FUSION PROTEINS HAVING MUTATED IMMUNOGLOBULIN HINGE REGION

A fusion protein having a non-immunoglobulin polypeptide having a cysteine residue proximal to the C terminal thereof, and an immunoglobulin component with a mutated hinge region is provided. The mutation comprises a point mutated site corresponding in position to the position in a native hinge region of the cysteine residue located nearest the cysteine residue of the non-Ig component. The distance from the cysteine residue of the non-immunoglobulin polypeptide and any remaining cysteine residues of the mutated hinge region is sufficient to prevent the formation of a disulphide bond therebetween.

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Description
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 13/275,205, filed 17 Oct. 2011, which is a continuation of U.S. patent application Ser. No. 12/180,455 filed 25 Jul. 2008, which claims the benefit of U.S. provisional patent application No. 60/952,181, filed 26 Jul. 2007. The disclosure of each of the previously referenced patent application(s) and patent(s) is hereby incorporated by reference in its entirety.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is 700171403C2_SEQUENCE_LISTING.txt. The text file is 18 KB, was created on Jun. 4, 2021, and is being submitted electronically via EFS-Web.

TECHNICAL FIELD

This application relates to fusion proteins.

BACKGROUND

Recombinant human proteins corresponding to their natural amino acid sequences have been used for the treatment and diagnosis of a broad range of human diseases since the 1980s. However, most recombinant human proteins do not survive long enough in vivo and are rapidly cleared from circulation. For example, proteins with a molecular mass less than 20 kDa have been reported to be filtered at the level of renal tubules, often leading to a dose-dependent nephrotoxicity. The short in vivo half-life of these proteins compromises their natural biological functions, requiring higher doses or more frequent administration, which in turn impairs patient compliance and increases the burden on health care providers. These clinical demands merit the search and development of therapeutic proteins with longer circulation half-life. In addition to the direct mutations of individual protein structure for achieving longer half-life (e.g. ARANESP™ by Amgen and TNKnase by Genentech), two systemic approaches have been used for the creation of therapeutic proteins with longer half-life. One is “PEGylation”, which refers to chemical cross-linking of polyethylene glycol (PEG) compounds to target proteins. PEG-bound proteins have larger molecular sizes and are more slowly cleared from the circulation. PEGylation has been clinically demonstrated and recognized by the biotech industry as a standard method of extending the half-life of various target proteins. A shortcoming of PEGylation is the significant impairment of the biological activity of target proteins. The altered structure of PEGylated proteins also risks generating an immunogenic response in the human body.

Another systemic approach is the genetic fusion of target therapeutic protein(s) with another human carrier protein to stabilize the target protein in circulation in the form of a fusion protein complex. Two ideal human carrier protein candidates for fusion with therapeutic proteins are human immunoglobulin and albumin. Both immunoglobulin and albumin are very stable and abundant in blood. Fusion proteins comprising a therapeutic protein and either immunoglobulin or albumin would theoretically retain the biological activity of the therapeutic protein, be more stable in circulation than the therapeutic protein alone, and be completely homologous to natural human proteins, minimizing the risk of immunogenic responses [1,2].

One practical strategy with this approach is to genetically fuse a therapeutic protein with an Fc fragment of a human immunoglobulin [1, 3, 4]. Modern bioengineering technology has successfully created fusion proteins consisting of a therapeutic protein, such as cytokines and soluble receptors, and an Fc fragment of immunoglobulin G (IgG) [5-26]. For example, IL-10, an anti-inflammatory and anti-rejection agent, has been fused to the N-terminal of murine Fc.gamma.2a to increase IL-10′s short circulating half-life [9]. In another example, the N-terminal of human IL-2 has been fused to the Fc portion of human IgG 1 or IgG 3 to overcome the short half life of IL-2 and its systemic toxicity [26]. Two fusion proteins comprising an Fc fragment have been successfully developed as biomedicines and approved by FDA for the treatment of rheumatoid arthritis and chronic plaque psoriasis [27, 28, 29].

Human IgG is composed of four polypeptides (two identical copies of light chain and heavy chain) covalently linked by disulfide bonds. The proteolysis of IgG by papain generates two Fab fragments and one Fc fragment. The Fc fragment consists of two polypeptides linked by disulfide bonds. Each polypeptide, from the N-terminal to C-terminal, is composed of a hinge region, a CH2 domain and a CH3 domain. The structure of the Fc fragment is nearly identical across all subtypes of human immunoglobulin. IgG is one of the most abundant proteins in the human blood and makes up 70 to 75% of the total immunoglobulin in human serum. The half-life of IgG in circulation is the longest among all five types of immunoglobulin and may reach 21 days.

Disulfide bonds formed between thiol groups of cysteine residues play an important role in the folding and stability of proteins, usually when proteins are secreted to an extracellular medium. The disulfide bond stabilizes the folded form of a protein in several ways. First, it holds two portions of the protein together, biasing the protein towards the folded state. Second, the disulfide bond may form the nucleus of a hydrophobic core of the folded protein, i.e., local hydrophobic residues may condense around the disulfide bond and onto each other through hydrophobic interactions. Third, and related to the first and second points, by linking two segments of the protein chain and increasing the effective local concentration of protein residues, the effective local concentration of water molecules is lowered. Since water molecules attack amide-amide hydrogen bonds and break up secondary structures, disulfide bonds stabilize secondary structure in their vicinity. For example, researchers have identified several pairs of peptides that are unstructured in isolation, but adopt stable secondary and tertiary structure upon forming a disulfide bond between them. The native form of a protein is usually a single disulfide species, although some proteins may cycle between a few disulfide states as part of their function. In proteins with more than two cysteines, non-native disulfide species, which are almost always unfolded, may be formed.

A flexible junction region of the fusion protein which allows the two ends of the molecule to move independently plays a very important role in retaining each of the two moieties' functions separate and efficient. Therefore, the junction region should act as a linker which combines the two parts together, and as a spacer which allows each of the two parts to form its own biological structure and not interfere with the other part. Furthermore, in order to avoid the induction of immunogenicity, the junction region should be native to the human body and simple in structure [5, 25].

The primary structure of the hinge region of immunoglobulin includes three cysteines, such as cys223, cys229 and cys232 in the case of the human IgG 1 structure used by the present inventors. While the cys229 and cys232 form two interchain disulfide bonds by binding between counterparts of the two chains, the cys223 remains free. Therefore, it is highly possible that this free cysteine may bind with another intrachain or interchain cysteine, to form a non-native disulfide bond in the protein maturation process upon secretion from host cells or during subsequent purification. This non-native disulfide bond may not only alter the structure and conformation of the therapeutic protein, but may also interfere with the biological activity of the therapeutic protein or induce harmful immunogenicity when the fusion protein is administrated into the human body.

Many therapeutic proteins such as erythropoietin (EPO) and granulocyte macrophage colony-stimulating factor (GM-CSF) have a cysteine near their C-terminal. The role of this cysteine in maintaining proper structure and function has yet to be well-defined. The cysteine proximal to the C-terminal may be essential for maintaining proper structure, facilitating correct folding or retaining normal biological activity. The inventors hypothesize that if proteins with a cysteine near its C-terminal are fused to the natural sequence of the hinge region of a Fc fragment, the very limited space between the last cysteine of the C-terminal of the fused protein and the first cysteine of the N-terminal of the Fc fragment (cys223) may lead to the formation of an unexpected disulfide bond between these two cysteines. The formation of the unexpected disulfide bond may alter the structure and/or the folding of the fused protein component as well as alter the flexibility of the hinge region. As a result, normal functions of the fused therapeutic protein in the fusion protein complex may be impaired.

Even if the target therapeutic protein does not contain a cysteine near its C-terminal, another cysteine in its structure may, after three dimensional folding, become sufficiently close to the free cysteine (e.g. cys223) of the hinge region to form a non-natural disulfide bond that may alter the structure and biological activity of the fused target protein. The inventors' hypothesis may partially explain why there has yet to be any clinically-proven success in attempts to create functional fusion proteins with widely-used growth factors such as EPO, G-CSF and GM-CSF, etc.

Previous reports have used various methods to create fusion proteins between a therapeutic protein and an Fc fragment/immunoglobulin molecule. In most of these reports, researchers changed amino acid sequences of the target protein, added a linker peptide between the C-terminal of the target protein and the N-terminal of the hinge region of Fc fragment, or truncated the hinge region of the Fc fragment of the hinge region (resulting in the removal of the free cysteine (e.g. cys223)).

In U.S. Pat. No. 5,908,626, a fusion protein of IFN β with a human immunoglobulin Fc fragment is described which was linked by a synthetic oligopeptide (GGS)2(GGGS)2 [6]. The inventors in that patent believe this linker can “reduce the possibility of generating a new immunogenic epitope (a neoantigen) at what would otherwise be the fusion point of the IFN β and the immunoglobulin Fc fragment”. In U.S. Pat. Nos. 6,797,493, 6,900,292, 7,030,226, 7,226,759, and 7,232,668, the hinge region was replaced by a 16-amino acid peptide linker GS(GGGS)3GS [10, 12, 13, 20, 21]. In addition to the genetic approach, chemical manipulation has also been used to address the problem of non-native disulfide bonds. For example, the inventors in U.S. Patent No. 6,808,902 developed a process for treating an IL-lra-Fc fusion protein with a copper (II) halide in order to prevent or correct a non-native disulfide bond which caused misfolding of that fusion protein [12]. An Fc-EPO fusion protein (rather than the conventional EPO-Fc fusion) has shown poor pharmacokinetics and little EPO efficacy in mice; mutation of four amino acids of the EPO molecule is required to obtain a functional Fc-EPO fusion protein [30].

As mentioned above, the hinge region plays the role of the flexible junction region between the fused therapeutic protein and the Fc fragment (CH2 and CH3). Truncation or significant changes of the hinge region may have undesirable effects on ability of the hinge region to act as flexible junction. The addition of peptide linkers may not only impair the natural conformation of the fusion protein but also greatly increase the risk of immunogenecity by introducing a non-native structure.

The need exists for therapeutic protein/Fc fragment fusion proteins that have a prolonged half-life and/or enhanced activity without increasing the risk of an immunogenic response.

SUMMARY OF THE INVENTION

According to one aspect of the present invention, a fusion protein having a non-immunoglobulin polypeptide having a cysteine residue proximal to the C terminal thereof, and an immunoglobulin component with a mutated hinge region is provided. The mutation comprises a point mutated site corresponding in position to the position in a native hinge region of the cysteine residue located nearest the cysteine residue of the non-Ig component. The distance from the cysteine residue of the non-immunoglobulin polypeptide and any remaining cysteine residues of the mutated hinge region is sufficient to prevent the formation of a disulphide bond therebetween.

According to one aspect of the present invention a fusion protein having a non-immunoglobulin polypeptide and an immunoglobulin component is provided. The immunoglobulin component has a mutated hinge region. The mutation comprises a point mutated site in a hinge region of the immunoglobulin component promixate to the non-immunoglobulin polypeptide. A cysteine residue of the hinge region is substituted by a non-cysteine residue.

According to one aspect of the present invention, a fusion protein having a non-immunoglobulin polypeptide directly linked to a human immunoglobulin component is provided. The fusion protein has a prolonged half-life in vivo in comparison to naturally occurring or recombinant native non-immunoglobulin polypeptide.

According to one aspect of the invention, multimeric proteins comprising a plurality of the fusion proteins according to the foregoing aspects of the invention are provided.

According to one aspect of the invention, methods of producing fusion proteins according to the foregoing aspects of the invention are provided. The methods include the step of culturing a cell line transfected with a DNA molecule that encodes the sequence of the fusion protein and purifying the encoded protein.

According to one aspect of the invention, methods of stimulating white blood cell production in a mammal are provided, wherein the methods include the step of administering to the mammal a fusion protein according to the foregoing aspects of the invention.

According to one aspect of the invention, pharmaceutical compositions including a fusion protein according to the foregoing aspects of the invention and a pharmaceutically acceptable carrier, adjuvant or diluent are provided.

According to one aspect of the invention, methods of stimulating white blood cell production in a mammal are provided, wherein the methods include the step of administering to the mammal a pharmaceutical composition according to foregoing aspects of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

In drawings intended to illustrate various embodiments of the invention but which are not intended to be constructed in a limiting manner.

FIG. 1 is a set of schematic diagrams illustrating the strategy for generating point mutations and the amplification of the mutated whole gene encoding a Fc fusion protein simultaneously by overlapping PCR. FIG. 1A illustrates a base-pair mutation was introduced into primers P2 and P3. The overlapping fragments of non-Ig and Fc with the desired mutation were amplified by p1/p3 and p2/p4 respectively. FIG. 1B illustrates the mixed fragments from A served as a template. The whole molecule with the desired mutation was amplified by p1/p4. FIG. 1C illustrates the resulting whole molecule with the desired mutation. X represents the non-Ig moiety of fusion protein.

FIG. 2A is a schematic diagram showing the general structure of the DNA molecule encoding the recombinant human EPO-FcG fusion protein (rHuEPO-FcG) in which the first cysteine from the N-terminal of the hinge region (cys223) is substituted by glycine and used as the mutant hinge region for the construction of an EPO-Fc fusion protein. This mutant hinge region-containing Fc fragment is referred to as FcG, and the Fc fragment containing the hinge region with the native cysteine at the sixth residue from its N-terminal as FcC respectively.

FIG. 2B is a sequence listing showing the nucleotide sequence [SEQ ID NO:1] and the deduced amino acid (aa) sequence [SEQ ID NO:2] of rHuEPO-FcG protein. The total length of DNA is 1281 bp. The 426 amino acids in the deduced protein sequence include 27 aa for the signal peptide and 399 aa for the complete rHuEPO-FcG protein. The complete rHuEPO-FcG protein consists of human EPO domain (166 aa), hinge region (16 aa, underlined), and CH2 and CH3 domains (217 aa) of the Fc fragment of human IgG1. The calculated molecular weight of the polypeptide of the mature rHuEPO-FcG fusion protein is 44.6 kDa, composed of 18.5 kDa (41.4%) of EPO fragment and 26.1 kDa (58.6%) of IgG 1 Fc fragment. A homodimer is formed by two disulfide bonds via the two cysteine residues (boxed) within the hinge region. At residue 172 of the mature fusion protein (i.e. the 6th amino acid of hinge region) the native cysteine residue has been substituted by glycine (bold).

FIG. 3A is a schematic diagram showing the general structure of the DNA molecule encoding the wild type human EPO-FcC fusion protein (rHuEPO-FcC) in which the first cysteine from the N-terminal of the hinge region (cys223) is maintained.

FIG. 3B is a sequence listing showing the nucleotide sequence [SEQ ID NO:3] and the deduced amino acid (aa) sequence [SEQ ID NO:4] of a wild type rHuEPO-FcC protein. The sequence particulars are the same as shown in FIG. 2B except that the native, wild type cysteine residue is maintained at residue 172 of the mature fusion protein (i.e. the 6th amino acid of the hinge region).

FIG. 4A is a schematic diagram showing the general structure of the DNA molecule encoding the fusion protein between native GM-CSF molecule and the FcG fragment (HuGMCSF-FcG).

FIG. 4B is a sequence listing showing the nucleotide sequence [SEQ ID NO:5] and the deduced amino acid (aa) sequence [SEQ ID NO:6] of rHuGMCSF-FcG fusion protein. The total length of DNA is 1131 bp. The 377 amino acids in the deduced protein sequence include 17 aa for the signal peptide and 360 aa for the complete HuGMCSF-FcG fusion protein. The complete rHuGMCSF-FcG fusion protein consists of complete GM-CSF molecule (127 aa), mutant hinge fragment (16 aa, underlined), and CH2 and CH3 domains (217 aa) of the Fc fragment of human IgG 1. The calculated molecular weight of mature rHuGMCSF-FcG fusion protein is 40.6 kDa, composed of 14.5 kDa (35.7%) of GM-CSF fragment and 26.1 kDa (64.3%) of IgG 1 Fc fragment. A homodimer is formed by two disulfide bonds via the two cysteine residues (boxed) within the hinge region. At residue 150 of the fusion protein (i.e. the 6th amino acid of hinge region) the native cysteine residue has been substituted by glycine (bold).

FIG. 5 is an image showing the sizes of the dimeric form of pure rHuEPO-FcG protein in non-reduced condition (lane A) and monomeric form of pure rHuEPO-FcG protein in reduced condition (lane B) by SDS-PAGE analysis. The purified rHuEPO-Fc protein from the supernatants of the cultured CHO cell-line expressing rHuEPO-FcG exists mainly as the dimeric form and has a molecular weight of about 180 kDa on 8% bis-tris gel in non-reduced condition. In reduced condition (100 mM dithiothreitol (DTT)) to break disulfide bonds, the dimer is separated into two identical monomeric units with a molecular weight of 75 kDa.

FIGS. 6A and 6B are graphs showing the dose-dependent increase of hemoglobin (Hb) levels in normal mice treated three times per week with a subcutaneous injection (s.c.) of rHuEPO-FcG or rHuEPO. Each point represents the mean Hb level of the group (6 mice). Day 0 levels represent the Hb levels before treatment. FIG. 6A shows results for mice treated with rHuEPO-FcG. FIG. 6B shows results for mice treated with native rHuEPO.

FIG. 7A and 7B are graphs showing the dose-dependent increase of hemoglobin (Hb) levels in normal mice treated with once per week s.c. of rHuEPO-FcG or rHuEPO. Each point represents the mean Hb level of the group (6 mice). Day 0 levels represent the Hb levels before treatment. FIG. 7A shows results for mice treated with rHuEPO-FcG. FIG. 7B shows results for mice treated with native rHuEPO.

FIG. 8A and 8B are graphs showing the increase of hemoglobin (Hb) levels in normal mice treated with intravenously injection (i.v.) of 12.5 μg/kg of rHuEPO-FcG or rHuEPO. Each point represents the mean Hb level of the group (6 mice). Day 0 levels represent the Hb levels before treatment. FIG. 8A shows results for mice with treatment once a week. FIG. 8B shows results for mice with treatment 3 times a week.

FIG. 9 is a graph showing the dose-dependent increase of hemoglobin (Hb) levels in ⅚ nephrectomized rats treated with once per week s.c. of rHuEPO-FcG, rHuEPO or darbepoetin-alfa (abbreviated Darbe.). Each point represents the mean Hb level of the group. Normal controls were normal rats with injection of carrier solution. Model controls were the ⅚ nephrectomized rats with injection of carrier solution. Week 0 levels represent the Hb levels before treatment. *: week(s) post treatment.

FIG. 10 is a graph showing the dose-dependent increase of hemoglobin (Hb) levels in ⅚ nephrectomized rats treated once every two weeks s.c. with rHuEPO-FcG, rHuEPO or darbepoetin-alfa (abbreviated Darbe.). Each point represents the mean Hb level of the group. Normal controls were normal rats with injection of carrier solution. Model controls were the ⅚ nephrectomized rats with injection of carrier solution. Week 0 levels represent the Hb levels before treatment. *: week(s) post treatment.

FIG. 11 is a graph showing the dose-dependent increase of hemoglobin (Hb) levels in ⅚ nephrectomized rats treated once every two weeks i.v. with 62.5 μg/kg of rHuEPO-FcG, or darbepoetin-alfa (abbreviated Darbe.). Each point represents the mean Hb level of the group. Normal controls were normal rats with injection of carrier solution. Model controls were the ⅚ nephrectomized rats with injection of carrier solution. Week 0 levels represent the Hb levels before treatment. *: week(s) post treatment.

FIGS. 12A to 12C are graphs comparing the potency of rHuEPO-FcG, rHuEPO and darbepoetin-alfa in stimulating the colony formation of CFU-E and BFU-E in ⅚ nephrectomized rats treated with different doses and schedules. rHuEPO-FcG and darbepoietin-alpha (abbreviated Darbe.) treatment showed similar dose-dependent potencies for stimulating the CFU-E and BFU-E colony formation, while rHuEPO was less potent. FIG. 12A shows results for s.c. once every week. FIG. 12B shows results for s.c. once every 2 weeks. FIG. 12C shows i.v. once every two weeks.

FIG. 13 is a graph showing the serum levels of rHuEPO-FcG and rHuEPO after the intravenous injection of 5 μg/kg of rHuEPO-FcG or rHuEPO to Rhesus monkeys (mean levels of 5 monkeys).

FIG. 14 is a graph showing the dose-dependent increase of hemoglobin (Hb) levels in normal mice treated three times per week with subcutaneous injection (s.c.) of rHuEPO-FcG, rHuEPO-FcC and rHuEPO. Each point represents the mean Hb level of the group (8). Normal control was normal mice with injection of carrier solution. Day 0 levels represent the Hb levels before treatment.

FIG. 15 is a graph showing the dose-dependent increase of hemoglobin (Hb) levels in normal mice treated once per week with subcutaneous injection (s.c.) of rHuEPO-FcG, rHuEPO-FcC and rHuEPO. Each point represents the mean Hb level of the group (8). Normal control was normal mice with injection of carrier solution. Day 0 levels represent the Hb levels before treatment.

FIG. 16 is a graph comparing the growth of white blood cells (WBC) in dogs with experimental neutropenia by rHuGMCSF-FcG or by rHuGMCSF. 6° Co y-ray irradiated dogs were treated s.c. with 10 μg/kg of rHuGMCSF-FcG every other day, 20 μg/kg of rHuGMCSF-FcG every other day, or 20 μg/kg of rHuGMCSF every day. Day −1 and day 1 represent the day before irradiation and the next day after irradiation respectively. Treatment started from day 1 and lasted for 10 days. Clinical observation and examination of WBC counts lasted for 28 days. Each point represents the mean WBC counts of the group. Model controls were the irradiated dogs with injection of carrier solution only.

 DETAILED DESCRIPTION OF THE INVENTION

Throughout the following description specific details are set forth in order to provide a more thorough understanding of the invention. However, the invention may be practiced without these particulars. In other instances, well known elements have not been shown or described in detail to avoid unnecessarily obscuring the present invention. Accordingly, the specification and drawings are to be regarded in an illustrative, rather than a restrictive sense.

This invention relates to recombinant human fusion proteins combining a target protein or polypeptide, such as a non-immunoglobulin polypeptide, with a Fc fragment or immunoglobulin molecule. The Fc fragment or Ig molecule includes a mutant hinge region wherein the first cysteine from the N-terminal of the hinge region (e.g. in human IgG 1, the sixth amino acid, cys223) is replaced by a non-cysteine residue, such as a non-charged, non-polar amino acid (neutral amino acid). The result is a mutant hinge region which maintains the natural length and flexibility of the hinge region without the free cysteine that may lead to the formation of a non-natural disulfide bond with a cysteine in the non-immunoglobulin polypeptide. The mutant hinge region may comprise the whole or part of the human Fc fragment, or the whole or part of a human immunoglobulin molecule.

When any non-immunoglobulin polypeptide is directly fused to the hinge region of the Fc fragment or Ig molecule to form a protein-Fc or protein-Ig fusion protein, respectively, it is believed the mutant hinge region lacking the N-terminal free cysteine allows the fused target polypeptide to maintain its structure, folding and biological functions. In particular, it is believed that any cysteine residues proximal to the C terminal of the target non-immunoglobulin polypeptide are thus prevented from forming any unexpected disulphide bonds with the N-terminal free cysteine found in the native hinge region. Cysteine residues “proximal” to the C terminal of the non-immunoglobulin polypeptide include those proximal with reference to position along the amino acid chain and as well to those proximal as result of three-dimensional folding of the non-immunoglobulin polypeptide. The fusion proteins created with this mutant hinge region have near 100% sequence identity to natural sequences of both the target protein and hinge region, and therefore possess minimum immunogenecity risks.

The first cysteine from the N-terminal of the hinge region of human Fc fragment/immunoglobulin (e.g. the sixth amino acid, cys223, in human IgG 1) may be substituted with any non-charged, non-polar amino acid (neutral amino acid). In the example disclosed herein, glycine was used to replace the free cysteine. A person skilled in the art would appreciate that other amino acids could also replace the free cysteine.

The mutant hinge region that is formed by substituting the free cysteine near its N-terminal as part of the Fc fragment or Ig molecule provides a method or platform for generically producing fusion proteins between any non-immunoglobulin polypeptide and Fc/Ig to prevent non-naturally occurring disulfide bonds, and thus retain the biological functions of the fused target polypeptide.

Several methods can be used to make the desired point mutation. One method, described in Example 1 of this invention, adopts overlapping PCR to amplify the whole nucleic acid sequence of the fusion protein. With specifically-designed oligo primers, the desired point-mutation can be introduced into the resulting nucleic acid sequence following gene amplification. Other methods, such as the Quick-Change™ mutagenesis method from Invitrogen or artificial gene synthesis can also be used to produce the point mutation. A person skilled in the art would appreciate that any number of different methods could be used to substitute the free cysteine of the hinge region (e.g. cys223).

The fusion protein created by using the mutant hinge region according to an embodiment of the present invention comprises a non-Ig moiety linked to an Fc fragment of IgG expressed by the formula “X-hinge region-CH2—CH3”, wherein X represents the non-Ig moiety, and CH2 and CH3 represent two heavy chain domains of the Fc fragment of IgG.

The hinge region refers to the region between the CH1 and CH2 heavy chain domains that contains the interchain disulfide bonds. Flexibility in this region allows the molecules on both sides of hinge region to move independently. The heavy chains are also glycosylated in this region, which helps protect this relatively exposed area against degradation. In one embodiment, the non-Ig moiety of the fusion protein links to the hinge region directly, i.e. the C-terminal of the non-Ig moiety is directly fused to the N-terminal of hinge region. The first cysteine (e.g. cys223) from the N-terminal of the hinge region may be substituted by a non-charged, non-polar amino acid, such as glycine. In some embodiments, a synthetic linker, such as (G4S)3 or G4SG5S, may be inserted between the non-Ig moiety and Fc fragment to ensure each part folds properly. In other embodiments, one or more of the amino acid residues upstream of the first cysteine (e.g. cys223) site may be removed.

The non-immunoglobulin polypeptide may be, but is not limited to, any peptide or polypeptide sequence with human or non-human origin, having complete or non-complete amino acid sequences corresponding to any defined human and non-human proteins, exhibiting biological functions or non-biological functions, made artificially or obtained naturally. The non-immunoglobulin polypeptide may also be a variant of any proteins defined or non-defined before. These variants include but are not limited to polypeptide sequences modified from a native protein sequence but still partially or completely retaining its biological functions. Modifications include but are not limited to substitution, addition, insertion, deletion, or rearrangement of the amino acids of the native polypeptide sequences.

The non-immunoglobulin polypeptide may, for example, be a cytokine. “Cytokine” is used herein to describe proteins, analogs thereof, and fragments thereof which are produced by and excreted from a cell, and which elicit the biological response by binding with corresponding receptors. Cytokines include but are not limited to hematopoietic factors such as EPO, GM-CSF and granulocyte colony stimulating factor (G-CSF), interferons such as IFN α, IFN β and IFN γ, interleukins such as IL-2, IL-4, IL-5, IL-6, IL- 7, IL-10, IL-11, IL-13, IL-14, IL-15, IL-16 and IL-18, tumor necrosis factors such as TNF α, and lymphokines such as lymphotoxin.

The non-immunoglobulin polypeptide may also be a ligand-binding protein that may block a receptor-ligand interaction at the cell surface, or neutralize the biological activity of another molecule in the body fluids. Ligand-binding proteins include but are not limited to CDs molecules, CTLA-4, TNF receptors, and interleukin receptors.

The non-immunoglobulin polypeptide may also be a hormone, a neurotrophin, a neutrophin receptor (e.g. Trk A), a body-weight regulator, a serum protein, a clotting factor, a protease, an extracellular matrix component, an angiogenic factor, an anti-angiogenic factor, an immunoglobulin receptor (e.g. IgG receptor), a blood factor (e.g. Factor VIII, Factor IX, Factor X), a cancer antigen (e.g. PSA, PSMA), a statin (e.g. endostatin, angiostatin) a therapeutic peptide or a growth-factor (e.g. Flt-3).

The non-immunoglobulin polypeptide may also be a non-human or non-mammalian protein, or even a protein toxin. Examples include gp120, HIV transactivators, surface proteins from other viruses such as HBV, HCV and RSV, and parasitic surface proteins such as malarial antigens.

A recombinant vector with the nucleic acid sequence encoding the Fc fragment containing a mutant hinge region may be constructed. This vector, which possesses all the elements needed for its propagation, selection, and screening in either prokaryotic cells (such as E. coli) or eukaryotic cells (such as CHO cells), can serve as a platform to express Fc fusion proteins described in this invention. By using this platform, the nucleic acid sequence encoding the non-Ig moiety of the fusion protein is conveniently inserted in-frame into the vector at the 5′-end of nucleic acid sequence encoding the mutated Fc moiety by molecular cloning techniques.

As a specific example, a novel fusion protein having enhanced erythropoietic properties was produced according to the present invention. The fusion protein, referred to herein as rHuEPO-FcG, comprises a human EPO molecule genetically linked to an immunoglobulin Fc fragment containing a mutant hinge region of the present invention. The nucleic acid sequence of the rHuEPO-FcG fusion protein of the present invention is shown in SEQ ID No: 1, and the corresponding deduced amino acid sequence is shown in SEQ ID No: 2. As discussed further below, the fusion protein may be in the form of a dimer comprising two identical polypeptide subunits. Each polypeptide subunit, from the N-terminal to C-terminal, includes the polypeptide sequence of the human EPO molecule, and the polypeptide sequence of the hinge region, CH2 domain and CH3 domains of the Fc fragment of human immunoglobulin IgG 1 as shown in FIG. 2A. The two polypeptide subunits are joined by disulfide bonds between the respective hinge regions to form the dimer structure. The dimer has the same general shape as an IgG molecule and exhibits better stability than free EPO molecules as demonstrated in the examples below.

As will be apparent to a person skilled in the art, the hinge region of an intact immunoglobulin provides the protein sufficient flexibility for effective antigen-antibody binding. Similarly, in the present invention, the hinge region in which the free cysteine (e.g. cys223) is substituted by glycine is included in the design of the rHuEPO-FcG fusion protein to maintain its flexibility, particularly when the fusion protein is in the dimer form. As described below, this likely allows the normal binding of the EPO portion of the rHuEPO-FcG fusion protein to EPO receptors to effect the biological functions of EPO. It is believed that the dimer form of the rHuEPO-FcG fusion protein, by providing two EPO molecules, is capable of inducing optimal activation of EPO receptors (for example, by facilitating receptor cross-linking).

As demonstrated in the examples set forth below, the rHuEPO-FcG fusion protein has been successfully synthesized using recombinant DNA techniques. The fusion protein has been shown in mice, rat and primate studies to exhibit a prolonged in vivo half-life and enhanced erythropoietic properties in comparison to naturally occurring or recombinant native human EPO. The rHuEPO-FcG fusion protein containing the mutant hinge region exhibits normal or even enhanced erythropoietic functions in normal animals and animals with experimental anemia. The half-life of this fusion protein in circulation in primate studies reached 37 hours in comparison to 8 hours for native human erythropoietin and 24 hours for ARANESP from Amgen. As used in this patent application, the terms “native human erythropoietin” and “native human EPO” mean EPO having an identical and complete amino acid sequence of the wild type EPO molecule. As will be appreciated by a person skilled in the art, native human EPO may be naturally occurring or recombinantly produced (e.g. rHuEPO alpha). The term “native human EPO” does not include rHuEPO analogs, such as darbepoetin alpha where the EPO structure has been significantly modified, such as by hyperglycosylation.

The nucleic acid sequence of the rHuEPO-FcG fusion protein of the present invention is shown in FIG. 2B. The complete rHuEPO-FcG fusion protein is 399 amino acids in length. As shown in FIG. 2B, the complete rHuEPO-FcG fusion protein consists of the EPO domain (166 amino acids), the hinge region (16 amino acids, underlined) and the CH2 and CH3 domains (217 amino acids). A signal or leader peptide sequence consisting of 27 amino acids is also shown in FIG. 2B. The signal peptide is cleaved during synthesis of rHuEPO-FcG.

As shown best in FIG. 2B, the EPO domain has a cysteine residue near its C-terminal (amino acid number 161). The mutant hinge region includes 2 cysteine residues, at amino acid numbers 178 and 181 which are boxed in FIG. 2B. The hinge region cysteine residues form the disulphide bonds between the polypeptide subunits of the homodimer as discussed above. The naturally occurring hinge region of a human IgG 1 fragment also has a cysteine at residue number 6 of the hinge region portion (measured from the N-terminal). According to an embodiment of the present invention, the cysteine residue 6 of the hinge portion has been substituted by a non-cysteine residue. In particular, in the embodiment of FIG. 2B, the cysteine has been substituted by glycine (at amino acid residue 172 of rHuEPO-FcG, which corresponds to residue 6 of the hinge region), causing the sequence difference as compared to the protein of FIGS. 3A and 3B. As will be apparent to a person skilled in the art, other non-cysteine residues could also be substituted for cysteine at this location to avoid formation of a disulfide bond.

As a result of the amino acid substitution at residue 172, the first cysteine residue of the hinge region (at residue 178) is spaced 17 amino acids from the above-described cysteine residue of the EPO domain (at residue 161). The inventors believe that the minimum spacing between the cysteine residue 161 of the EPO domain and the first cysteine residue of the hinge region should be at least 12 amino acids to enable successful assembly and/or EPO receptor binding of a homodimer of rHuEPO-FcG. That is, if residue 172 is a cysteine residue, an undesirable disulfide bond may potentially be formed, such as between cysteine residues 161 and 172. This may alter the three dimensional structure of the EPO molecule, resulting in the impairment and/or the loss of the biological functions of EPO.

In one embodiment of the invention, the EPO domain is linked directly to the Fc fragment portion of the fusion protein. By avoiding an external linker peptide, the preferred three dimensional structure of the rHuEPO-FcG fusion protein is maintained and the risk of triggering an undesirable immunogenic response is minimized. The hinge region of the Fc fragment is preferably at least 9 amino acids in length and is preferably in the range of about 10 to 20 amino acids in length.

As another specific example, a fusion protein combining human GM-CSF and the mutated Fc fragment was also produced genetically (rHuGMCSF-FcG), as illustrated in FIG. 4A. The nucleic acid sequence of the rHuGMCSF-FcG fusion protein of the present invention is shown in SEQ ID No: 5 and FIG. 4B. The corresponding deduced amino acid sequence is shown in SEQ ID No: 6 and FIG. 4B. In vivo experiments in animals with experimental neutropenia demonstrate that rHuGMCSF-FcG exhibits enhanced biological functions in terms of stimulating the growth of white blood cells (WBC) as compared to rHuGMCSF.

Accordingly, two fusion proteins formed by direct linking of the target proteins, human EPO and GM-CSF, to the mutant hinge region in which the free cysteine (e.g. the sixth amino acid, cys223, in human IgG 1) was substituted by glycine, showed at least full biological functions of the fused target proteins, as compared to their natural molecules. These results strongly suggest that the mutant hinge region of the present invention allows the direct fusion of a target protein to an Fc fragment/Ig molecule while retaining biological functions of the fused target protein. The resulting fusion protein of target protein-Fc/Ig complex, in addition to retaining natural biologic functions, exhibits significantly prolonged half-life in vivo.

In a further embodiment, the mutant hinge region without the free cysteine (e.g. the sixth amino acid, cys23, in human IgG 1) could be used as a standard platform for generating fusion proteins that have longer circulation half-life and/or exhibit full or enhanced biological functions compared to the target protein. Unlike PEGylation, an advantage of making fusion proteins of the present invented is that the biological activity of the target protein will not be impaired and the potential immunogenic responses are minimized since the fusion protein has almost 100% sequence identity to natural human proteins (i.e., only one amino acid is different).

Examples

The following examples will further illustrate the invention in greater detail although it will be appreciated that the invention is not limited to the specific examples.

1. Generation and Amplification of Mutated Nucleic Acid Sequences Encoding the Fusion Proteins rHuEPO-FcG and rHuGMCSF-FcG

Full length DNA molecules encoding the amino-acid sequence of the polypeptide of rHuEPO-FcG, rHuEPI-FcC (wild type) and rHuGMCSF-FcG were generated by overlapping PCR using the following oligo primers (QIAGEN Inc., US), respectively:

EF5: [SEQ ID NO: 7] 5′-ccggaattcgccaccatgggggtgcacgaatgtcctgcct-3′ EF3: [SEQ ID NO: 8] 5′-ttttccttttgcggccgcttatttacccggagacagggagag-3′ EFL5: [SEQ ID NO : 9] 5′-aggcctgcaggacaggggacagagttgagcccaaatctggtgaca-3′ EFL3: [SEQ ID NO: 10] 5′-tgtcaccagatttgggctcaactctgtcccctgtcctgcaggcct-3′ EFL5w: [SEQ ID NO: 11] 5′-aggcctgcaggacaggggacagagttgagcccaaatcttgtgaca-3′ EFL3w: [SEQ ID NO: 12] 5′-tgtcacaagatttgggctcaactctgtcccctgtcctgcaggcct-3′ GF5: [SEQ ID NO: 13] 5′-actgaattcgccaccatgtggctgcagagcctgctgctcttgggcact gtggcctgc-3′ GF3: [SEQ ID NO: 14] 5′-ttttccttttgcggccgcttatttacccggagacagggagag-3′ GFL5: [SEQ ID NO: 15] 5′-gactgctgggagccagtccaggaggttgagcccaaatctggtgacaaa ac-3′ GFL3: [SEQ ID NO: 16] 5′-gttttgtcaccagatttgggctcaacctcctggactggctcccagcag tc-3′

An EcoR I site was introduced in EF5 and GF5, and a Not I site was introduced in EF3 and GF3. For optimal expression of the proteins in mammalian cells, the Kozak sequence (GCCACCATGG) was also introduced in EF5 and GF5. The pairs EFL5/EFL3 and EFL3w/EFL5w are complementary sequences consisting of the 3′-terminal DNA sequence of EPO (23 bp) and the 5′-terminal DNA sequence of mutated and wild IgG 1 hinge (22 bp), respectively. The pair of GFL5/GFL3 are complementary sequences consisting of the 3′-terminal DNA sequence of GM-CSF (24 bp) and the 5′-terminal DNA sequence of mutated IgG 1 hinge (26 bp).

A. Generation of Wild and Mutated Sequences of rHuEPO-FcG

First, an EPO DNA fragment of 0.6 kb was amplified by PCR (Platinum Taq DNA Polymerase High Fidelity) with primers EF5 and EFL3 or EFL3w from plasmid p9E containing the full length of human EPO cDNA, mutated and wild Fc fragment of 0.7 kb with primers EF3/EFL5, and EF3/EFL5w from plasmid pD containing the full length of human IgG1 cDNA sequence, respectively (p9E and pD are from the inventors' own lab). The two fragments were then purified and mixed in equal amount. Using the mix as a template, the full length mutated and wild rHuEPO-FcG DNA of 1.3 kb was amplified by primers EF5 and EF3, respectively.

B. Generation of Mutated Sequence of rHuGMCSF-FcG

First, a GM-CSF DNA fragment of 0.4 kb was amplified by PCR (Platinum Taq DNA Polymerase High Fidelity) with primers GF5 and GFL3 from plasmid pSS-GM containing the full length of human GMCSF cDNA, and a mutated Fc fragment of 0.7 kb was amplified with primers GF3/GFL5 from plasmid pD containing the full length of human IgG1 cDNA sequence (pSS-GM and pD are from the inventors' own lab). The two fragments were then purified and mixed in equal amount. Using the mix as a template, the full length of mutated rHuGMCSF-FcG DNA of 1.1 kb was amplified by primers GF5 and GF3.

This method is generally illustrated in FIGS. 1A-1C.

2. Construction of the Recombinant Plasmids

Recombinant plasmids pCdEpo-FcG, pCdEpo-FcC and pCdGMCSF-FcG encoding the fusion protein of rHuEPO-FcG , rHuEPO-FcC and rHuGMCSF-FcG, respectively, were constructed by cloning the amplified nucleic acid sequences from Example 1 into expression vector pCD1.

The purified three fragments were digested by EocR I and Not I (New England Biolab Inc., USA) and then cloned into EcoR I/Not I-digested mammalian expression vector pCD1 (FIG. 2A). The resulting recombinant vectors were named pCdEpo-FcG, pCdEpo-FcC and pCdGMCSF-FcG. The inserted nucleic acid sequences encoding the amino-acid sequence of the rHuEPO-FcG, rHuEPO-FcC and rHuGMCSF-FcG were confirmed by DNA sequencing.

3. Establishment of rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG Expression Cell Lines

Chinese hamster ovary (CHO) cells with dihydrofolate reductase (dhfr) deficiency (CHO/dhfr, ATCC No. CRL-9096), which have been approved by the FDA for biological substance production, were used as host cells for recombinant expression of rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG.

The CHO-dhfr− cells were transfected with the recombinant vectors pCdEpo-FcG, pCdEpo-FcC and pCdGMCSF-FcG using Lipofectamine (Gibco, Cat. No:18292-037, USA). The supernatants from the culture of selected clones were assayed by ELISA (Roche, Cat. No:1-693 417 and Cat. No: HSGMO, Canada) for EPO and GM-CSF activity respectively. Positive clones were further screened under increasing methotrexate (MTX) pressures. Cell lines with highest protein expression were selected, and gradually adapted to serum-free media (CD CHO Medium, Gibco, and Cat. No:10743-029, USA). These selected CHO cell lines were used for the production of rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG, respectively.

4. Purification of rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG Proteins

rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG protein molecules contained in the supernatants collected from the serum-free media culturing the selected CHO cells were isolated at first by Protein A affinity chromatography (Amersham, Cat. No:17-0402-01, Canada). The isolated proteins were further purified by gel filtration in HiLoad 16/60 Superdex 200 pg columns (Amersham, Cat. No:17-1069-01, Canada). The purity of the rHuEPO-FcG , rHuEPO-FcC, and rHuGMCSF-FcG proteins was more than 98% as determined by electrophoresis.

5. Determination of the Sizes of the Purified rHuEPO-FcG Protein

First, SDS-PAGE was carried out to determine the sizes of the purified rHuEPO-FcG, rHuEPO-FcC, and rHuGMCSF-FcG proteins. (FIG. 5). A single band with molecular weight of about 180 kDa for rHuEPO-FcG and rHuEPO-FcC, and 140 kDa for rHuGMCSF-FcG was seen on an 8% Bis-Tris gel under non-reducing conditions, which measures the overall size of the protein with the existence of disulfide bonds. This indicated that most of these recombinant protein molecules were produced in their dimeric form, as expected from the design of the fusion protein. When SDS-PAGE analysis was conducted under reducing conditions (100 mM dithiothreitol (DTT)) to break the disulfide bonds, only single bands with molecular weight of 75 kDa and 60 kDa were identified, consistent with the estimated molecular weight of single polypeptide chains of HuEPO-hinge region-CH2—CH3 and HuGMCSF-hinge region-CH2—CH3, respectively.

The molecular weight of the purified rHuEPO-FcG fusion protein with glycosylation was determined by mass spectrometry (MALDI-TOF-MS) to be 111099 daltons (111.1 kDa). In this assay, only a single peak of protein was observed, indicating that the purified rHuEPO-FcG protein was nearly 100% pure. The 15 amino acids of the N-terminal of the pure rHuEPO-FcG protein were determined by protein sequence analysis as: APPRLICDSRVLERY. This was consistent with the sequence of the first 15 amino acids of the native human EPO polypeptide, and confirms that the purified rHuEPO-FcG G protein does have the correct and complete EPO molecule sequence as predicted by the DNA sequence encoding the amino acid sequences of the rHuEPO-FcG G fusion protein.

6. Enhanced Erythropoietic Activities of rHuEPO-FcG in Normal Mice

In vivo experiments in mice were conducted to confirm the retention of erythropoietic activity of the rHuEPO-FcG protein and to determine its efficacy compared to rHuEPO and darbepoetin-alpha. For comparison purposes, the doses of EPO used in the described animal experiments of the invention, namely rHuEPO-FcG, rHuEPO (i.e., native human EPO) and darbepoetin-alpha, were compared according to the amount of EPO molecule portion alone. In respect of rHuEPO-FcG protein, the EPO portion contributes to 41.4% of the total rHuEPO-FcG molecular weight as calculated by the ratio of the weight of amino acids of EPO to weight of the total amino acids of the whole rHuEPO-FcG molecule (166 of 399 amino acids). The EPO amount for rHuEPO-FcG was thus determined to be 41.4% of the total amount of rHuEPO-FcG protein.

rHuEPO-FcG (stock concentration: 0.5 mg/ml, purity of 98.6%) and native human rHuEPO (i.e. with natural human EPO structure) (6000 IU/0.5 ml, manufactured by Kirin Brewery Co., Japan) were diluted in carrier solution (2.5 mg/ml of human serum albumin, 5.8 mg/ml of sodium citrate, 0.06 mg/ml of citric acid and 5.8 mg/ml of sodium chloride, pH 5.5-5.6). The dose of rHuEPO was calculated according to its activity/amount ratio. BALB/c mice (6 to 8 weeks old, weighing 18-22 g, equal numbers of male and female, purchased from Experiment Animal Center, AMMS, China) were grouped randomly with 6 in each group. Each group of mice was treated with one combination of one dose (0.1, 0.5, 2.5, 12.5, 62.5 μg/kg), one injection route (i.v. through the tail vein or s.c.) and one injection schedule (three times per week or once per week). The control group of mice was injected with an equal volume of carrier solution. The treatment lasted for 3 weeks and the total observation time was 5 weeks. Peripheral blood samples (tail vein) were taken before treatment, on the 4th day and 7th day of every week for 5 weeks. Hemoglobin (Hb) was measured as the index by absorptiometry. Mean±SD was calculated from the data of each group and a t test was conducted among different groups.

The administration of EPO three times per week to mice, provided that the EPOs have normal erythropoietic activity, would induce saturated stimulation of erythropoiesis. As shown in FIGS. 6A and 6B, both groups treated 3 times per week s.c. had significant elevation of Hb levels even at the dose of 2.5 μg/kg. This experiment demonstrated that rHuEPO-FcG exhibited an in vivo erythropoietic activity as effective as rHuEPO. The elevation of Hb levels in the treated group was dose-dependent. However, saturated elevation of the Hb levels was induced in mice at the dose of 12.5 μg/kg of rHuEPO-FcG , whereas the similar saturated elevation of the Hb levels was only achieved at the dose of 62.5 μg/kg of rHuEPO. The elevation of Hb levels induced by 2.5 μg/kg of rHuEPO-FcG was also greater than that by 2.5 μg/kg of rHuEPO. These results suggest more potent erythropoietic stimulation by rHuEPO-FcG compared to rHuEPO.

The erythropoietic potency of rHuEPO-FcG was further explored by reducing the injection times to once per week subcutaneously. As shown in FIGS. 7A and 7B, the rHuEPO-FcG-treated groups showed dose-dependent elevation of Hb levels at the doses of 12.5, or 62.5 μg/kg. Both doses of 12.5 and 62.5 μg/kg of rHuEPO also induced the elevation of Hb levels to a similar extent, which was much lower than that by 62.5 μg/kg of rHuEPO-FcG . This strongly indicates that rHuEPO-FcG has enhanced erythropoietic activity in vivo, presumably due to either the prolonged half-life of the rHuEPO-FcG in vivo or improved EPO receptor binding/activation by the dimer EPO molecules in the rHuEPO-FcG protein, or by the combined effects of both.

When the same doses (12.5 μg/kg) of rHuEPO-FcG or rHuEPO were administrated intravenously either three times per week or once per week, elevation of the Hb levels was observed for all the treated groups (FIGS. 8A and 8B). However, i.v. administration once per week of rHuEPO-FcG induced greater, more persistent elevation of the Hb levels, which continued longer after the treatment was over. This data provides further support for the enhanced erythropoietic properties of the rHuEPO-FcG protein in comparison with rHuEPO having the structure of naturally occurring EPO protein.

7. Enhanced Erythropoietic Activities of rHuEPO-FcG in ⅚ Nephrectomized Rats

Experiments in normal mice proved the enhanced erythropoietic activities of rHuEPO-FcG in vivo. To further observe the efficacy of rHuEPO-FcG in stimulating erythropoiesis, pharmacodynamic studies were conducted in rats with experimental renal anemia induced by ⅚ nephrectomy. The efficacy of rHuEPO-FcG was compared with those of rHuEPO and darbepoetin-alpha (60 μg/ml, lot. No. N079, manufactured by Kirin Brewery Co., Japan).

Wistar rats (male and female in equal number, weighing 160-180 g, purchased from Vitalriver Experiment Animal Inc., Beijing, China. Licence No. SCXK11-00-0008) were used to create the anaemia model due to the renal functional failure by a two-step nephrectomy [27]. ⅚ nephrectomy was performed on rats with general anaesthesia by two separate operations under sterile conditions. After ⅔ of the left kidney was resected, the rats were allowed to recover for twenty days. The right kidney was then resected. Antibiotics were administrated to prevent infection after each operation. In total, ⅚ of the kidney tissue from each rat was resected. The nephrectomized rats gradually developed renal function insufficiency and anaemia. Anaemia stabilized 50 days after the nephrectomy, and the rats were then randomly grouped (9 per group) to begin administration of the EPOs. Each group of rats was treated with one combination of one dose (2.5, 12.5, 62.5 μg/kg), one injection route (i.v. through the tail vein or s.c.) and one injection schedule (once per week or once every 2 weeks). The control group and model group of rats were injected with an equal volume of carrier solution. Treatment lasted for 4 weeks and the total observation time was 6 weeks.

All doses (2.5, 12.5, 62.5 μg/kg) of rHuEPO-FcG , administrated subcutaneously once per week, induced dose-dependent elevation of Hb levels compared to the model control group that did not receive EPO treatment. Both 12.5 and 62.5 μg/kg of rHuEPO or darbepoetin, administrated subcutaneously once per week also induced elevation of Hb levels. The increased levels of Hb in both groups treated with 12.5 or 62.5 μg/kg of rHuEPO-FcG were significantly higher than those in groups treated with 12.5 or 62.5 μg/kg of rHuEPO respectively. The Hb levels in 62.5 μg/kg of rHuEPO-FcG-treated group were also slightly higher than that in 62.5 μg/kg of darbepoetin-treated group. After stopping treatment, the decrease of Hb levels in the 62.5 μg/kg of rHuEPO-FcG-treated group was much slower and the Hb levels remained higher than those of both normal control and model control groups until the end of observation (two weeks after treatment), indicating a stronger and/or a prolonged erythopoietic stimulation (summarized in FIG. 9).

For treatment with subcutaneous injection once every two weeks, only 12.5 or 62.5 μg/kg of the three EPOs were administrated (FIG. 10). 12.5 μg/kg of rHuEPO barely increased Hb levels compared to the model control group, and the weak erythropoietic response in the 62.5 μg/kg of rHuEPO-treated group failed to bring the Hb levels to normal in comparison with the normal control group. Treatments of either rHuEPO-FcG or darbepoetin at the doses of 12.5 or 62.5 μg/kg induced significant elevation of Hb levels that was higher than that of the normal control group, indicating the effective correction of anaemia by both rHuEPO-FcG and darbepoetin. No significant differences were observed between same doses of rHuEPO-FcG and darbepoetin in terms of efficacy. The high dose of 62.5 μg/kg resulted in the persistent increase of erythropoiesis until the termination of the observation (two weeks post treatment). This further suggested that rHuEPO-FcG and darbepoetin exhibit the property of long-lasting stimulation of erythropoiesis in vivo, which in turn could be translated to the reduction of administration frequency to patients clinically.

While darbepoetin has been approved for clinical application with less-frequent injections to increase patient compliance and reduce the work burden on health care providers, these experimental data strongly indicate that rHuEPO-FcG disclosed herein has at least comparable potential benefits. As discussed above, darbepoetin, as a mutant analog of the human EPO molecule containing additional sugar compounds (increased glycosylation), may have an increased risk of inducing immunogenesis in vivo due to alteration of native three dimensional structures. Only long-term observation of patients undergoing treatment with darbepoetin will reveal the immunogenic risks of darbepoetin. In contrast, rHuEPO-FcG, which does not modify the EPO molecule portion, has a carbohydrate content identical or closely similar to that of native human EPO. The amount of sialic acids in the inventors' pure rHuEPO-FcG protein were approximately 10.0 mmol/mmol EPO, consistent with the reported parameters of rHuEPO. The Fc portion of rHuEPO-FcG, with no external amino acid(s)/linking peptide, represents the general structure of human IgG 1, and should not generate an immunogenic response. If approved clinically, rHuEPO-FcG may provide a better choice for patients than currently available rHuEPO and EPO analogs, especially those in need of long-term administration.

Intravenous injection once every two weeks, with each of rHuEPO-FcG and darbepoetin (62.5 μg/kg), induced identical increases of Hb levels in the rats with renal anaemia far above the normal Hb levels in the normal control rats (FIG. 11). This further demonstrates the persistent stimulation of erythropoiesis by rHuEPO-FcG.

Data derived from cell culturing experiments of bone marrow cells collected from the ⅚ nephrectomized rats after treatments (once per week s.c. (FIG. 12A) or per two weeks, s.c. (FIG. 12B) or i.v. (FIG. 12C)) showed that rHuEPO-FcG , rHuEPO and darbepoetin all stimulated the formation of CFU-E and BFU-E. The potencies of rHuEPO-FcG and darbepoetin were similar and stronger than that of rHuEPO.

Blood urinonitrogen (BUN) and creatinine levels were similar in the treated groups and model control group. The levels of serum Fe in all the treated groups were higher than that of the model control group. Pathological examinations revealed increased distribution of red blood cell (RBC)-related cells in bone marrow and spleen of all EPO-treated rats.

8. Pharmacokinetic Studies of rHuEPO-FcG in Rhesus Monkeys

As discussed above, the inventors have designed rHuEPO-FcG in such a way that the EPO portion of the fusion protein retains the functional properties of natural EPO, such as stimulating erythropoiesis, and the Fc fragment of human IgG 1 allows the retention of the fusion protein in circulation, thus extending its half-life in vivo. The above animal studies have demonstrated the erythropoietic activities of rHuEPO-FcG are enhanced in comparison with rHuEPO. The inventors have also conducted pharmacokinetic studies to determine the in vivo half-life of rHuEPO-FcG in comparison to that of rHuEPO. Primates were used to generate data as they are biologically very similar to human beings.

Study design was based on literature reports and the experiments were conducted according to the general guidelines of pharmacokinetics. Two groups of Rhesus monkeys with 5 monkeys in each group (3-5 kg, purchased from the Experiment Animal Center, AMMS, China) were injected intravenously with 5 μg/kg of rHuEPO-FcG or rHuEPO, respectively. Blood samples were taken before and at 0.017, 0.167, 0.5, 1, 2, 4, 8, 12, 24, 48, 96, 168 and 240 h after injection. Sera were collected by centrifugation and the serum rHuEPO-FcG or rHuEPO levels were determined by using human erythropoietin enzyme-linked immunosorbent assay (ELISA) kits (purchased from R&D Systems, Minneapolis, USA). The average half-life of rHuEPO-FcG and rHuEPO injected intravenously was 35.24+/−5.15 h and 8.72+/−1.69 h respectively.

To observe the bioavailability of rHuEPO-FcG, 5 ug/kg of rHuEPO-FcG was injected subcutaneously to 5 Rhesus monkeys. Blood samples were taken before and 1, 2, 5, 8, 10, 12, 15, 24, 48, 72, 96, 168 and 240 h after the injection, and the serum levels of rHuEPO-FcG were determined by the R&D kits. (FIG. 13.) The bioavailability index was calculated as 35.71+/−5.37% with the subcutaneous injection. This is essentially identical to the reported bioavailability figures of darbepoetin-alpha (ARANESP) in patients with chronic renal failure.

This data demonstrates that rHuEPO-FcG has a significantly prolonged half-life in primates, and the in vivo half-life of rHuEPO-FcG is at least four fold longer than that of rHuEPO manufactured by Kirin Beer Brewing Co. of Japan. The prolonged half-life in vivo likely contributes to the enhanced erythropoietic activity of rHuEPO-FcG.

9. Immunogenicity of rHuEPO-FcG in Macaca fascicularis

As indicated above, the design of rHuEPO-FcG fusion protein intentionally avoids or minimizes changes of the immunogenic properties of the rHuEPO-FcG fusion protein. The inventors avoided including/adding any external amino acid(s) or linking peptide sequences in the fusion protein. According to one embodiment of the invention, the HuEPO-Fc fusion protein shown in FIG. 1B only contains the polypeptide sequences of the natural EPO protein and the Fc fragment (hinge region, CH2, CH3) of human IgG 1, and thus should not induce an immunogenic response nor the production of antibodies against rHuEPO-FcG protein.

Primate studies were conducted to observe the immunogenicity of rHuEPO-FcG protein. Ten crab-eating macaques (Macaca fascicularis) (male/female=5/5, ˜5 years old, average weight of male 4.0±0.3 kg, female is 2.9±0.4 kg, purchased from Laboratory Animal Center, AMMS, China) were injected subcutaneously with 5 μg/kg of purified rHuEPO-FcG three times per week for four weeks, and two were injected with an equal volume of carrier solution as the control animals. Sera were collected once a week for 5 weeks (1 week post-treatment) and tested for the specific antibodies against rHuEPO-FcG by ELISA using purified rHuEPO-FcG (5 μg/ml) as the coating antigen. In addition, RBC counts and Hb levels in the peripheral blood were also determined within the experimental period. The resulting data shows that, while enhancement of erythropoiesis in the rHuEPO-FcG -treated macaques was observed (the mean RBC numbers increased from 4.74×109/ml to 6.67×109/ml and the mean Hb levels increased from 12.2 g/dl to 13.7 g/dl), rHuEPO-FcG did not induce the production of any detectable specific antibodies against the fusion protein. These results indicate that rHuEPO-FcG fusion protein does not cause immunogenicity in primates.

10. Acute Toxicity Studies of rHuEPO-FcG in Normal Mice

To assess the safety of rHuEPO-FcG fusion protein, acute toxic studies were conducted in animals.

Two groups of BALB/c mice (n =20, equal numbers of male and female, 5-6 weeks old, the average weight of female is 15.8±0.4 g, male is 15.9±0.6 g, purchased from Chinese Academy of Medicine, China) were injected intravenously once with an excessive amount of purified rHuEPO-FcG (male=13.3 mg/kg, female=13.2 mg/kg) or equal volume of the carrier solution via their tail veins. In addition to observing the instant reaction following injection, general behaviour and status, activities, eating and defecation patterns and changes were monitored and recorded daily for 14 days. All mice were also weighed at day 7 and day 14. At day 15 post-injection, anatomical examination of the main organs of the mice were conducted. Pathologic examination were to be conducted if any unusual changes or suspicious changes of the organs were observed.

All mice in the 2 groups had no obvious instant reaction following injection. Within the period of 14 days, no obvious changes of behaviour, activities, eating and defecation patterns were observed. Moreover, the weight of the mice in both groups increased steadily during the testing period, and no apparent differences were found between the 2 groups on day 7 or day 14 post injection. No abnormal or pathologic changes were detected in the tissues of brain, lung, heart, liver and kidney. These results indicate that administration of an excessive amount of rHuEPO-FcG, far more than required for exhibiting the normal erythropoiesis function, is safe and had no apparent toxic effects.

11. Comparison of Wild Type and Mutated Fusion Proteins of rHuEPO-FcC and rHuEPO-FcG

Investigations were also conducted to compare wild type and mutated versions of proteins of HuEPO-Fc. As described above, in one embodiment the invention includes a single amino acid mutation at amino acid residue 172 (C172G).

In vivo experiments in mice were conducted to compare the erythropoietic activity of the wild type fusion protein rHuEPO-FcG G with the mutated fusion protein rHuEPO-FcG C and with recombinant human EPO (rHuEPO). For comparison purpose, all the doses of the three proteins used in this example, namely rHuEPO-FcG G, rHuEPO-FcG C and rHuEPO, were the amounts of the EPO molecule portion alone on a molar basis. In respect of the rHuEPO-FcG G and rHuEPO-FcG C proteins, the EPO portion contributes 41.4% of the total rHuEPO-FcG molecular weight as calculated by the ratio of the weight of amino acids of EPO to the weight of the total amino acids of the whole rHuEPO-FcG G and rHuEPO-FcG C molecules (i.e.,166 of 399 amino acids).

rHuEPO-FcG G (stock concentration: 300 μg/ml), rHuEPO-FcG C (stock concentration: 90 μg/ml) and rHuEPO with the natural human EPO structure (6000 IU/0.5 ml, manufactured by Kirin Brewery Co., Japan) were diluted in carrier solution (2.5 mg/ml of human serum albumin, 5.8 mg/ml of sodium citrate, 0.06 mg/ml of citric acid and 5.8 mg/ml of sodium chloride , pH 5.5-5.6). The dose of rHuEPO was calculated according to its activity/amount ratio. BALB/c mice (9 to 10 weeks old, weighing 18-22 g, equal numbers of male and female, purchased from Experiment Animal Center, AMMS, China) were grouped randomly with 8 in each group. Each group of mice was treated with one combination of one dose (2.5, 12.5, 62.5 μg/kg), one injection route (s.c.) and one injection schedule (three times per week or once per week). The control group of mice was injected with an equal volume of carrier solution. Treatment lasted for 26 days. Peripheral blood samples (tail vein) for measurement were taken before treatment, on the 2nd, 6th, 9th, 13th, 16th, 19th, 22nd and 26th days of treatment. Hb was measured as the index by absorptiometry. Mean±SD was calculated from the data of each group and a t test was conducted among different groups.

The administration of EPO three times per week to mice induced saturated stimulation of erythropoiesis. As shown in FIG. 14, the mice treated by rHuEPO-FcG G 3 times per week s.c. had significant elevation of Hb levels even at the dose of 2.5 ug/kg at the 9th day after treatment. The elevation of Hb levels in the treated group was dose-dependent. However, saturated elevation of the Hb levels was induced in mice at the dose of 12.5 ug/kg of rHuEPO-FcG G. The elevation of Hb levels induced by 2.5 ug/kg of rHuEPO-FcG G was also greater than that by 2.5 ug/kg of rHuEPO-FcG C and rHuEPO. These results suggested more potent erythropoietic stimulation by rHuEPO-FcG G.

The erythropoietic potency of rHuEPO-FcG G was further explored by reducing the injection times to once per week subcutaneously. As shown in FIG. 15, the rHuEPO-FcG G-treated groups showed dose-dependent elevation of Hb levels at the doses of 12.5, or 62.5 ug/kg. Both doses of 12.5 and 62.5 ug/kg of rHuEPO also induced the elevation of Hb levels to the similar extent, which was much lower than that by 62.5 ug/kg of rHuEPO-FcG G. The rHuEPO-FcG C-treated groups showed significantly lower Hb levels. This strongly indicates that rHuEPO-FcG G has enhanced erythropoietic activity in vivo. It is presumably due to either improved EPO receptor binding/activation by the dimer EPO molecules in rHuEPO-FcG G protein or by the possible prolonged half-life of rHuEPO-FcG G in vivo, or due to the combined effects of both.

The results demonstrated that rHuEPO-FcG G exhibited an enhanced in vivo erythropoietic activity compared to rHuEPO-FcG C and rHuEPO. This enhanced activity appears to be attributable to the single amino acid mutation in the hinge region of the recombinant molecule at residue 172 (FIGS. 2 and 14). The results show that rHuEPO-FcG C exhibited very little erythropoietic activity in normal mice and much less erythropoietic activity compared to rHuEPO-FcG G and rHuEPO.

12. Enhanced Therapeutic Effects of rHuGMCSF-FcG for Neutropenia in 60Co-Irradiated Dogs

The enhanced biological activity of rHuGMCSF-FcG was observed in model dogs with neutropenia induced by 60Co γ-ray irradiation. The efficacy of rHuGMCSF-FcG was also compared with that of native GM-CSF.

rHuGMCSF-FcG (stock concentration: 1.8 mg/ml, purity 98%) and native human rHuGM-CSF (150 μg/vial, manufactured by NCPC GeneTech Biotechnology Development Co., Ltd., China) were diluted in carrier solution (1% of HSA, 1.1% of benzyl alcohol, 40 mg/ml of mannitol, 10 mg/ml of sucrose, and 1.2 mg/ml of tromethamine).

Beagle dogs (male and female in equal number, weighing 8-10 kg, 12-15 months old, purchased from Beijing Xieerxin Institute of BioResources. Licence No. SOCK 2005-0005, China) were divided into 4 groups (4 in each group) randomly: model control, low dose of rHuGMCSF-FcG (10 μg/kg), high dose of rHuGMCSF-FcG (20 μg/kg), and high dose of rHuGMCSF(20 μg/kg). Each dog, with the pelvis shielded by lead blocks, was irradiated by 6.5 Gy of 60Co γ-ray at a rate of 295.54 rad/min. The treatment started from the next day of irradiation by subcutaneous injection, once every other day for rHuGMCSF-FcG, or once every day for rHuGMCSF. The dogs from control group were injected with an equal volume of carrier solution. Injections were given over 10 days and the total observation time was 28 days. After irradiation, the dogs were examined each day for their general clinical conditions. Every other day, peripheral blood was collected for examinations of WBC count, platelet count, RBC count, HB, and hematocrit (Hct).

As shown in FIG. 16, all the irradiated dogs developed neutropenia immediately after irradiation. Since dogs from control group were only injected with carrier solution, their clinical courses reflected natural recovery with no treatment. WBC counts decreased dramatically the day following irradiation and reached a nadir by day 4. The low WBC count lasted for another 4-5 days. After that, it began increasing slowly, indicating the recovery from neutropenia.

Dogs from the three administrated groups also developed similar neutropenia after irradiation, but their WBC counts showed rapid and sustained increases during the course of treatment. All the nadirs of WBC counts were raised compared with control group. Furthermore, the duration of low WBC counts was also shorter. The increasing of WBC reached its peak on the day following the last injection. These results indicate that both rHuGMCSF-FcG and rHuGMCSF induced hematopoietic recovery.

Different levels of activity were observed within the three administrated groups. rHuGMCSF-FcG demonstrated enhanced hematopoietic recovery compared with rHuGMCSF. Despite only being administrated every other day, the dogs injected with rHuGMCSF-FcG showed stronger recovery potency than dogs with rHuGMCSF administrated daily. While the dogs injected with low doses of rHuGMCSF-FcG (10 μg/kg) and high doses of rHuGMCSF (20 μg/kg) showed similar WBC counts and recovery tendency, the WBC counts from dogs with high doses of rHuGMCSF-FcG (20 μg/kg) were twice as high as the other two groups during the entire course of recovery. This dose-dependent, persistent elevation further indicates that rHuGMCSF-FcG possesses enhanced biological activity compared to its native counterpart (FIG. 16).

The enhanced biological activity of rHuGMCSF-FcG in vivo, similar to that discussed in rHuEPO-FcG experiments, is also presumably due to improved GM-CSF receptor binding/activation by the dimer GM-CSF molecules in rHuGMCSF-FcG protein, the possible prolonged half-life of rHuGMCSF-FcG in vivo, or due to the combined effects of both.

As will be apparent to those skilled in the art in the light of the foregoing disclosure, many alterations and modifications are possible in the practice of this invention without departing from the spirit or scope thereof.

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Claims

1. A fusion protein comprising:

a non-immunoglobulin polypeptide comprising a cysteine residue proximal to the C terminal thereof; and
an immunoglobulin component comprising a mutated hinge region, the mutation comprising a point mutated site corresponding in position to the position in a native hinge region of the cysteine residue located nearest the cysteine residue of the non-Ig component, whereby the distance from the cysteine residue of the non-immunoglobulin polypeptide and any remaining cysteine residues of the mutated hinge region is sufficient to prevent the formation of a disulphide bond therebetween.

2. A fusion protein according to claim 1, wherein the non-immunoglobulin polypeptide is selected from the group consisting of a cytokine, a ligand-binding protein, a hormone, a neurotrophin, a neutrophin receptor, a body-weight regulator, a serum protein, a clotting factor, a protease, an extracellular matrix component, an angiogenic factor, an anti-angiogenic factor, an immunoglobulin receptor, a blood factor, a cancer antigen, a statin, a growth factor, a therapeutic peptide, a non-human protein, a non-mammalian protein and a protein toxin.

3. A fusion protein according to claim 2, wherein the cytokine is selected from the group consisting of hematopoietic factor, interferon, interleukin and tumor necrosis factor.

4. A fusion protein according to claim 3, wherein the hematopoietic factor is selected from the group consisting of erythropoietin, granulocyte-macrophage colony stimulating factor and granulocyte colony stimulating factor.

5. A fusion protein according to claim 2, wherein the ligand-binding protein is selected from the group consisting of a CD molecule, CTLA-4, TNF receptor, and interleukin receptor.

6. A fusion protein according to claim 1, wherein the human immunoglobulin component comprises an Fc fragment.

7. A fusion protein according to claim 6, wherein the Fc fragment is derived from an IgG.

8. A fusion protein according to claim 7, wherein the IgG is selected from the group consisting of IgG 1, IgG 2, IgG 3 and IgG 4.

9. A fusion protein according to claim 8, wherein the Fc fragment is a IgG Fc fragment comprising the mutated hinge region and CH2 and CH3 domains.

10. A fusion protein according to claim 9, wherein the IgG Fc fragment derived from IgG 1.

11. A fusion protein according to claim 1 wherein the C-terminal of the non-immunoglobulin polypeptide is directly linked to the N-terminal of the mutated hinge region.

12. A fusion protein according to claim 1, wherein the mutated hinge region comprises at least 9 amino acids.

13. A fusion protein according to claim 12, wherein the mutated hinge region comprises between 10 and 20 amino acids.

14. A fusion protein according to claim 1, wherein the point mutated site comprises a non-cysteine amino acid.

15. A fusion protein according to claim 1, wherein the point mutated site is the sixth amino acid position measured from the N-terminal of the mutated hinge region and comprises a non-cysteine amino acid.

16. A fusion protein according to claim 14, wherein the non-cysteine amino acid is a neutral amino acid.

17. A fusion protein according to claim 14, wherein the non-cysteine amino acid is glycine.

18. A fusion protein according to claim 14, wherein the non-cysteine amino acid is alanine.

19. A fusion protein according to claim 1, wherein the non-immunoglobulin polypeptide is a human granulocyte-macrophage colony stimulating factor or a variant thereof

20. A multimeric protein comprising a plurality of fusion proteins according to claim 1.

21. A multimeric protein according to claim 20 wherein the multimeric protein is a dimer.

22. A method of producing a fusion protein as defined in claim 1 comprising culturing a cell line transfected with a DNA molecule that encodes the sequence of the fusion protein and purifying the protein encoded thereby.

23. A cell line as defined in claim 22, wherein the cell line is a CHO cell line.

24. A method of stimulating white blood cell production in a mammal comprising administering to the mammal a fusion protein according to claim 19.

25. A method according to claim 24 wherein the mammal is a human.

26. A pharmaceutical composition comprising a fusion protein according to claim 19 and a pharmaceutically acceptable carrier, adjuvant or diluent.

27. A method of stimulating white blood cell production in a mammal comprising administering to the mammal a pharmaceutical composition according to claim 26.

28. A method according to claim 27 wherein the mammal is a human.

29. A fusion protein comprising:

a non-immunoglobulin polypeptide; and
an immunoglobulin component comprising a mutated hinge region, the mutation comprising a point mutated site in a hinge region of said component promixate to said polypeptide, whereby a cysteine residue of said hinge region is substituted by a non-cysteine residue.

30. A fusion protein comprising a non-immunoglobulin polypeptide and a human immunoglobulin component, wherein the fusion protein has a prolonged half-life in vivo in comparison to naturally occurring or recombinant native non-immunoglobulin polypeptide.

31. A fusion protein according to claim 30 wherein the non-immunoglobulin polypeptide is directly linked to the human immunoglobulin component.

32. A fusion protein according to claim 30 wherein the non-immunoglobulin polypeptide is linked to the human immunoglobulin component by a synthetic linker.

33. A fusion protein according to claim 30, wherein the half-life of the fusion protein is at least three fold higher than the native non-immunoglobulin polypeptide.

34. A fusion protein according to claim 30, wherein the half-life of the fusion protein is at least four fold higher than the native non-immunoglobulin polypeptide.

35. A fusion protein according to claim 30, wherein the fusion protein has enhanced biological activity in comparison to the native non-immunoglobulin polypeptide.

36. A fusion protein according to claim 30, wherein the non-immunoglobulin polypeptide is selected from the group consisting of a cytokine, a ligand-binding protein, a hormone, a neurotrophin, a neutrophin receptor, a body-weight regulator, a serum protein, a clotting factor, a protease, an extracellular matrix component, an angiogenic factor, an anti-angiogenic factor, an immunoglobulin receptor, a blood factor, a cancer antigen, a statin, a growth factor, a therapeutic peptide, a non-human protein, a non-mammalian protein and a protein toxin.

37. A fusion protein according to claim 36, wherein the cytokine is selected from the group consisting of hematopoietic factor, interferon, interleukin and tumor necrosis factor.

38. A fusion protein according to claim 37, wherein the hematopoietic factor is selected from the group consisting of erythropoietin, granulocyte-macrophage colony stimulating factor and granulocyte colony stimulating factor.

39. A fusion protein according to claim 37, wherein the ligand-binding protein is selected from the group consisting of a CD molecule, CTLA-4, TNF receptor, and interleukin receptor.

40. A fusion protein according to claim 30, wherein the human immunoglobulin component comprises an Fc fragment.

41. A fusion protein according to claim 40, wherein the Fc fragment is derived from an IgG.

42. A fusion protein according to claim 41, wherein the IgG is selected from the group consisting of IgG 1, IgG 2, IgG 3 and IgG 4.

43. A fusion protein according to claim 40, wherein the Fc fragment comprises a hinge region and CH2 and CH3 domains.

44. A fusion protein according to claim 43, wherein the hinge region comprises at least 9 amino acids.

45. A fusion protein according to claim 44, wherein the hinge region comprises between 10 and 20 amino acids.

46. A fusion protein according to claim 45, wherein the hinge region is mutated.

47. A fusion protein according to claim 46, wherein the hinge region is point-mutated.

48. A fusion protein according to claim 47, wherein the point-mutated site corresponds to the position of the first cysteine from the N-terminal of a native hinge region.

49. A fusion protein according to claim 48, wherein the first cysteine is substituted by a non-cysteine amino acid.

50. A fusion protein according to claim 49, wherein the non-cysteine amino acid is a neutral amino acid.

51. A fusion protein according to claim 50, wherein the non-cysteine amino acid is glycine.

52. A fusion protein according to claim 50, wherein the non-cysteine amino acid is alanine.

53. A fusion protein according to claim 30, wherein the non-immunoglobulin polypeptide is a human granulocyte-macrophage colony stimulating factor or a variant thereof

54. A multimeric protein comprising a plurality of fusion proteins according to claim 30.

55. A multimeric protein according to claim 54 wherein the multimeric protein is a dimer.

56. A method of producing a fusion protein as defined in claim 30 comprising culturing a cell line transfected with a DNA molecule that encodes the sequence of the fusion protein and purifying the protein encoded thereby.

57. A cell line as defined in claim 56, wherein the cell line is a CHO cell line.

58. A method of stimulating white blood cell production in a mammal comprising administering to the mammal a fusion protein according to claim 53.

59. A method according to claim 58 wherein the mammal is a human.

60. A pharmaceutical composition comprising a fusion protein according to claim 53 and a pharmaceutically acceptable carrier, adjuvant or diluent.

61. A method of stimulating white blood cell production in a mammal comprising administering to the mammal a pharmaceutical composition according to claim 60.

62. A method according to claim 61 wherein the mammal is a human.

63. A fusion protein comprising the amino acid sequence of SEQ ID NO:2 or a sequence substantially homologous thereto.

64. A recombinant DNA molecule comprising the nucleic acid sequence of SEQ ID NO:1 or a sequence substantially homologous thereto.

65. A fusion protein comprising the amino acid sequence of SEQ ID NO:6 or a sequence substantially homologous thereto.

66. A recombinant DNA molecule comprising the nucleic acid sequence of SEQ ID NO:5 or a sequence substantially homologous thereto.

Patent History
Publication number: 20220127623
Type: Application
Filed: Jun 4, 2021
Publication Date: Apr 28, 2022
Inventors: Haitao WANG (Vancouver), Yong DU (Vancouver), Rui ZHANG (Vancouver), Jing XU (Vancouver), Longbin LIU (Beijing)
Application Number: 17/339,865
Classifications
International Classification: C12N 15/62 (20060101); A61K 47/68 (20060101);