,4-substituted D-GlcNAc and 2-linked D-Gal, characteristic of the O-chain containing Le antigens, were detected. The purity of LPS was confirmed by the absence of RNA derived ribitol. Composition and methylation analyses of 26695 LPS have been reported elsewhere (Logan et al., 2005). All sugars were present in the pyranose form.
Example 2: Characterization of Delipidated H. pylori 26695 HP0826::Kan LPS by Capillary Electrophoresis-Mass Spectrometry (CE-MS)Purified 26695 HP0826::Kan LPS (20 mg) obtained in Example 1 was hydrolyzed in 0.1 M sodium acetate buffer, pH 4.2, for 2 h at 100° C. and fractionated by gel filtration on a BID-GEL™ P-2 column as described previously (Altman et al., 2003) to generate delipidated LPS (dLPS). Three fractions (fractions 1-3) were collected and analyzed by capillary electrophoresis mass spectrometry (CE-MS; Table 1).
For CE-MS, a PRINCE™ CE system (Prince Technologies, The Netherlands) was coupled to a 4000 QTRAP mass spectrometer (APPLIED BIOSYSTEMS™/MDS SCIEX™, Canada). A sheath solution (isopropanol-methanol, 2:1) was delivered at a flow rate of 1.0 μL/min. Separations were obtained on about 90 cm length bare fused-silica capillary using 15 mM ammonium acetate in deionized water, pH 9.0. The 5 kV electrospray ionization voltage was used for the positive ion detection mode. Tandem mass spectra were obtained using enhanced production ion scan mode (EPI) with a scan rate of 4000 Da/s. Nitrogen was used as curtain (at a value of 12) and collision gas (set to scale “high”).
CE-MS analysis of the major fraction 1 in the positive ion mode confirmed the presence of a series of triply charged ions at m/z 1212.3, m/z 1266.3 and m/z 1320.4 consistent with consecutive additions of Hex residues, the longest glucan chain corresponding to approximately eleven α-1,6-linked residues. Based on the signal intensity of ions, the most abundant glycoform at m/z 1266.3 contained ten α-1,6-linked Hex (
O-Deacylation of 26695 HP0826::Kan LPS (of Example 1) was carried out according to Hoist et al. (1991) with some modifications. Briefly, LPS (4 mg) was stirred in anhydrous hydrazine (0.2 ml) at 37° C. for 4 h. The reaction mixture was cooled, and cold acetone (2 ml) was slowly added to destroy excess hydrazine. After 30 min, precipitated O-deacylated LPS (LPS-OH) was collected by centrifugation (4° C., 9300×g, 10 min). The pellet was washed twice with cold acetone, dissolved in water and lyophilized to give LPS-OH (3.5 mg).
CE-MS analysis of the 0-deacylated 26695 HP0826::Kan LPS (LPS-OH) in the positive ion mode was performed as described in Example 2. Results of CE-MS were consistent with MS data obtained for delipidated LPS and afforded three major doubly charged ions at m/z 1137.2, m/z 1239.2 and m/z 1408.0 consistent with the presence of the backbone oligosaccharide and backbone oligosaccharide capped with HexNAc and [HexAc, Fuc, Hep], respectively (Table 2), while triply charged ions at m/z 1597.7, m/z 1651.4 and m/z 1705.5 were consistent with the presence of glucan, the longest glucan chain corresponding to approximately twelve α-1,6-linked residues (Table 2,
Degradation of the LPS from H. pylori strain 26695 HP0826::Kan (of Example 1) was initiated with complete deacylation with 4 M KOH in the presence of NaBH4 for the instant reduction of lipid A GlcN, since alkaline hydrolysis of PEtN substituent leaves reducing end GlcN without aglycon (Holst et al., 1991). Separation of the products by gel chromatography gave two fractions, eluted in the oligosaccharide region of the chromatogram. Further analysis showed that these fractions contained similar compounds, apparently differing by the length of a glucan chain. Lower molecular mass fraction contained compounds 1-3, identified by mass spectrometry, and both fractions contained compound 4 with different length of glucan portion (
NMR spectra (DQCOSY, TOCSY, NOESY, 1H-13C HSQC and HMBC) were performed on a VARIAN™ 500 or 600 MHz spectrometer using standard software as described previously (Brisson et al., 2002). All NMR experiments were performed at 25° C. using acetone as an internal reference at δ 2.225 ppm for 1H spectra and 31.45 ppm for 13C spectra.
NMR spectra of both fractions corresponded to compound 4, although spectra could not be completely interpreted due to their complexity. The H-1 protons of terminal residues of α-1,6-glucan and DD-heptan did not overlap with the rest of glucan and heptan H-1, thus allowing identification of the position of these homopolymers within the entire structure, as shown in
For further analysis of the LPS structure compounds 1-4 were deaminated. Briefly, the samples were dissolved in 10% AcOH and an excess of NaNO2 was added; after 3 h, product was isolated by gel chromatography on SEPHADEX™ G-15 column. Some compounds were then reduced with NaBD4 and desalted. The resulting products were compounds 5 and 6. NMR spectra of compound 5 (performed as described above) showed two isomers with phosphate at position 6 or 7 of the Hep E (due to phosphate migration under alkaline conditions). Again, three contiguous Hep residues were present, not four as would have been expected if the previously proposed structure were correct. Removal of the entire side chain by deamination procedure (described above) confirmed that GlcN L formed the connection between sugars of the OS 5 and the remainder of the molecule.
Compound 6 contained DD-heptan, α-1,6-glucan and trisaccharide DDHep-Fuc-anh-Man-ol (N-M-L, anh-Man L deriving from GlcN L) at the reducing end. Spectra of this product were less crowded and it became possible to identify the attachment point of the α-1,6-glucan to O-6 of the DDHep N (from TOCSY between H-1 and H-6 of DDHep N). The structure was linear, as confirmed by methylation analysis, which showed no branched sugars; all expected products were identified in agreement with the proposed structure (Table 4).
Further confirmation of the structure of DD-heptan-α-1,6-glucan region was obtained from the results of the periodate oxidation of compound 6. Periodate oxidation was performed with an excess of 0.1 M NaIO4 for 24 h; ethyleneglycol was added and product isolated by gel chromatography on SEPHADEX™ G-15 column. It was reduced with NaBD4, desalted, and hydrolyzed with 2% AcOH for 3 h at 100° C. Two main products, 7 and 8, were obtained and isolated by gel chromatography on SEPHADEX™ G-15 column.
The reduction of oxidized oligosaccharide with NaBD4 allowed identification of the oxidized carbons in NMR spectra (inverted phase of CHDOH signals as compared with CH2OH signals in APT-HSQC). The structure of compounds 7 and 8 was determined by NMR spectroscopy and methylation analysis. Formation of compound 7 proved that DDHep N was not substituted at position 3. Since methylation of compound 6 showed only terminal, 3- and 6-substituted DD-Hep, DD-Hep N was substituted at position 6, as it was proposed from NMR data of compound 6. Formation of compound 8 with glycerol (Gro) at the reducing end confirmed that Glc V in the OS 6 glycosylated next Glc residue at position 6, since there were no other components of the oligosaccharide 6 which could produce glycerol upon oxidation-reduction. It also clearly proved the attachment of the DD-heptan moiety to the non-reducing end of α-1,6-glucan at position 3 of terminal glucose.
The size of the DD-heptan domain could be estimated: compound 8 contained four mannose residues, derived from DD-heptose. Spectra of compound 8 were well resolved and integration of H-1 signals gave nearly equimolar ratio and showed the presence of four mannose residues. Thus, the intact DD-heptan domain in compound 6 consisted mostly of 5 DD-heptose units, one of which (terminal) was removed by periodate oxidation. This conclusion was confirmed by mass spectrometry. The structure of the major LPS glycoform produced by H. pylori strain 26695 HP0826::Kan is illustrated in
Kdo-linked conjugates of LPS-OH (see Example 3) and dLPS (see Example 2) to bovine serum albumin (BSA) and/or tetanus toxoid (TT) were prepared.
LPS-OH (4 mg, 0.8 μmol, based on an estimated average molecular mass of 4789 Da) or dLPS (4 mg, 1 μmol, based on an estimated average molecular mass of 3779 Da) was dissolved in 0.1 M 2-(N-morpholino)ethanesulfonic acid (MES; SIGMA-ALDRICH™, St. Louis, Mo.) buffer, pH 4.8, containing 0.1 M NaCl (0.4 mL); 1-ethyl-3-dimethylaminopropyl carbodiimide (EDC; 34.38 mg, 100:1 molar ratio; SIGMA-ALDRICH™) was added followed by 1,8-diamino-3,6-dioxaoctane (15 μL, 103 μmol; SIGMA-ALDRICH™), and the reaction was maintained at pH 4.8 for 4 h at 22° C. The solution was adjusted to pH 7.0 and dialyzed against distilled water or desalted using a MICROSEP™ centrifugal device, 1,000 Da cutoff (PALL LIFE SCIENCES™, Ann Arbor, Mich.) and lyophilized.
The conjugation procedure was carried out essentially as described for oligosaccharides by Fernandez-Santana et al. (1998). Briefly, the spacer-containing LPS-OH (2 mg, 0.4 μmol) or dLPS (2 mg, 0.5 μmol) was reacted with 3-maleimidopropionic acid N-hydroxysuccinimide ester (BMPS; 2 mg, 7.5 μmol; SIGMA-ALDRICH™) in dry DMSO for 24 h at 22° C. The solution was dialyzed against distilled water, and lyophilized.
For activation of BSA, 3,3′-dithiodipropionic acid di(N-hydroxysuccinimide ester) (DTSP; 0.63 mg, 1.6 μmol; SIGMA-ALDRICH™) in dry DMSO, was added, under N2 atmosphere, to a solution of bovine serum albumin (BSA) (molecular mass 66,320 Da) (8 mg, 0.12 μmol) previously dissolved in 10 mM PBS buffer, pH 8.0, containing 6 mM EDTA (final concentration 4 mg/mL), and the mixture was stirred for 2 h at 22° C. This was followed by addition of dithiothreitol (DTT; 7.12 mg, 46 μmol; SIGMA-ALDRICH™), under N2 atmosphere, and the mixture was stirred for 1 h at 4° C. The resulting solution was dialyzed against 10 mM PBS buffer, pH 7.2, containing 5 mM EDTA in a stirred ultrafiltration cell (MILLIPORE™, Billerica, Mass.), using N2 as a pressure source, over a regenerated cellulose membrane, 30,000 Da cutoff (YM30, MILLIPORE™) at 4° C. The protein and SH contents were determined by bicinchoninic acid protein assay kit (BCA; PIERCE™, Rockford, Ill.) and Ellman (1959) methods, respectively. A molar substitution of 20-22 SH groups was attained.
For the activation of tetanus toxoid (TT) (molecular mass, 150,000 Da), DTSP (0.316 mg, 0.8 μmol) in dry DMSO (25 μL) was added, under N2 atmosphere, to a solution of TT (4 mg, 0.03 μmol) in 10 mM PBS buffer, pH 8.0, containing 6 mM EDTA (final concentration 4 mg/mL), and the reaction was allowed to proceed as described for BSA. This was followed by addition of dithiothreitol (DTT; 3.56 mg, 23 μmol; SIGMA-ALDRICH™), under N2 atmosphere, and the mixture was stirred for 1 h at 4° C. Activated TT was transferred to a stirred ultrafiltration cell (MILLIPORE™) and dialyzed against 10 mM PBS buffer, pH 7.2, containing 5 mM EDTA over a regenerated cellulose membrane, 100,000 Da cutoff (YM100, MILLIPORE™) at 4° C.
To a solution of BSA-SH21-22 or TT-SH21-22 in 10 mM PBS buffer, pH 7.2, containing 5 mM EDTA, a solution of maleimido-functionalized LPS-OH or dLPS derivative in 10 mM PBS buffer, pH 7.2, containing 5 mM EDTA (final concentration 4 mg/mL) (3:1 molar ratio) was added under N2 atmosphere. The reaction was stirred for 24 h at 4° C. This was followed by addition of N-ethylmaleimide (1 mg; SIGMA-ALDRICH™). The reaction was allowed to proceed for 30 min at 22° C., and the resulting conjugate was dialyzed against 10 mM PBS buffer, pH 7.2, for 4 d at 4° C. and filter sterilized using 0.22 μm polyvinylidene fluoride (PVDF) membrane (MILLIVEX-GV™, MILLIPORE™, Cork, Ireland). Conjugates were analyzed for their carbohydrate and protein content using phenol sulfuric acid method for neutral sugars (Dubois et al., 1956) and BCA protein assay kit (PIERCE™), respectively, with LPS-OH or dLPS and BSA as standards. The efficiency of conjugation was confirmed by high performance liquid chromatography (HPLC; AGILENT 1200 SERIES™, AGILENT TECHNOLOGIES™ Waldbronn, Germany) using SUPEROSE™ 12 10/300 GL column (AMERSHAM BIOSCIENCES™, Uppsala, Sweden) equilibrated with 10 mM PBS buffer pH 7.2. The chromatography was carried out at room temperature and at a flow rate 0.5 mL/min. The elution was monitored at 210 nm and 280 nm with diode array detector (AGILENT TECHNOLOGIES™).
The presence of a spacer was confirmed by 1H-NMR spectroscopy by the appearance of a new proton resonance at 3.22 ppm, corresponding to CH2NH2 group. The amine group of the spacer molecule was further derivatized by reaction with 3-maleimidopropionic acid N-hydroxysuccinimide ester to yield maleimido-functionalized LPS-OH or dLPS, as confirmed by the presence of proton resonances at 2.55 ppm and 6.9 ppm, corresponding to CH2α and CH═CH groups of β-maleimidopropionate, respectively (
The molar ratio of LPS-OH to TT in three conjugates ranged from 10:1 to 20:1, and the yield ranged from 13% to 22%, based on the carbohydrate content (Table 5). Conjugation of dLPS to BSA or TT yielded dLPS-BSA-2, dLPS-TT or dLPS(PJ2)-TT conjugates with significantly higher carbohydrate content (Table 5). Both LPS-OH-TT and dLPS-BSA or dLPS-TT conjugates reacted equally well with α1,6-glucan-specific mAbs by ELISA suggesting that the conformation of the glucan epitope was unchanged.
The immunogenicity of the conjugates (LPS-OH-TT, dLPS-BSA, dLPS-TT, and dLPS(PJ2)-TT) of Example 5 was tested in mice and rabbits.
Five 6-8 week old female BALB/c mice were immunised intraperitoneally with appropriate conjugates. Each mouse received 2 μg or 10 μg of carbohydrate in 0.2 mL Ribi adjuvant per injection. The mice were boosted on day 21 and 42 and sera recovered after terminal heart puncture on day 51.
Three New Zealand white rabbits were immunised subcutaneously with appropriate conjugates. Each rabbit received 10 μg or 50 μg of carbohydrate in 0.5 mL Incomplete Freunds adjuvant. The rabbits were boosted on day 28 and 56 and sera recovered after exsanguination on day 65.
The level of anti-LPS antibody in serum was measured by ELISA in which purified LPS was used as a coating antigen (1 μg/well). After washing with PBS, the plates were blocked with 1% (w/v) bovine serum albumin (BSA) in PBS or Milk Diluent/blocking solution (MDB) (KPL™, Gaithersburg, Md.) for 1 h at 37° C. Diluted mouse or rabbit pre- or post-immune sera were added, and the plates were incubated for 2 h at 37° C. For inhibition ELISA, serial dilutions of inhibiting 26695 HP0479::Kan LPS or 26695 HP0826::Kan LPS were mixed with previously determined dilution of rabbit sera that gave OD450=0.6-0.8. This mixture was incubated for 15 min at 22° C. and then transferred to the original microtiter plate blocked with adsorbed LPS antigen, where it was incubated for another 2 h at 37° C. After this step, the indirect ELISA procedure was followed. Briefly, the plates were washed with PBS and the second antibody, a goat anti-mouse IgG+IgM horseradish peroxidase conjugate (CALTAG™, So. San Francisco, Calif.) was added for 1 h at room temperature. After a final washing step, 3,3′,5,5′-tetramethylbenzidene (TMB) (KPL™, Gaithersburg, Md.) substrate was added and the reaction was stopped with 1 M phosphoric acid. The absorbance was determined at 450 nm using a microtiter plate reader (DYNATECH™, Chantilly, Va.).
The percentage inhibition was calculated using the following formula:
% inhibition=100×[(OD with inhibitor−OD without inhibitor)/OD without inhibitor]
Inhibition versus log concentration curves were plotted for each inhibitor, and the concentrations required for the half maximal inhibitory concentration (IC50) were determined from extrapolation curves.
All conjugates elicited an IgG response against LPS from the homologous (26695 HP0826::Kan) and corresponding wild-type (26695) strains in both rabbits and mice after three injections (Tables 6 to 9) although the response was generally weaker in LPS-OH-TT immunized mice and rabbits than in animals immunized with either dLPS-BSA, dLPS-TT or dLPS(PJ2)-TT. Control rabbits immunized with a mixture of either LPS-OH, dLPS or dLPS(PJ2) and a protein carrier (with an adjuvant) showed no or low level specific response to LPS from the homologous strain (26695 HP0826::Kan mutant) or corresponding wild-type 26695 strain of H. pylori after three immunizations.
Cross-reactivity studies were performed with the post-immune sera of rabbits immunized with either LPS-OH-TT-2, LPS-OH-TT-3, LPS-OH-TT-4, dLPS-BSA-2, dLPS-TT, or dLPS(PJ2) against LPS from H. pylori strains representative of various LPS glycotypes (Monteiro, 2001) and selected mutant strains. Results are shown in Tables 10, 11 and 12.
The reactivity of post-immune sera obtained from rabbits that were immunized with LPS-OH-TT-2, LPS-OH-TT-3, or LPS-OH-TT-4 was indicative of the requirement for the presence of α1,6-glucan since only weak cross-reactivity was obtained with SS1 and SS1 HP0826::Kan LPS, these being representative of H. pylori strains unable to add α1,6-glucan (Logan et al., 2005) (Table 10). Surprisingly, sera obtained from rabbits that were immunized with dLPS-TT also recognized core LPS epitopes that did not contain any α1,6-glucan, namely LPS from strains SS1, SS1 HP0826::Kan, M6 and J99 (Table 11), showing a broader core recognition and inferring that dLPS-TT conjugate was more immunogenic, possibly due to the presence of TT carrier protein (Table 11). Alternatively, as the conjugates were prepared from a mixture of 3 glycoforms, the immune response may have been generated to other minor LPS components; this could explain the observed cross-reactions.
To probe the binding specificity of rabbit sera elicited by dLPS-TT conjugate, inhibition ELISA was conducted with purified 26695 HP0479::Kan LPS consisting of two glycoforms (approx. ratio 1:1), a linear backbone oligosaccharide structure and a linear backbone oligosaccharide capped with [GlcNAc, Fuc] (Hiratsuka et al., 2005), and 26695 HP0826::Kan LPS. Binding of rabbit sera to glucan-negative LPS from strains SS1, SS1 HP0826::Kan HP0159::Kan and SS1 HP0479::Kan (
The ability of rabbit post-immune sera to recognize heterologous typeable and non-typeable strains was also validated in the whole cell indirect ELISA (WCE) against selected clinical isolates of H. pylori representatives of both typeable and non-typeable strains of H. pylori. The whole-cell indirect ELISA (WCE) was performed as previously described (Altman et al., 2008). Briefly, the wells of a microtiter plate were coated with 100 μL of a bacterial suspension, 108 cells/mL, overnight, at 4° C. The wells were then fixed with methanol and blocked with 200 μL of Milk Diluent/Blocking solution (MDB) (KPL™, Gaithersburg, Md.) for 2 h at 37° C. Subsequently, the wells were incubated for 2 h at 37° C. with 100 μL of 1C4F9 ascites diluted 1:500 in MDB, followed by anti-mouse IgG+IgM horseradish peroxidase (CALTAG™) diluted 1:1,000 in MDB for 1 h at room temperature. The substrate TMB was added as described for indirect ELISA. The non-specific background values were determined as OD450 of the negative control wells containing bacterial cells, secondary antibody conjugate and substrate. These OD450 values were ≦0.2. The optical density values of OD450<0.2 were classified as negative and OD450 values≧0.2 were classified as positive reactions. To ensure plate to plate consistency H. pylori strain 26695 cells were used as a positive control. Assays did not vary by more than 10%.
Sera derived from rabbits that were immunized with dLPS-TT conjugate showed the strongest cross-reactivity to all strains tested (Table 13) using whole cell indirect ELISA.
A bactericidal assay using pre- or post-vaccinated rabbit sera (Example 6) was performed.
Plate-grown H. pylori cells were harvested and washed with 5 mL of PBS per plate. Following centrifugation, pellets were suspended in 25 mL of PBS. The final bacterial suspension was diluted in Dulbecco's phosphate-buffered saline (DPBS) (INVITROGEN™, Grand Island, N.Y.) at 4×106 CFU/mL. The bactericidal assay was performed in a flat-bottomed microtiter plate (ICN). A ten-fold serial dilution of de-complemented pre- or post-immune sera (50 μL) was added to each well. Bacterial suspension (25 μL) was then added and pre-incubated for 15 min at 37° C. Baby rabbit complement (CEDARLANE LABORATORIES™, Hornby, ON) was diluted 1:50 and 25 μL was added to the appropriate wells. The plate was incubated for 45 min at 37° C. and then placed on ice. A 10 μL aliquot was plated in triplicate on Columbia blood agar, grown for 4 days, and then the plates were counted to measure the number of colony forming units (CFU). The control plate with bacteria and complement but without sera was used to calculate the percentage killing. The bactericidal activity was determined as the highest dilution of sera that caused 50% killing.
Pre-vaccination sera or sera obtained from rabbits immunized with a mixture of a protein carrier and either LPS-OH, dLPS, or dLPS(PJ2) (with an adjuvant) showed no or low levels of bactericidal activity against the homologous H. pylori 26695 HP0826::Kan or wild-type 26695 strains. The post-immune sera obtained from rabbits immunized with LPS-OH-TT-4, dLPS-BSA-2, dLPS-TT and dLPS(PJ2)-TT showed significant functional activity against both 26695 HP0826::Kan mutant and corresponding wild-type strains (Table 14) with postvaccination sera from rabbits immunized with dLPS-TT conjugate exhibiting the highest functional activity against wild-type strain 26695 (Table 14).
Furthermore, bactericidal activity of the rabbit sera was also tested against selected clinical isolates of H. pylori, namely strains 002CL, 0153CL and 058CL (Altman et al., 2008). These isolates were selected as representatives of high, medium and low binders based on their OD450 values in WCE assays with anti-α1,6-glucan mAbs: strain 002CL-OD450 1.361, high binder; strain 153CL-OD450 0.29, medium binder; and strain 058CL-OD450 0.162, low binder. It is important to emphasize that only the post-immune sera from rabbits immunized with either dLPS-TT or dLPS(PJ2)-TT conjugate showed functional activity with all three clinical isolates tested (Table 15).
The potential of dLPS-TT conjugate as a candidate vaccine was evaluated in outbred CD-1 mice.
Groups of 5 CD-1 mice were vaccinated four times intranasally at weekly intervals with 25 μg/mouse dLPS-TT conjugate, adjuvanted with 1 μg/mouse cholera toxin (CT; SIGMA™), 31.5 μg/mouse PJ2 cell-free sonicate adjuvanted with 1 μg/mouse cholera toxin (control), or saline (control). One week after the last immunization, serum, fecal and vaginal wash samples were collected and assayed for H. pylori-specific IgG and IgA. Serum IgG and serum, fecal and vaginal IgA antibody levels were determined by standard ELISA. Plates were coated with 1 μg/well H. pylori strain 26695 HP0826::Kan LPS as described herein. Serum samples were diluted 1:100 for IgG and 1:50 for IgA assay. Fecal samples were diluted 1:2 and vaginal samples were diluted 1:20. H. pylori-specific antibody levels were determined and the data was analyzed by Mann-Whitney analysis, using GRAPHPAD™ software version 5.0.
Five weeks after the first immunization, mice were orally gavaged three times every other day with ˜108 cfu H. pylori strain PJ2 (Altman et al., 2003). Four weeks later, mice were killed and viable bacteria from their stomachs were enumerated and the data were analyzed by Mann Whitney test, using GraphPad software version 5.0.
Intranasal immunization with dLPS-TT conjugate plus CT elicited a very strong H. pylori 26695 HP0826::Kan LPS-specific IgG response as measured by ELISA and moderate H. pylori 26695 HP0826::Kan LPS-specific serum IgA was also detected (Tables 16 and 17,
All groups of mice were subsequently inoculated orogastrically with non-typeable H. pylori mouse-colonizing strain PJ2 previously shown to contain a long α1,6-glucan (Altman of al., 2003). Protection is defined as statistically significant decrease in bacterial load in vaccinated groups compared to control groups. The colonization data for groups of mice immunized intranasally with dLPS-TT conjugate plus CT was statistically significant (p<0.05) (
Dextran-BSA conjugate was prepared by dissolving 10 mg Dextran T5 (MW 5 KDa, PHARMACOSMOS A/S™, Holbaek, Denmark) in 250 μL of 0.2 M borate buffer, pH 9.0; this was added to a solution (250 μL) containing 1,8-diamino-3,6-dioxaoctane (25 μL) and sodium cyanoborohydride (10 mg) in 0.2 M borate buffer, pH 9.0 (as described by Roy et al., 1984). The reaction was carried out for 5 days at 55° C. The reaction product was purified as described above for preparation of LPS-based conjugates.
This reaction results in the introduction of a spacer. The amine group of the spacer molecule was further derivatized by reaction with 3-maleimidopropionic acid N-hydroxysuccinimide ester as described for LPS-based conjugates (see Example 5). The glycoconjugate was obtained through thiolation of a carrier protein and addition of the thiolated protein to the maleimido-functionalized Dextran T5. The molar ratio of Dextran to BSA in the conjugate was 20:1, and the yield was 32%, based on the carbohydrate content.
Cross-reactivity studies were performed with post-immune sera of rabbits immunized with Dextran-BSA against LPS from H. pylori strains representative of various LPS glycotypes and selected mutant strains (Table 18).
The reactivity of post-immune sera obtained from rabbits that were immunized with Dextran-BSA was indicative of the requirement for the presence of α1,6-glucan since no cross-reactivity was obtained with glucan-negative strains SS1 and SS1 HP0826::Kan. The post-immune sera obtained from rabbits immunized with Dextran-BSA showed functional activity against both 26695 HP0826::Kan mutant and corresponding wild-type strain (Table 19).
The ability of rabbit post-immune sera to recognize heterologous typeable and non-typeable strains and induce bactericidal antibodies indicates the possibility that a conjugate consisting of Dextran, a polymer containing a linear backbone of α1,6-linked glucose repeating units, or a conjugate comprising optimized linear oligosaccharide/s consisting of consecutive α1,6-linked glucose residues, and a suitable protein carrier could be sufficient to confer protection against H. pylori infection.
Example 10: Specificity Studies of Anti-Glucan mAbsMonoclonal antibodies specific to H. pylori strain O:3 HP0826::Kan were produced and their specificities studied.
Hybridomas were produced as previously described (Altman et al., 2005). Six BALB/c mice (Charles River Laboratories, St Constant, QC) were injected intraperitoneally (i.p.) with 108 cells (200 μL) formalin fixed cells of H. pylori strain O:3 HP0826::Kan 5 times over 82 days to achieve significant titer. A final intravenous (i.v.) injection was given and was followed 3 days later by fusion. The spleen cells of two mice were fused with an Sp2/O plasmacytoma cell line according to Kohler and Milstein (1975). Initial fusion supernatants from 368 wells were screened by indirect enzyme-linked immunosorbent assay (ELISA).
For hybridoma screening by ELISA, microtiter plates (ICN™, Costa Mesa, Calif.) were coated with 10 μg/mL of corresponding H. pylori 0:3 HP0826::Kan LPS in 50 mM carbonate buffer, pH 9.8, for 3 h at 37° C. After washing with PBS, the plates were blocked with 5% (w/v) bovine serum albumin (BSA) in PBS. Spent supernatants were added, and the plates were incubated for 3 h at room temperature. The plates were washed with PBS and the second antibody, a goat anti-mouse IgG+IgM horseradish peroxidase conjugate (CALTAG™, So. San Francisco, Calif.) was added for 1 h at room temperature. After a final washing step, 3,3′,5,5′-tetramethylbenzidene (TMB) (KPL™, Gaithersburg, Md.) substrate was added, and the reaction was stopped with 1 M phosphoric acid. The absorbance was determined at 450 nm using a microtiter plate reader (DYNATECH™, Chantilly, Va.). After this step, the indirect ELISA procedure was followed as described in Example 6.
Two stable hybridomas were obtained following limited dilution cloning. One clone, 1C4F9, an IgM, was selected for further characterization. Ascitic fluid was raised in BALB/c mice, and 1C4F9 monoclonal antibody (mAb) was purified from ascitic fluid using an IgM-specific affinity column (PIERCE™, Rockford, Ill.) according to the manufacturer's protocol.
Studies of the specificity of the glucan-specific antibody were carried out using a series of linear oligosaccharides consisting of consecutive α1,6-linked glucose residues Glc→[α(1→6)Glc]n=1-6 and selective purified H. pylori LPS. For inhibition ELISA, serial dilutions of linear α1,6-linked glucose-containing oligosaccharides from isomalto-series [Glcα1→(6Glcα1→)n=1-6] (USBIOLOGICALS™, Swampscott, Miss.) or H. pylori 26695, O:3 and PJ2 LPS inhibitors were prepared and mixed with previously prepared dilutions of purified 1C4F9 that gave an OD450=1. Following the incubation (22° C., 15 min), this mixture was transferred to the original blocked microtiter plate with adsorbed LPS antigen, where it was incubated for another 2 h at 37° C. After this step, the indirect ELISA procedure was followed as described in Example 6. The percentage inhibition was calculated using the following formula:
% inhibition=100×[(OD with inhibitor−OD without inhibitor)/OD without inhibitor]
Inhibition versus log concentration curves were plotted for each inhibitor, and the concentrations required for the half maximal inhibitory concentration (IC50) were determined from extrapolation curves.
The inhibitory properties optimized when using isomaltohexaose (n=5) and isomaltoheptaose (n=6) (Table 20). H. pylori PJ2 LPS previously shown to contain on average between six and eight residues in the glucan chain (Altman et al., 2003) was the most effective inhibitor (Table 20).
Anti-glucan mAbs were readily accessible on the surface of live bacteria from representative H. pylori strains as demonstrated by indirect IF microscopy studies (Table 21). Both α1,6-glucan and CagA could be differentiated on the bacterial surface simultaneously.
To determine bactericidal activity of the monoclonal antibody, a ten-fold serial dilution of 1C4F9 mAb from de-complemented ascites (50 μL) was added to each well followed by bacterial suspension (25 μL) and pre-incubated for 15 min at 37° C. After this step, the procedure was followed as described in Example 7. The cell surface binding of 1C4F9 correlated with functional activity as determined by bactericidal assays against wild-type and mutant strains of H. pylori (Table 21).
While the preferred embodiments of the invention have been described above, it will be recognized and understood that various modifications may be made therein, and the appended claims are intended to cover all such modifications which may fall within the spirit and scope of the invention.
REFERENCESAll patents, patent applications and publications referred to herein and throughout the application are hereby incorporated by reference.
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Claims
1. An immune antiserum isolated from an individual comprising antibodies recognizing an α1,6-glucan-containing Helicobacter pylori compound comprising the structure of Formula I: wherein the R is a α-DDHep-3-α-L-Fuc-3-β-GlcNAc trisaccharide substituted with an α1,6-glucan comprising from 4 to 12 α1,6-linked glucose residues linked to an α1,3-DD-heptan, wherein the last DD-Hep residue of the α1,3-DD-heptan is capped with β-GlcNAc residue.
2. The immune antiserum of claim 1, wherein in the structure of Formula I, the heptan moiety comprises from 2 to 6 α1,3-linked heptose residues.
3. The immune antiserum of claim 1, wherein in the structure of Formula I, R comprises where β-GlcNAc residue L is linked to O-2 of Hep G, n=1 to 11, and m=0 to 4.
4. The immune antiserum of claim 3, wherein in the structure of Formula I, n=9.
5. The immune antiserum of claim 3, wherein in the structure of Formula I, m=2.
6. The immune antiserum of claim 1, wherein the structure of Formula I further comprises a lipid A moiety covalently attached to the Kdo residue C.
7. The immune antiserum of claim 6, wherein in the structure of Formula I, the lipid A molecule is O-deacylated or is cleaved through hydrolysis of the ketosidic linkage of the Kdo residue.
8. The immune antiserum of claim 1, wherein the compound is isolated or purified from H. pylori strain HP0826::Kan.
9. The immune antiserum of claim 1, the antiserum comprising an IgG recognizing an α1,6-linked glucan epitope in homologous and heterologous typeable and non-typeable mutant and wild-type strains of H. pylori.
10. The immune antiserum of claim 9, wherein the IgG causes complement-mediated bacteriolysis of mutant and wild-type α1,6-glucan-expressing H. pylori strains.
Type: Application
Filed: Oct 24, 2016
Publication Date: May 11, 2017
Inventors: Eleonora Altman (Winnipeg), Blair A. Harrison (Nepean), Vandana Chandan (Nepean)
Application Number: 15/332,444
