Modified factor VIII

Abstract

Specific amino acid loci of human factor VIII interact with inhibitory antibodies of hemophilia patients after being treated with factor VIII. Modified factor VIII is disclosed in which the amino acid sequence is changed by a substitution at one or more of the specific loci. The modified factor VIII is useful for hemophiliacs, either to avoid or prevent the action of inhibitory antibodies.

Description

FIELD OF THE INVENTION

This invention relates generally to a modified mammalian factor VIII having amino acid substitutions which reduce its immunogenicity and/or antigenicity as compared to the proteins from which they were derived or other factor VIII preparations such as human factor VIII.

BACKGROUND OF THE INVENTION

Blood clotting begins when platelets adhere to the cut wall of an injured blood vessel at a lesion site. Subsequently, in a cascade of enzymatically regulated reactions, soluble fibrinogen molecules are converted by the enzyme thrombin to insoluble strands of fibrin that hold the platelets together in a thrombus. At each step in the cascade, a protein precursor is converted to a protease that cleaves the next protein precursor in the series. Co-factors are required at most of the steps.

Factor VIII circulates as an inactive precursor in blood, bound tightly and non-covalently to von Willebrand factor. Factor VIII is proteolytically activated by thrombin or factor Xa, which dissociates it from von Willebrand factor and activates its procoagulant function in the cascade. In its active form, the protein factor VIIIa is a cofactor that increases the catalytic efficiency of factor IXa toward factor X activation by several orders of magnitude.

People with deficiencies in factor VIII or antibodies against factor VIII who are not treated with factor VIII suffer uncontrolled internal bleeding that may cause a range of serious symptoms, from inflammatory reactions in joints to early death. Severe hemophiliacs, who number about 10,000 in the United States, can be treated with infusion of human factor VIII, which will restore the blood's normal clotting ability if administered with sufficient frequency and concentration. The classical definition of factor VIII is that substance present in normal blood plasma that corrects the clotting defect in plasma derived from individuals with hemophilia A.

The development of antibodies (“inhibitors” or “inhibitory antibodies”) that inhibit the activity of factor VIII is a serious complication in the management of patients with hemophilia. Autoantibodies develop in approximately 20% of patients with hemophilia A in response to therapeutic infusions of factor VIII. In previously untreated patients with hemophilia A who develop inhibitors, the inhibitors usually develops within one year of treatment. Additionally, autoantibodies that inactivate factor VIII occasionally develop in individuals with previously normal factor VIII levels. Inhibitory antibodies (inhibitors) to factor VIII (fVIII) either develop as alloantibodies in hemophilia A patients following fVIII infusions or as autoantibodies in nonhemophiliacs (Hoyer, L. W. and D. Scandella, 1994, “Factor VIII inhibitors: structure and function in autoantibody and hemophilia A patients,” Semin.Hematol. 31:1-5). Antibodies to epitopes in the A2, ap-A3, and C2 domains within the A1-A2-B-ap-A3-C1-C2 fVIII molecule are responsible for all anticoagulant activity in most inhibitor plasmas (Prescott, R. et al., 1997, “The inhibitory antibody response is more complex in hemophilia A patients than in most nonhemophiliacs with fVIII autoantibodies,” Blood 89:3663-3671; Barrow, R. T. et al., 2000, “Reduction of the antigenicity of factor VIII toward complex inhibitory plasmas using multiply-substituted hybrid human/porcine factor VIII molecules,” Blood 95:557-561). The 18-kDa C2 domain, defined as residues Ser2173-Tyr2332 in single chain human fVIII, contains a phospholipid membrane-binding site that is necessary for the normal procoagulant function of fVIII. Human C2-specific anti-fVIII antibodies inhibit this interaction (Arai, M. et al., 1989, “Molecular basis offactor-VIII inhibition by human antibodies—antibodies that bind to the factor-VIII light chain prevent the interaction of factor-VIII with phospholipid,” J. Clin. Invest. 83:1978-1984). Consistent with this, phospholipid protects fVIII from inactivation by fVIII inhibitors (Arai et al., supra; Barrowcliffe, T. W. et al., 1983, “Binding to phospholipid protects factor VIII from inactivation by human antibodies,” J. Lab. Clin. Med. 101:34-43). The C2 domain also contains part of the von Willebrand factor (vWf) binding site (Saenko, E. L. et al., 1994, “A role for the C2 domain of factor binding to von Willebrand factor. J. Biol. Chem. 269:11601-11605; Saenko, E. L. and Scandella, D., 1997, “The acidic region of the factor VIII light chain and the C2 domain together form the high affinity binding site for von Willebrand factor,” J. Biol. Chem. 272:18007-18014). Some inhibitors may act by interfering with this interaction (Shima, M. et al., 1995, “Common inhibitory effects of human anti-C2 domain inhibitor alloantibodies on factor VIII binding to von Willebrand factor,” Br. J. Haematol. 91:714-721; Saenko, E. L. et al., 1996, “Slowed release of thrombin-cleaved factor VIII from von Willebrand factor by a monoclonal and human antibody is a novel mechanism for factor VIII inhibition,” J. Biol. Chem. 271:27424-27431; Gilles, J G. et al., 1999, “Some factor VIII (FVIII) inhibitors recognize a FVIII epitope(s) that is present only on FVIII-vWf complexes,” Thromb. Haemost. 82:40-45).

Patients can be managed by increasing the dose of factor VIII provided the inhibitor titer is low enough. However, often the inhibitor titer is so high that it cannot be overwhelmed by factor VIII. An alternative strategy is to bypass the need for factor VIII during normal hemostasis using factor IX complex preparations (for example, KONYNE®, Proplex®) or recombinant human factor VIIIa. Additionally, since porcine factor VIII usually has substantially less reactivity with inhibitors than human factor VIII, a partially purified porcine factor VIII preparation (HYATE:C®) is used. Many patients who have developed inhibitory antibodies to human factor VIII have been successfully treated with porcine factor VIII and have tolerated such treatment for long periods of time. However, administration of porcine factor VIII is not a complete solution because inhibitors may develop to porcine factor VIII after one or more infusions.

Several preparations of human plasma-derived factor VIII of varying degrees of purity are available commercially for the treatment of hemophilia A. These include a partially-purified factor VIII derived from the pooled blood of many donors that is heat- and detergent-treated for viruses but contain a significant level of antigenic proteins; a monoclonal antibody-purified factor VIII that has lower levels of antigenic impurities and viral contamination; and recombinant human factor VIII, clinical trials for which are underway. Unfortunately, human factor VIII is unstable at physiologic concentrations and pH, is present in blood at an extremely low concentration (0.2 μg/ml plasma), and has low specific clotting activity.

Hemophiliacs require daily replacement offactor VIII to prevent bleeding and the resulting deforming hemophilic arthropathy. However, supplies have been inadequate and problems in therapeutic use occur due to difficulty in isolation and purification, immunogenicity, and the necessity of removing the AIDS and hepatitis infectivity risk. The use of recombinant human factor VIII or partially-purified porcine factor VIII will not resolve all the problems.

The problems associated with the commonly used, commercially available, plasma-derived factor VIII have stimulated significant interest in the development of a better factor VIII product. There is a need for a more potent factor VIII molecule so that more units of clotting activity can be delivered per molecule; a factor VIII molecule that is stable at a selected pH and physiologic concentration; a factor VIII molecule that is less apt to cause production of inhibitory antibodies; and a factor VIII molecule that evades immune detection in patients who have already acquired antibodies to human factor VIII.

U.S. Pat. No. 6,180,371 to Lollar describes amino acid substitutions in the A2 domain of human factor VIII which alter the antigenicity of the resulting factor VIII molecules. The '371 patent does not disclose or suggest specific amino acid substitutions in the C2 domain which reduces antigenicity or immunogenicity as compared to wild-type factor VIII or the corresponding recombinant factor VIII.

U.S. Pat. No. 5,859,204 to Lollar discloses the site specific replacement of amino acids in the 484-509 region of human factor VIII. More specifically, the '204 patent teaches modified factor VIII with amino acid substitutions at positions 485, 487, 488, 489, 492, 495, 501 or 508 relative to the human protein. The '204 patent does not disclose or suggest specific amino acid substitutions in the C2 domain which reduce antigenicity or immunogenicity as compared to wild-type factor VIII or the corresponding recombinant factor VIII.

U.S. Pat. No. 5,888,974 to Lollar et al. discloses hybrid procoagulant factor VIII produced by the isolation and recombination of human and other non-human factor VIII subunits or domains.

U.S. Pat. No. 5,744,446 to Lollar et al. describes hybrid factor VIII having amino acid substitutions in the A2 domain.

U.S. Pat. No. 5,663,060 to Lollar et al. describes hybrid factor VIII comprised of combinations of non-human and human heavy and light chain subunits. U.S. Pat. No. 5,583,209 describes nucleic acids encoding the hybrid factor VIII molecules in the '060 patent.

U.S. Pat. No. 5,364,771 describes purified hybrid factor VIII comprised of human and porcine combinations of the heavy and light subunits. Also disclosed is human factor VIII with porcine A2 domain swapped for the human A2 domain.

U.S. Pat. Nos. 6,180,371; 5,888,974; 5,859,204; 5,744,446; 5,663,060; 5,583,209; and 5,364,771 (all of which are incorporated herein by reference) do not disclose substitutions or suggest specific amino acid substitutions in the C2 domain of factor VIII which reduce antigenicity or immunogenicity as compared to wild-type factor VIII or the corresponding recombinant factor VIII. Despite years of intensive research from laboratories around the world, it appears that the invention regarding the C2 domain of factor VIII described in detail herein has not been described or suggested elsewhere.

Pratt et al. (1999, “Structure of the C2 domain of human factor VIII at 1.5 Å resolution,” Nature 402:439-442) have reported the crystal structure of the C2 domain of human factor VIII at 1.5 Å resolution. Pratt et al. reported that the structure partly explains why mutations in the C2 region of factor VIII lead to bleeding disorders. In fact, 21 residues in the C2 region were reported to be sites of deleterious point mutations in patients with hemophilia A. For example, V2223 is known to be a position where a point mutation occurs and is associated with bleeding disorders. Thus, one of ordinary skill in the art would not expect V2223 to be a reasonable candidate for substitution to provide modified factor VIII for therapeutic activity. Indeed, Shima et al. report C2 binding antibody inhibitors interfere with factor VIII with respect to phospholipid and Von Willebrand factor binding. Thus, it is taught by Pratt et al. that C2 inhibitors, i.e., those related to some bleeding disorders in individuals with hemophilia A, interfere with the binding of the C2 domain to phospholipid and Von Willebrand factor. This conclusion, combined with their determination that M2199, F2200, L2251, L2252, V2223, and R2220 appear at the protein-phospholipid interface, suggests that mutation of these residues would lead to altered phospholipid and/or Von Willebrand binding along with an associated increase in bleeding disorders. It is not clear from these studies which amino acid residues and corresponding substitutions would lead to improved factor VIII molecules.

Unexpectedly it was discovered by the inventor of the instant invention that mutations in the 3 hydrophobic feet identified in the recently available x-ray structure for the C2 domain of factor VIII have reduced binding to inhibitory antibodies, improved properties, and/or reduced immunogenicity.

It is therefore an object of the present invention to provide a factor VIII that corrects hemophilia in a patient deficient in factor VIII or having inhibitors to factor VIII.

It is a further object of the present invention to provide methods for treatment of hemophiliacs.

It is still another object of the present invention to provide a factor VIII that is stable at a selected pH and physiologic concentration.

It is yet another object of the present invention to provide a factor VIII that has greater coagulant activity than human factor VIII.

SUMMARY OF THE INVENTION

The present invention generally relates to compositions comprising recombinant mammalian factor VIII. The composition of the invention comprise isolated, purified recombinant mammalian factor VIII molecules with coagulant activity wherein the recombinant factor VIII has amino acid substitutions in the C2 domain which reduce antigenicity as compared to the proteins from which they were derived or other factor VIII preparations. DNA sequences encoding the novel compositions of the invention as well as methods of producing the novel compositions comprising factor VIII are also provided. Methods of treating patients in need of treatment with factor VIII are also within the scope of this invention.

A first embodiment of the invention provides novel compositions comprising recombinant mammalian factor VIII with amino acid substitution(s) in the C2 domain. The amino acid substitution(s) in the C2 domain of the modified recombinant factor VIII reduce the anticoagulant activity of inhibitory antibodies as compared to the proteins from which they were derived or other available factor VIII preparations. The novel composition of this embodiment have coagulant activity and reduced binding to inhibitory antibodies. Substitutions at residues that participate in binding of fVIII to phospholipid membranes and/or to inhibitory antibodies are preferred. Preferred substitutions at positions homologous to human factor VIII include, but are not limited to, Met2199, Phe2200, Val2223, Leu2251, and Leu2252. The novel compositions of this embodiment can be a single mutant, a double mutant, a triple mutant, or a quadruple mutant. Examples of amino acid substitutions of the invention include, but are not limited to, Met2199Ile, Phe2200Leu, Leu2252Phe, Met2199Ile/Phe2200Leu,Val2223Ala/Lys2227Glu, Met2199Ile/Phe2200Leu/Va2223 Ala/Lys2227Glu, all of which are referenced to the human factor VIII numbering system wherein amino acid number 1 is the amino terminal alanine of mature factor VIII. Substitutions in either recombinant porcine or human factor VIII are preferred.

A second embodiment of the invention provides novel hybrid factor VIII compositions comprising recombinant factor VIII with amino acid substitution(s) in the C2 domain. The novel compositions of this embodiment are constructed by preparing hybrid factor VIII with amino acid substitutions in the C2 domain. The other domains of factor VIII may be derived from a variety of mammals such as human, mouse, pig, rat, and canine and so on. The novel compositions of this embodiment have coagulant activity and reduced binding to inhibitory antibodies. Examples of amino acid positions that can be mutated to provided the novel compositions of this embodiment include, but are not limited to, Met2199, Phe2200, Val2223, Leu2251, and Leu2252, all of which are referenced to human factor VIII. Examples of amino acid substitutions in the C2 domain encompassed within this embodiment include, but are not limited to, Met2199Ile, Phe2220Leu, Leu2252Phe, Met2199Ile/Phe2200Leu,Val2223Ala/Lys2227Glu, Met2199Ile/Phe2200Leu/-Val2223Ala/Lys2227Glu, all of which are referenced to the human factor VIII.

Another embodiment of the invention provides DNA sequences comprising coding sequences for the novel compositions of the invention. Yet another embodiment of the invention provides methods of producing the novel compositions of the invention.

The invention also provides a method for reducing the immunogenicity of factor VIII molecules as well as recombinant factor VIII with reduced immunogenicity produced by the method. In particular, modified recombinant factor VIII molecule and methods of making such molecules with reduced immunogenicity that have substitutions in the C2 domain are described.

Also provided are pharmaceutical compositions and methods for treating patients having factor VIII deficiency comprising administering recombinant factor VIII and hybrid version thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 . Putative fVIII residues involved in phospholipid binding. Shown are aligned sequences of the C2 domains of human, HF8 (amino acid residues 2173 to 2332 in SEQ ID NO: 2),(Vehar, G. A. et al., supra, 1984; Toole, J. J. Ct al., 1984, “Molecular cloning of a cDNA encoding human antihaemophilic factor” Nature 312:342-347), porcine, PF8 (SEQ ID NO:19), (Healey, J. F. et al., 1996, “The cDNA and derived amino acid sequence of porcine factor VIII,” Blood 88:4209-4214), murine, MF8 (SEQ ID NO: 20), (Elder, B. et al., 1993, “Sequence of the murine factor VIII cDNA,” Genomics 16:374-379) and canine, CF8 (SEQ ID NO: 21), (Cameron, C. et al., 1998, “The canine factor VIII cDNA and 5′ flanking sequence,” Thromb.Haemostas. 79:317-322) fVIII. Proposed phospholipid-binding residues in human fVIII (Pratt, K. P. et al., 1999, “Structure of the C2 domain of human factor VIII at 1.5 Åresolution,” Nature 402:439-442) and homologous residues are underlined and shown in bold.

FIG. 2 . Mutated sites in the human fVIII C2 domain. A. Ribbon diagram showing hydrophobic residues proposed to be involved in phospholipid membrane binding and Lys2227, one of the four putative positively-charged binding residues (Pratt, K. P. et al., 1999, “Structure of the C2 domain of human factor VIII at 1.5 Å resolution,” Nature 402:439-442). Met2199, Phe2200, Val2223, Lys2227, and Leu2252 were mutated in this study. Leu2251, which is conserved in human, porcine, murine, and canine fVIII, was not mutated. B. Space filling model rotated, as if looking up from the membrane.

FIG. 3 . Bethesda titers of patient polyclonal anti-fVIII antibodies. Recombinant fVIII was diluted into hemophilia A plasma and Bethesda titers of antibodies AA, AJ, HR, LK, and RvR were determined as described in “Materials and Methods”. Shown are means and standard deviations determined by nonlinear least-squares regression analysis. C2 D1 is the Met2199Ile/Phe2200Leu double mutant. C2 D2 is the Val2223Ala/Lys2227Glu double mutant. C2 Q is the Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu quadruple mutant. HP20 is a B-domainless hybrid human/porcine fVIII molecule containing human A1, A2, ap-A3, and C1 domains and the porcine C2 domain. Confidence levels for differences between mutants and HB- are indicated as “**” at the 99.9% level and “*” at the 99% level. NS, not significant.

FIG. 4 . Bethesda titers of patient monoclonal antibody BO2C11. Abbreviations and notations are as described in FIG. 3 legend.

FIG. 5 . Bethesda titers of murine monoclonal antibody NMC VIII-5. Abbreviations and notations are as described in FIG. 3 legend

DETAILED DESCRIPTION OF THE INVENTION

The present invention generally relates to compositions comprising recombinant mammalian factor VIII. The composition of the invention comprise isolated, purified recombinant mammalian factor VIII molecules with coagulant activity. It was surprisingly discovered that mutations in the C2 domain of factor VIII, in three hydrophobic feet identified in a recently available x-ray structure, reduced the binding of inhibitory antibodies of the mutants as compared to the proteins from which they were derived and/or other factor VIII preparations. Thus, the novel compositions of the invention comprise recombinant factor VIII with amino acid substitutions in the C2 domain which reduce antigenicity as compared to the proteins from which they were derived. Furthermore, the invention also provides recombinant factor VIII with amino acid substitutions in the C2 domain which reduce antigenicity as compared to other available factor VIII preparations. Related embodiments of the invention provide for methods of treating patients in need offactor VIII treatment, methods of producing the novel recombinant factor VIII compositions of the invention, DNA sequences comprising coding sequences of the novel recombinant factor VIII proteins, and pharmaceutical compositions comprising the novel factor VIII proteins.

The present invention further provides active recombinant hybrid factor VIII molecules or fragments thereof, the nucleic acid sequences encoding these hybrids, methods of preparing and isolating them, and methods for characterizing them. These hybrids comprise human/animal, animal/animal, or other such hybrid factor VIII molecules, and further comprise at least one specific amino acid sequence in the C2 domain including one or more unique amino acids of the factor VIII of one species substituted for the corresponding amino acid sequence (or amino acid) of the factor VIII of the other species; or comprises at least one sequence in the C2 domain including one or more amino acids having no known sequence identity to factor VIII substituted for specific amino acid sequence in human, animal, or hybrid factor VIII. The resulting recombinant hybrid factor VIII has reduced or no immunoreactivity to factor VIII inhibitory antibodies, compared to human or porcine factor VIII.

A “corresponding” nucleic acid or amino acid or sequence of either, as used herein, is one present at a site in a factor VIII molecule or fragment thereof that has the same structure and/or function as a site in the factor VIII molecule of another species, although the nucleic acid or amino acid number may not be identical. A DNA sequence “corresponding to” another factor VIII sequence substantially corresponds to such sequence, and hybridizes to the sequence of the designated SEQ ID NO. under stringent conditions. A DNA sequence “corresponding to” another factor VIII sequence also includes a sequence that results in the expression of a factor VIII or fragment thereof and would hybridize to the designated SEQ ID NO. but for the redundancy of the genetic code.

A “unique” amino acid residue or sequence, as used herein, refers to an amino acid sequence or residue in the factor VIII molecule of one species that is different from the homologous residue or sequence in the factor VIII molecule of another species.

“Specific activity,” as used herein, refers to the activity that will correct the coagulation defect of human factor VIII deficient plasma. Specific activity is measured in units of clotting activity per milligram total factor VIII protein in a standard assay in which the clotting time of human factor VIII deficient plasma is compared to that of normal human plasma. One unit of factor VIII activity is the activity present in one milliliter of normal human plasma. In the assay, the shorter the time for clot formation, the greater the activity of the factor VIII being assayed. Porcine factor VIII has coagulation activity in a human factor VIII assay.

“Expression” refers to the set of processes that occur whereby genetic information is utilized to yield a product. A DNA encoding the amino acid sequence of porcine factor VIII can be “expressed” within a mammalian host cell to yield modified factor VIII protein. The materials, genetic structures, host cells and conditions which permit expression of a given DNA sequence to occur are well-known in the art and can be manipulated to affect the time and amount of expression, as well as the intra- or extra-cellular location of the expressed protein. For example, by including DNA encoding a signal peptide at the 5′ end of the DNA encoding porcine factor VIII (the 5′ end being, by convention, that end encoding the NH 2 terminus of the protein) the expressed protein becomes exported from the interior of the host cell into the culture medium. Providing a signal peptide coding DNA in combination with the porcine factor VIII coding DNA is advantageous because the expressed factor VIII is exported into the culture medium which simplifies the process of purification. A preferred signal peptide is a mammalian factor VIII signal peptide.

The human factor VIII cDNA nucleotide and predicted amino acid sequences are shown in SEQ ID NOs: 1 and 2, respectively. Factor VIII is synthesized as an approximately 300 kDa single chain protein with internal sequence homology that defines the “domain” sequence NH 2 -A1-A2-B-A3-C1-C2-COOH. In a factor VIII molecule, a “domain”, as used herein, is a continuous sequence of amino acids that is defined by internal amino acid sequence identity and sites of proteolytic cleavage by thrombin. Unless otherwise specified, factor VIII domains include the following amino acid residues, when the sequences are aligned with the human amino acid sequence (SEQ ID NO: 2): A1, residues Ala1-Arg372; A2, residues Ser373-Arg740; B, residues Ser741-Arg1648; A3, residues Ser1690-Ile2032; C1, residues Arg2033-Asn2172; C2, residues Ser2173-Tyr2332. The A3-C1-C2 sequence includes residues Ser1690-Tyr2332. The remaining segment, residues Glu1649-Arg1689, is usually referred to as the factor VIII light chain activation peptide. Factor VIII is proteolytically activated by thrombin or factor Xa, which dissociates it from von Willebrand factor, forming factor VIIIa, which has procoagulant function. The biological function of factor VIIIa is to increase the catalytic efficiency of factor IXa toward factor X activation by several orders of magnitude. Thrombin-activated factor VIIIa is a 160 kDa A1/A2/A3-C1-C2 heterotrimer that forms a complex with factor IXa and factor X on the surface of platelets or monocytes. A “partial domain” as used herein is a continuous sequence of amino acids forming part of a domain.

“Subunits” of human or animal factor VIII, as used herein, are the heavy and light chains of the protein. The heavy chain of factor VIII contains three domains, A1, A2, and B. The light chain of factor VIII also contains three domains, A3, C1, and C2.

The terms “epitope,” “antigenic site,” and “antigenic determinant,” as used herein, are used synonymously and are defined as a portion of the human, or animal factor VIII or fragment thereof that is specifically recognized by an antibody. It can consist of any number of amino acid residues, and it can be dependent upon the primary, secondary, or tertiary structure of the protein.

The term “immunogenic site,” as used herein, is defined as a region of the human or animal factor VIII, or fragment thereof, that specifically elicits the production of antibody to the factor VIII, or fragment, in a human or animal, as measured by routine protocols, such as immunoassay, e.g. ELISA, or the Bethesda assay, described herein. It can consist of any number of amino acid residues, and it can be dependent upon the primary, secondary, or tertiary structure of the protein. In some embodiments, the hybrid or hybrid equivalent factor VIII or fragment thereof is nonimmunogenic or less immunogenic in an animal or human than human or porcine factor VIII.

“Factor VIII deficiency,” as used herein, includes deficiency in clotting activity caused by production of defective factor VIII, by inadequate or no production of factor VIII, or by partial or total inhibition of factor VIII by inhibitors. Hemophilia A is a type of factor VIII deficiency resulting from a defect in an X-linked gene and the absence or deficiency of the factor VIII protein it encodes.

As used herein, “diagnostic assays” include assays that in some manner utilize the antigen-antibody interaction to detect and/or quantify the amount of a particular antibody that is present in a test sample to assist in the selection of medical therapies. There are many such assays known to those of skill in the art. As used herein, human, porcine or modified porcine factor VIII DNA or fragment thereof and protein expressed therefrom, in whole or in part, can be substituted for the corresponding reagents in the otherwise known assays, whereby the modified assays may be used to detect and/or quantify antibodies to factor VIII. It is the use of these reagents, the factor VIII DNA or fragment thereof or protein expressed therefrom, that permits modification of known assays for detection of antibodies to human or animal factor VIII. Such assays include, but are not limited to ELISAs, immunodiffusion assays, and immunoblots. Suitable methods for practicing any of these assays are known to those of skill in the art. As used herein, the factor VIII or fragment thereof that includes at least one epitope of the protein can be used as the diagnostic reagent. Examples of other assays in which human, porcine or modified porcine factor VIII or fragment thereof can be used include the Bethesda assay and anticoagulation assays.

The term “DNA encoding a protein, such as porcine factor VIII” means a polydeoxynucleic acid whose nucleotide sequence embodies coding information to a host cell for the amino acid sequence of the protein, e.g. porcine factor VIII, according to the known relationships of the genetic code.

The “expression product” of a DNA encoding a human or animal factor VIII or a modified factor VIII is the product obtained from expression of the referenced DNA in a suitable host cell, including such features of pre- or post-translational modification of protein encoded by the referenced DNA, including but not limited to glycosylation, proteolytic cleavage and the like. It is known in the art that such modifications can occur and can differ somewhat depending upon host cell type and other factors, and can result in molecular isoforms of the product, with retention of procoagulant activity. See, e.g. Lind, P. et al., Eur. J. Biochem. 232:1927 (1995), incorporated herein by reference.

An “expression vector” is a DNA element, often of circular structure, having the ability to replicate autonomously in a desired host cell, or to integrate into a host cell genome and also possessing certain well-known features which permit expression of a coding DNA inserted into the vector sequence at the proper site and in proper orientation. Such features can include, but are not limited to, one or more promoter sequences to direct transcription initiation of the coding DNA and other DNA elements such as enhancers, polyadenylation sites and the like, all as well known in the art. The term “expression vector” is used to denote both a vector having a DNA coding sequence to be expressed inserted within its sequence, and a vector having the requisite expression control elements so arranged with respect to an insertion site that it can serve to express any coding DNA inserted into the site, all as well-known in the art. Thus, for example, a vector lacking a promoter can become an expression vector by the insertion of a promoter combined with a coding DNA.

Discovery of Mutations in Factor VIII Which Reduce Binding of Inhibitory Antibodies

Recently, a 1.5 Å X-ray structure of the human fVIII C2 domain was reported (Pratt, K. P. et al., 1999, “Structure of the C2 domain of human factor VIII at 1.5 A resolution,” Nature 402:439-442). Examination of this structure revealed three solvent-exposed hydrophobic “feet” consisting of Met2199/Phe2200, Val2223, and Leu2251/Leu2252. A ring of positively charged residues, including Arg 2213, Arg 2220, Lys 2227, and Lys 2249, surrounds these residues. This motif suggests that membrane binding consists of the insertion of the hydrophobic feet into the membrane bilayer and is stabilized by electrostatic interaction with negatively charged phospholipid.

Most fVIII inhibitors cross-react poorly with porcine fVIII. This observation led to the mapping of a major determinant of the C2 epitope to residues Glu2181-Val2243 using a series of constructs that contained porcine substitutions in the human fVIII C2 domain (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). In the present invention, residues in porcine, murine, or canine fVIII that are homologous to residues Met2199, Phe2200, Val2223, Lys2227, and/or Leu2252 in human fVIII were used as the basis for creating a series of recombinant fVIII molecules. A significant reduction in antigenicity was observed associated with mutations at Met2199, Phe2200, and Leu2252, indicating that these residues participate in binding of fVIII to phospholipid membranes and often to inhibitory antibodies.

FIG. 1 shows the alignment of the human, porcine, murine and canine fVIII C2 domains. At four of the five proposed hydrophobic phospholipid binding residues there is one species that differs from human fVIII: Met2199→Ile (porcine), Phe2200→Leu (canine), Val2223→Ala (canine), and Leu2252→Phe (murine). There is a species difference in only one of the four proposed basic residues, Lys2227→Glu (porcine). Accordingly, Met2199Ile, Phe2200Leu, Val2223Ala, Leu2252Phe, and Lys2227Glu single mutants in human B-domainless fVIII were made. Additionally, two double mutants, Met2199Ile/Phe2200Leu (designated C2 D1) and is Val2223Ala/Leu2252Phe (C2 D2), and a quadruple mutant, Met2199Ile/Phe2200Leu/Val2223Ala/Leu2252Phe (C2 Q) were made. The locations of the mutated residues in the X-ray structure of fVIII are shown in FIG. 2 . Met2199/Phe2200 and Leu2251/Leu2252 project from two β-hairpin loops. Val2223 projects from an adjacent loop and is near Lys2227.

The mutants were stably expressed in serum-free medium from a baby hamster kidney-derived cell line and then were partially purified. The specific coagulant activities of the hybrids based on an ELISA assay were equal or greater than that of HB- as described in “Materials and Methods”, indicating that they were suitable for antigenicity studies. The interaction of the mutants with C2-specific fVIII inhibitors was measured using the Bethesda assay as described in “Materials and Methods”. The results were compared to human B-domainless fVIII (HB-) and a hybrid human/porcine FVIII molecule, HP20, which is human except for substitution of the entire porcine C2 domain (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709).

Most FVIII inhibitors are polyclonal IgG populations directed against epitopes both within and outside the C2 domain (Prescott, R. et al., supra, 1997; Fulcher, C. A. et al. 1985, “Localization of human factor FVIII inhibitor epitopes to two polypeptide fragments,” Proc. Natl. Acad. Sci. USA 82:7728-7732). However, some inhibitors are C2-specific and are useful for evaluating the effects of substitution of non-human sequence into the C2 domain (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). C2-specific polyclonal inhibitors from five patients, AA, AJ, HR, LK, RvR ( FIG. 3 ) were used in these studies. A reduction in antigenicity due to mutations at Met2199, Phe2200, and/or Leu2252 always was observed, although individual inhibitors varied in the residues they recognized. Surprisingly, frequently there was a significant increase in Bethesda titer, most notably with the Val2223Ala mutant. The double mutant Met2199Ile/Phe2200Leu exhibited low antigenicity toward all five antibodies, consistent with the fact that the antigenicity of Met2199Ile and/or Phe2200Leu always was reduced. Paradoxically, the double mutant Val2223Ala/Lys2227Glu displayed a reduction in antigenicity toward all five polyclonal antibodies even though in three cases (AA, AJ, and HR) the corresponding individual mutants displayed unchanged or increased antigenicity. The antigenicity of the quadruple mutant Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu was equal or lower than the single or double mutants. The antigenicity of HP20 was the lowest of all the mutants. This is consistent with the existence of antigenic residues in addition to Met2199, Phe2200, and Leu2252 that were not mutated in this study.

The Bethesda titers of antibodies BO2C11 (Jacquemin, M. G. et al., 1998, “Mechanism and kinetics of factor VIII inactivation: study with an IgG4 monoclonal antibody derived from a hemophilia A patient with inhibitor,” Blood 92:496-506) and NMC VIII-5 (Shima, M., D. et al., 1993, “A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine,” Thromb. Haemost. 69:240-246) toward HB- and the mutant fVIII molecules are shown in FIGS. 4 and 5 , respectively. BO2C11 is a C2-specific human IgG4κ monoclonal antibody derived from transformed B cells of a hemophilia A inhibitor patient. It is the only C2-specific human antibody that has been cloned to date. BO2C11 and NMC VIII-5 both recognize the C2 domain of fVIII and inhibit the binding of fVIII to vWf and phospholipid. NMC VIII-5 can compete for the binding of human polyclonal inhibitors to fVIII. The results with BO2C11 and NMC VIII-5 were similar to those obtained using polyclonal antibody HR (FIG. 3 ). In all three antibodies, Phe2200 is antigenic, whereas Val2223 and Lys2227 appear to reduce antigenicity.

Mutations at Met2199, Phe2200, and/or Leu2252 were associated with a decrease in antigenicity in most of the seven antibodies tested (Table 1), which was frequently pronounced (FIGS. 3 - 5 ). This is consistent with the hypothesis that the Met2199/Phe2200 and Leu2251/Leu2252 loops participate in membrane binding. Even though all seven inhibitors recognized the M2199/Phe2200 loop, the effects of mutations at Met2199 and Phe2200 often differed. For example, Met2199Ile displayed decreased antigenicity and Phe2200Leu displayed increased antigenicity toward antibody AJ, whereas the opposite was true for BO2C11. Thus, the amino acid specificity of AJ and BO2C11 varies, although both recognize the Met2199/Phe2200 loop.

Previously, a series of recombinant hybrid human/porcine FVIII molecules was used to map a major determinant of the C2 epitope(s) to a segment bounded by residues Glu2181-Val2243 (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). The Met2199/Phe2200 loop is contained within this region. The Leu2251/Leu2252 loop was neither included nor excluded by this analysis because porcine FVIII also contains leucines at residues 2251 and 2252. Substitution of the entire porcine C2 domain into human fVIII, which produces a molecule designated HP20, is associated with lower antigenicity than the more limited substitutions made in the present study (FIGS. 3 - 5 ). This indicates that there are residues outside the Met2199/Phe2200 and Leu2251/Leu2252 loops that contribute to binding by C2 inhibitors.

Recently, X-ray structures of two conformations of the factor V C2 domain in the absence of phospholipid were reported (Macedo-Ribeiro, S. et al., 1999, “Crystal structures of the membrane-binding C2 domain of human coagulation factor V,” Nature 402:434-439). The authors proposed a model for phospholipid membrane binding that involves a loop containing tryptophans at positions 26 and 27 (human factor V C2 domain numbering), which are homologous to Met2199 and Phe2200 in fVIII. A considerable amount of evidence exists to support the involvement of this loop in phospholipid membrane binding. An inhibitory monoclonal antibody, HV-1 that blocks the binding of factor V to PS maps to this loop (Kim, S. W. et al., 2000, “Identification of functionally important amino acid residues within the C2-domain of human factor V using alanine-scanning mutagenesis” Biochemistry 39:1951-1958; Ortel, T. L. et al., 1994 “Localization of functionally important epitopes within the second C-type domain of coagulation factor V using recombinant chimeras,” J. Biol. Chem. 269:15898-15905; Ortel, T. L. et al., 1998, “Inhibitory anti-factor V antibodies bind to the factor V C2 domain and are associated with hemorrhagic manifestations,” Blood 91:4188-4196). Substitution of alanine for residues equivalent to Trp26 and Trp27 in factor Va is associated with decreased binding to PS and loss of coagulant activity (Kim, S. W. et al., supra, 2000, “Identification of functionally important amino acid residues within the C2-domain of human factor V using alanine-scanning mutagenesis,” Biochemistry 39:1951-1958).

Additionally, a loop containing Leu79, which is homologous to Leu2251 in fVIII, and a loop containing residues Asn41-Asn51, were also proposed to participate in phospholipid membrane binding based on proximity to the Trp26/Trp27 loop (Macedo-Ribeiro, S. et al., 1999, “Crystal structures of the membrane-binding C2 domain of human coagulation factor V,” Nature 402:434-439). The fVIII segment that is homologous to the Asn41-Asn51loop, His2076-Asn2082, has not been proposed as a phospholipid membrane-binding site (Pratt, K. P., 1999, “Structure of the C2 domain of human factor VIII at 1.5 Å resolution,” Nature 402:439-442). Conversely, the loop in factor V that is homologous to the Val2223 loop in fVIII was not proposed to participate in phospholipid membrane binding. In the present study, Val2223Ala and Lys2227Glu mutations were usually associated with an increase in antigenicity (Table 1). Thus, these results do not support the hypothesis that these residues participate in phospholipid membrane binding. However, it is possible that they do bind phospholipid but are not frequently targeted by inhibitory antibodies.

The two factor V C2 structures have different conformations, designated “open” and “closed”, which are associated with major movements of Trp26 and Trp27 at the phospholipid membrane binding site. These states are proposed to switch the phospholipid membrane binding state to on and off, respectively (Macedo-Ribeiro, S., supra, 1999). The reduction in antigenicity associated with Val2223 and Lys2227 may result because these residues stabilize a similar “closed” conformational state in FVIII that is associated with low affinity membrane and antibody binding. Relaxation of this state by the Val2223Ala and Lys2227Glu mutations would then lead to high affinity antibody binding. Alternatively, Val2223 and Lys2227 may simply interfere with an antigen-antibody lock-and-key interaction that involves high affinity contacts with other fVIII residues (e.g., Met2199, Phe2200, etc.).

The human C2-specific monoclonal antibody, BO2C11, is important to compare to polyclonal inhibitors because of the heterogeneity that may confound the analysis of the latter. The functional properties of BO2C11 are similar to the murine monoclonal antibody NMC VIII-5. Both antibodies inhibit the binding of fVIII to PS and to vWf and promote dissociation of the fVIII-vWf complex (Jacquemin, M. G. et al., 1998, “Mechanism and kinetics of factor VIII inactivation: study with an IgG4 monoclonal antibody derived from a hemophilia A patient with inhibitor,” Blood 92:496-506; Shima, M. et al., 1993, “A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine,” Thromb.Haemost. 69:240-246). These results indicate that Phe2200 but not Met2199 is an important part of the epitope recognized by both antibodies (FIGS. 4 and 5 ). However, NMC VIII-5 recognizes Leu2252 but BO2C11 does not. Val2223 and Lys2227 reduce antigenicity with respect to both antibodies. Thus, BO2C11 and NMC VIII-5 appear to recognize overlapping but not identical epitopes.

The RvR antibody was obtained from a hemophilia A patient who was part of an inhibitor “epidemic” that resulted from exposure to a heat pasteurized FVIII product, CPS-A (Sawamoto, Y. et al., 1998, “C2 domain restricted epitope specificity of inhibitor antibodies elicited by a heat pasteurized product, factor VIII CPS-P, in previously treated hemophilia A patients without inhibitors,” Thromb.Haemostas. 79:62-68). In 1990 and 1991, several previously treated patients without inhibitors promptly developed C2-specific antibodies after exposure to this product in The Netherlands and Belgium. RvR antibodies block the binding of fVIII to both PS and vWf(Sawamoto, Y. et al., supra, 1998). The RvR epitope maps to the N-terminal, Glu2181-Val2243 region of the fVIII C2 domain recognized by most C2 inhibitors (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). The high resolution mapping in the present study indicates that RvR is a typical C2 inhibitor that recognizes primarily the Met2199/Phe2200 and Leu2251/Leu2252 loops. Thus, the immunogenicity associated with the CPS-A appears to be due to enhanced immune recognition of a normal immunodominant epitope rather than to development of a neoepitope.

General Description of Methods

U.S. Pat. No. 5,364,771 described the discovery of hybrid human/porcine factor VIII molecules having coagulant activity, in which elements of the factor VIII molecule of human or pig are substituted for corresponding elements of the factor VIII molecule of the other species. U.S. Pat. No. 5,663,060 describes procoagulant hybrid human/animal and hybrid equivalent factor VIII molecules, in which elements of the factor VIII molecule of one species are substituted for corresponding elements of the factor VIII molecule of the other species.

Since current information indicates that the B domain has no inhibitory epitope and has no known effect on factor VIII function, in some embodiments the B domain is wholly or partially deleted in the active hybrid or hybrid equivalent factor VIII molecules or fragments thereof (“B(−) factor VIII”) prepared by any of the methods described herein.

The human factor VIII gene was isolated and expressed in mammalian cells, as reported by Toole, J. J. et al. (1984) Nature 312:342-347 (Genetics Institute); Gitschier, J. et al.(1984) Nature 312:326-330 (Genentech); Wood, W. I. et al. (1984) Nature 312:330-337 (Genentech); Vehar, G. A. et al. (1984) Nature 312:337-342 (Genentech); WO 87/04187; WO 88/08035; WO 88/03558; U.S. Pat. No. 4,757,006, and the amino acid sequence was deduced from cDNA. U.S. Pat. No. 4,965,199 to Capon et al. discloses a recombinant DNA method for producing factor VIII in mammalian host cells and purification of human factor VIII. Human factor VIII expression on CHO (Chinese hamster ovary) cells and BHKC (baby hamster kidney cells) has been reported. Human factor VIII has been modified to delete part or all of the B domain (U.S. Pat. No. 4,868,112), and replacement of the human factor VIII B domain with the human factor V B domain has been attempted (U.S. Pat. No. 5,004,803). The cDNA sequence encoding human factor VIII and predicted amino acid sequence are shown in SEQ ID NOs: 1 and 2, respectively. In SEQ ID NO: 1, the coding region begins at nucleotide position 208, the triplet GCC being the codon for amino acid number 1 (Ala) of the mature protein as given in SEQ ID NO: 2.

Porcine factor VIII has been isolated from plasma [Fass, D. N. et al. (1982) Blood 59:594]. Partial amino acid sequence of porcine factor VIII corresponding to portions of the N-terminal light chain sequence having homology to ceruloplasmin and coagulation factor V were described by Church et al. (1984) Proc. Natl. Acad. Sci. USA 81:6934. Toole, J. J. et al. (1984) Nature 312:342-347 described the partial sequencing of the N-terminal end of four amino acid fragments of porcine factor VIII but did not characterize the fragments as to their positions in the factor VIII molecule. The amino acid sequence of the B and part of the A2 domains of porcine factor VIII were reported by Toole, J. J. et al. (1986) Proc. Natl. Acad. Sci, USA 83:5939-5942. The CDNA sequence encoding the complete A2 domain of porcine factor VIII and predicted amino acid sequence and hybrid human/porcine factor VIII having substitutions of all domains, all subunits, and specific amino acid sequences were disclosed in U.S. Pat. No. 5,364,771 entitled “Hybrid Human/Porcine factor VIII” issued on Nov. 15, 1994, and in WO 93/20093 published Oct. 14, 1993. The cDNA sequence encoding the A2 domain of porcine factor VIII corresponding to residues 373-740 in mature human factor VIII, as shown in SEQ ID NO: 1, and the predicted amino acid sequence are shown in SEQ ID NOs: 3 and 4, respectively. More recently, the nucleotide and corresponding amino acid sequences of part of the Al domain lacking the first 198 amino acid and of the A2 domain of porcine factor VIII were reported in WO 94/11503, published May 26, 1994. The entire nucleotide sequence encoding porcine factor VIII, including the complete A1 domain, activation peptide, A3, C1 and C2 domains, as well as the encoded amino acid sequence, was finally obtained by Lollar, as disclosed in U.S. Pat. No. 5,859,204, issued Jan. 12, 1999, and in WO 97/49725, published Dec. 31, 1997, both incorporated herein by reference.

Both porcine and human factor VIII are isolated from plasma as a two subunit protein. The subunits, known as the heavy chain and light chain, are held together by a non-covalent bond that requires calcium or other divalent metal ions. The heavy chain of factor VIII contains three domains, A1, A2, and B, which are linked covalently. The light chain of factor VIII also contains three domains, designated A3, C1, and C2. The B domain has no known biological function and can be removed, or partially removed from the molecule proteolytically or by recombinant DNA technology methods without significant alteration in any measurable parameter of factor VIII. Human recombinant factor VIII has a similar structure and function to plasma-derived factor VIII, though it is not glycosylated unless expressed in mammalian cells.

Both human and porcine activated factor VIII (“factor VIIIa”) have three subunits due to cleavage of the heavy chain between the A1 and A2 domains. This structure is designated A1/A2/A3-C1-C2. Human factor VIIIa is not stable under the conditions that stabilize porcine factor Villa, presumably because of the weaker association of the A2 subunit of human factor VIIIa. Dissociation of the A2 subunit of human and porcine factor VIIIa is associated with loss of activity in the factor VIIIa molecule. Yakhyaev, A. et al. (1997) Blood 90:Suppl. 1, Abstract #126, reported binding of A2 domain by low density lipoprotein receptor-related protein, suggesting that cellular uptake of A2 mediated by such binding acts to down-regulate factor VIII activity.

Expression of “B-domainless factor VIII” is enhanced by including portions of the B-domain. The inclusion of those parts of the B domain designated “SQ” [Lind, P. et al. (1995) supra] was reported to result in favorable expression. “SQ” constructs lack all of the human B domain except for 5 amino acids of the B domain N-terminus and 9 amino acids of the B domain C-terminus.

The purified modified factor VIII or fragment thereof can be assayed for immunoreactivity and coagulation activity by standard assays including, for example, the plasma-free factor VIII assay, the one-stage clotting assay, and the enzyme-linked immunosorbent assay using purified recombinant human factor VIII as a standard.

Other vectors, including both plasmid and eukaryotic viral vectors, may be used to express a recombinant gene construct in eukaryotic cells depending on the preference and judgment of the skilled practitioner (see, for example, Sambrook et al., Chapter 16). Other vectors and expression systems, including bacterial, yeast, and insect cell systems, can be used but are not preferred due to differences in, or lack of, glycosylation.

Recombinant factor VIII protein can be expressed in a variety of cells commonly used for culture and recombinant mammalian protein expression. In particular, a number of rodent cell lines have been found to be especially useful hosts for expression of large proteins. Preferred cell lines, available from the American Type Culture Collection, Rockville, Md., include baby hamster kidney cells, and Chinese hamster ovary (CHO) cells which are cultured using routine procedures and media.

The basis for the greater coagulant activity of porcine factor VIII appears to be the more rapid spontaneous dissociation of the human A2 subunit from human factor VIIIa than the porcine A2 subunit from porcine factor VIIIa. Dissociation of the A2 subunit leads to loss of activity, [Lollar, P. et al. (1990) J. Biol. Chem. 265:1688-1692; Lollar, P. et al. (1992) J. Biol. Chem. 267:23652-23657; Fay, P. J. et al. (1992) J. Biol. Chem. 267:13246-13250].

Factor VIII Molecules with Reduced Immunoreactivity

Epitopes that are immunoreactive with antibodies that inhibit the coagulant activity of factor VIII (“inhibitors” or “inhibitory antibodies”) have been characterized based on known structure-function relationships in factor VIII. Presumably, inhibitors could act by disrupting any of the macromolecular interactions associated with the domain structure of factor VIII or its associations with von Willebrand factor, thrombin, factor Xa, factor IXa, or factor X. However, most inhibitory antibodies to human factor VIII act by binding to epitopes located in the 40 kDa A2 domain or 20 kDa C2 domain of factor VIII, disrupting specific functions associated with these domains, as described by Fulcher et al. (1985) Proc. Natl. Acad. Sci. USA 82:7728-7732; and Scandella et al. (1988) Proc. Natl. Acad. Sci. USA 85:6152-6156. In addition to the A2 and C2 epitopes, there may be a third epitope in the A3 or C1 domain of the light chain of factor VIII, according to Scandella et al. (1993) Blood 82:1767-1775. The significance of this putative third epitope is unknown, but it appears to account for a minor fraction of the epitope reactivity in factor VIII.

Anti-A2 antibodies block factor X activation, as shown by Lollar et al. (1994) J. Clin. Invest. 93:2497-2504. Previous mapping studies by deletion mutagenesis described by Ware et al. (1992) Blood Coagul. Fibrinolysis 3:703-716, located the A2 epitope to within a 20 kDa region of the NH 2 -terminal end of the 40 kDa A2 domain. Competition immunoradiometric assays have indicated that A2 inhibitors recognize either a common epitope or narrowly clustered epitopes, as described by Scandella et al. (1992) Throm. Haemostas. 67:665-671, and as demonstrated in U.S. Pat. No. 5,859,204.

Modified factor VIII molecules can be tested in humans for their reduced antigenicity and/or immunogenicity in clinical trials. In one type of trial, designed to determine whether the factor VIII is immunoreactive with inhibitory antibodies, factor VIII is administered, preferably by intravenous infusion, to approximately 25 patients having factor VIII deficiency who have antibodies that inhibit the coagulant activity of therapeutic human factor VIII. The dosage of the animal or modified animal factor VIII is in a range between 5 and 50 Units/kg body weight, preferably 10-50 Units/kg, and most preferably 40 Units/kg body weight. Approximately 1 hour after each administration, the recovery of factor VIII from blood samples is measured in a one-stage coagulation assay. Samples are taken again approximately 5 hours after infusion, and recovery is measured. Total recovery and the rate of disappearance of factor VIII from the samples is predictive of the antibody titer and inhibitory activity. If the antibody titer is high, factor VIII recovery usually cannot be measured. The recovery results are compared to the recovery results in patients treated with plasma-derived human factor VIII, recombinant human factor VIII, plasma-derived porcine factor VIII, and other commonly used therapeutic forms of factor VIII or factor VIII substitutes.

After identification of clinically significant epitopes, recombinant factor VIII molecules can be expressed that have less than or equal cross-reactivity compared with plasma-derived porcine factor VIII when tested in vitro against a broad survey of inhibitor plasmas. Additional mutagenesis in epitopic regions can be done to reduce cross-reactivity. Reduced cross-reactivity, although desirable, is not necessary to produce a product that may have advantages over the existing plasma-derived porcine factor VIII concentrate, which can produce side effects due to contaminant porcine proteins or contaminant infectious agents such as viruses or prions. A recombinant porcine or modified porcine factor VIII molecule will not contain foreign porcine proteins.

Diagnostic Assays

The factor VIII cDNA and/or protein expressed therefrom, in whole or in part, can be used in assays as diagnostic reagents for the detection of inhibitory antibodies to human or animal factor VIII or modified animal VIII in substrates, including, for example, samples of serum and body fluids of human patients with factor VIII deficiency. These antibody assays include assays such as ELISA assays, immunoblots, radioimmunoassays, immunodiffusion assays, and assay of factor VIII biological activity (e.g., by coagulation assay). Techniques for preparing these reagents and methods for use thereof are known to those skilled in the art. For example, an immunoassay for detection of inhibitory antibodies in a patient serum sample can include reacting the test sample with a sufficient amount of the factor VIII to be tested that a detectable complex can be formed with the inhibitory antibodies in the sample of the test factor VIII is indeed antigenic.

Nucleic acid and amino acid probes can be prepared based on the sequence of the modified factor VIII cDNA or protein molecule or fragments thereof. In some embodiments, these can be labeled using dyes or enzymatic, fluorescent, chemiluminescent, or radioactive labels that are commercially available. The amino acid probes can be used, for example, to screen sera or other body fluids where the presence of inhibitors to human, animal, or hybrid human/animal factor VIII is suspected. Levels of inhibitors can be quantitated in patients and compared to healthy controls, and can be used, for example, to determine whether a patient with a factor VIII deficiency can be treated with an animal or modified animal factor VIII. The cDNA probes can be used, for example, for research purposes in screening DNA libraries.

Preparation of Recombinant Factor VIII

Recombinant factor VIII can be produced through the use of eukaryotic protein expression systems. In general, an eukaryotic cell line, which is deficient in a required gene, is transformed with a vector comprising the gene that it has a deficiency for, and the recombinant DNA which one wishes to express. Transformation can be accomplished by techniques such as electroporation or viral delivery. The cell line chosen to produce the protein is selected to be compatible with the protein of interest, capable of continuously expressing the protein of interests, capable of growing on a medium which facilitates purification of the protein of interest, along with other factors known to those skilled in the art. Examples of such techniques are disclosed in European Patent Application 0 302 968 A2 and U.S. Pat. No. 5,149,637 both of which are incorporated by reference in their entirety.

Testing of Recombinant Factor VIII Molecules

The recombinant factor VIII molecules can be tested in humans for their reduced antigenicity and/or immunogenicity in at least two types of clinical trials. In one type of trial, designed to determine whether the recombinant or recombinant hybrid factor VIII is immunoreactive with inhibitory antibodies, recombinant or recombinant hybrid factor VIII is administered, preferably by intravenous infusion, to approximately 25 patients having factor VIII deficiency who have antibodies to factor VIII that inhibit the coagulant activity of therapeutic human or porcine factor VIII. The dosage of the recombinant or recombinant hybrid factor VIII is in a range between 5 and 50 Units/kg body weight, preferably 10-50 Units/kg, and most preferably 40 Units/kg body weight. Approximately 1 hour after each administration, the recovery of factor VIII from blood samples is measured in a one-stage coagulation assay. Samples are taken again approximately 5 hours after infusion, and recovery is measured. Total recovery and the rate of disappearance of factor VIII from the samples is predictive of the antibody titer and inhibitory activity. If the antibody titer is high, factor VIII recovery usually cannot be measured. The recovery results are compared to the recovery of recovery results in patients treated with plasma-derived human factor VIII, recombinant human factor VIII, porcine factor VIII, and other commonly used therapeutic forms of factor VIII or factor VIII substitutes.

In a second type of clinical trial, designed to determine whether the recombinant or recombinant hybrid factor VIII is immunogenic, i.e., whether patients will develop inhibitory antibodies, recombinant or recombinant hybrid factor VIII is administered, as described in the preceding paragraph, to approximately 100 previously untreated hemophiliac patients who have not developed antibodies to factor VIII. Treatments are given approximately every 2 weeks over a period of 6 months to 1 year. At 1 to 3 month intervals during this period, blood samples are drawn and Bethesda assays or other antibody assays are performed to determine the presence of inhibitory antibodies. Recovery assays can also be done, as described above, after each infusion. Results are compared to hemophiliac patients who receive plasma-derived human factor VIII, recombinant human factor VIII, porcine factor VIII, or other commonly used therapeutic forms of factor VIII or factor VIII substitutes.

Pharmaceutical Compositions

Pharmaceutical compositions comprising recombinant or recombinant hybrid factor VIII, alone or in combination with appropriate pharmaceutical stabilization compounds, delivery vehicles, and/or carrier vehicles, are prepared according to known methods, as described in Remington's Pharmaceutical Sciences by E. W. Martin.

In one preferred embodiment, the preferred carriers or delivery vehicles for intravenous infusion are physiological saline or phosphate buffered saline.

In another preferred embodiment, suitable stabilization compounds, delivery vehicles, and carrier vehicles include but are not limited to other human or animal proteins such as albumin.

Phospholipid vesicles or liposomal suspensions are also preferred as pharmaceutically acceptable carriers or delivery vehicles. These can be prepared according to methods known to those skilled in the art and can contain, for example, phosphatidylserine/phosphatidylcholine or other compositions of phospholipids or detergents that together impart a negative charge to the surface, since factor VIII binds to negatively charged phospholipid membranes. Liposomes may be prepared by dissolving appropriate lipid(s) (such as stearoyl phosphatidyl ethanolamine, stearoyl phosphatidyl choline, arachadoyl phosphatidyl choline, and cholesterol) in an inorganic solvent that is then evaporated, leaving behind a thin film of dried lipid on the surface of the container. An aqueous solution of the hybrid factor VIII is then introduced into the container. The container is then swirled by hand to free lipid material from the sides of the container and to disperse lipid aggregates, thereby forming the liposomal suspension.

Recombinant or recombinant hybrid factor VIII can be combined with other suitable stabilization compounds, delivery vehicles, and/or carrier vehicles, including vitamin K dependent clotting factors, tissue factor, and von Willebrand factor (vWf) or a fragment of vWf that contains the factor VIII binding site, and polysaccharides such as sucrose.

Recombinant or recombinant hybrid factor VIII can also be delivered by gene therapy in the same way that human factor VIII can be delivered, using delivery means such as retroviral vectors. This method consists of incorporation of factor VIII cDNA into human cells that are transplanted directly into a factor VIII deficient patient or that are placed in an implantable device, permeable to the factor VIII molecules but impermeable to cells, that is then transplanted. The preferred method will be retroviral-mediated gene transfer. In this method, an exogenous gene (e.g., a factor VIII cDNA) is cloned into the genome of a modified retrovirus. The gene is inserted into the genome of the host cell by viral machinery where it will be expressed by the cell. The retroviral vector is modified so that it will not produce virus, preventing viral infection of the host. The general principles for this type of therapy are known to those skilled in the art and have been reviewed in the literature (e.g., Kohn, D. B. et al. [1989 ] Transfusion 29:812-820).

Recombinant or recombinant hybrid factor VIII can be stored bound to vWf to increase the half-life and shelf-life of the hybrid molecule. Additionally, lyophilization of factor VIII can improve the yields of active molecules in the presence of vWf. Current methods for storage of human and animal factor VIII used by commercial suppliers can be employed for storage of hybrid factor VIII. These methods include: (1) lyophilization of factor VIII in a partially-purified state (as a factor VIII “concentrate” that is infused without further purification); (2) immunoaffinity-purification of factor VIII by the Zimmerman method and lyophilization in the presence of albumin, which stabilizes the factor VIII; (3) lyophilization of recombinant factor VIII in the presence of albumin.

Additionally, hybrid factor VIII has been indefinitely stable at 4° C. in 0.6 M NaCl, 20 mM MES, and 5 mM CaCl 2 at pH 6.0 and also can be stored frozen in these buffers and thawed with minimal loss of activity.

Methods of Treatment

Recombinant or recombinant hybrid factor VIII is used to treat uncontrolled bleeding due to factor VIII deficiency (e.g., intraarticular, intracranial, or gastrointestinal hemorrhage) in hemophiliacs with and without inhibitory antibodies and in patients with acquired factor VIII deficiency due to the development of inhibitory antibodies. The active materials are preferably administered intravenously.

Additionally, recombinant or recombinant hybrid factor VIII can be administered by transplant of cells genetically engineered to produce the hybrid or by implantation of a device containing such cells, as described above.

In a preferred embodiment, pharmaceutical compositions of recombinant or recombinant hybrid factor VIII alone or in combination with stabilizers, delivery vehicles, and/or carriers are infused into patients intravenously according to the same procedure that is used for infusion of human or animal factor VIII.

The treatment dosages of recombinant or recombinant hybrid factor VIII composition that must be administered to a patient in need of such treatment will vary depending on the severity of the factor VIII deficiency. Generally, dosage level is adjusted in frequency, duration, and units in keeping with the severity and duration of each patient's bleeding episode. Accordingly, the hybrid factor VIII is included in the pharmaceutically acceptable carrier, delivery vehicle, or stabilizer in an amount sufficient to deliver to a patient a therapeutically effective amount of the hybrid to stop bleeding, as measured by standard clotting assays.

Factor VIII is classically defined as that substance present in normal blood plasma that corrects the clotting defect in plasma derived from individuals with hemophilia A. The coagulant activity in vitro of purified and partially-purified forms offactor VIII is used to calculate the dose offactor VIII for infusions in human patients and is a reliable indicator of activity recovered from patient plasma and of correction of the in vivo bleeding defect. There are no reported discrepancies between standard assay of novel factor VIII molecules in vitro and their behavior in the dog infusion model or in human patients, according to: Lusher, J. M. et al. 328 New Engl. J. Med. 328:453-459; Pittman, D. D. et al., (1992) Blood 79:389-397; and Brinkhous et al. (1985) Proc. Natl. Acad. Sci. 82:8752-8755.

Usually, the desired plasma factor VIII level to be achieved in the patient through administration of the recombinant or recombinant hybrid factor VIII is in the range of 30-100% of normal. In a preferred mode of administration of the recombinant or recombinant hybrid factor VIII, the composition is given intravenously at a preferred dosage in the range from about 5 to 50 units/kg body weight, more preferably in a range of 10-50 units/kg body weight, and most preferably at a dosage of 20-40 units/kg body weight; the interval frequency is in the range from about 8 to 24 hours (in severely affected hemophiliacs); and the duration of treatment in days is in the range from 1 to 10 days or until the bleeding episode is resolved. See, e.g., Roberts, H. R., and M. R. Jones, “Hemophilia and Related Conditions—Congenital Deficiencies of Prothrombin (Factor II, Factor V, and Factors VII to XII),” Ch. 153, 1453-1474, 1460, in Hematology , Williams, W. J., et al., ed. (1990). Patients with inhibitors may require more recombinant or recombinant hybrid factor VIII, or patients may require less recombinant or recombinant hybrid factor VIII because of its higher specific activity than human factor VIII or decreased antibody reactivity or immunogenicity. As in treatment with human or porcine factor VIII, the amount of recombinant or recombinant hybrid factor VIII infused is defined by the one-stage factor VIII coagulation assay and, in selected instances, in vivo recovery is determined by measuring the factor VIII in the patient's plasma after infusion. It is to be understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.

Treatment can take the form of a single intravenous administration of the composition or periodic or continuous administration over an extended period of time, as required. Alternatively, recombinant or recombinant hybrid factor VIII can be administered subcutaneously or orally with liposomes in one or several doses at varying intervals of time.

Factor VIII can also be used to treat uncontrolled bleeding due to factor VIII deficiency in hemophiliacs who have developed antibodies to human factor VIII. In this case, coagulant activity that is superior to that of human or animal factor VIII alone is not necessary. Coagulant activity that is inferior to that of human factor VIII (i.e., less than 3,000 units/mg) will be useful if that activity is not neutralized by antibodies in the patient's plasma.

The recombinant or recombinant hybrid factor VIII molecule and the methods for isolation, characterization, making, and using it generally described above will be further understood with reference to the following non-limiting examples.

EXAMPLES

Materials—Citrated hemophilia A plasma and normal pooled human plasma (FACT) were purchased from George King Biomedical, Inc. (Overland Park, Kans.). Heparin-Sepharose was purchased from Sigma Chemical Co.(St. Louis, Mo.). Fetal bovine serum, geneticin, penicillin, streptomycin, DMEM/F12 medium and AIM-V medium were purchased from Life Technologies, Inc. (Gaithersburg, Md.). Pfu DNA polymerase and the phagemid pBlueScript II KS − were purchased from Stratagene (La Jolla, Calif.). Murine anti-human fVIII monoclonal antibodies ESH4 and ESH8 were purchased from American Diagnostica (Greenwich, Conn.). The murine fVIII C2-specific inhibitory monoclonal antibody NMC VIII-5 was obtained from Dr. Midori Shima, Nara Medical College, Japan. A human fVIII C2-specific IgG4κ monoclonal antibody, BO2C11, which was cloned from a transformed B cell line from patient with hemophilia, was prepared as described previously (Jacquemin, M. G. et al., 1998, “Mechanism and kinetics of factor VIII inactivation: study with an IgG4 monoclonal antibody derived from a hemophilia A patient with inhibitor,” Blood 92:496-506). Citrated human plasmas from five inhibitor patients, AA, AJ, HR LK, and RvR, were obtained from Dr. Dorothea Scandella. They were used either without further purification (HR, RvR, and AJ) or as IgG preparations (LK and AA). Inhibitor IgG was prepared as described previously (Scandella, D., L. et al., 1992, “A soluble recombinant factor VIII fragment containing the A2 domain binds to some human anti-factor VIII antibodies that are not detected by immunoblotting,” Thromb.Haemostas. 67:665-671). The inhibitors in HR, LK, AA, and RvR antibodies were specific for the C2 domain as judged by antibody neutralization assays (Prescott, R. et al., 1997, “The inhibitory antibody response is more complex in hemophilia A patients than in most nonhemophiliacs with FVIII autoantibodies,” Blood 89:3663-3671). AJ was identified as a C2-specific using a panel of recombinant hybrid human/porcine FVIII molecules (Barrow, R. T. et al., 2000, “Reduction of the antigenicity of factor VIII toward complex inhibitory plasmas using multiply-substituted hybrid human/porcine factor VIII molecules,” Blood 95:557-561). Albumin-free recombinant full-length fVIII was obtained from the Hyland-Immuno Division of Baxter Healthcare (Deerfield, Ill.). Synthetic oligonucleotides were purchased from Life Technologies, Inc. (Gaithersburg, Md.). Restriction enzymes were purchased from New England Biolabs (Beverly, Mass.) or Promega (Madison, Wis.). A cell line derived from baby hamster kidney cells was obtained from Dr. R. T. A. Macgillivray (Funk, W. D. et al., 1990, “Expression of the amino-terminal half-molecule of human serum transferrin in cultured cells and characterization of the recombinant protein,” Biochemistry 29:1654-1660). A B-domainless fVIII expression vector, designated HB-/ReNeo, containing a NotI site two bases 3′ to the stop codon and ampicillin and geneticin resistance genes was prepared as described previously (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). HSQ/ReNeo, a human B-domainless fVIII molecule containing a fourteen amino acid segment, SerPheSerGlnAsnProPro ValLeuLysArgHisGlnArg, in place of the B domain in human fVIII (Lind, P. et al., 1995, “Novel forms of B-domain-deleted recombinant factor VIII molecules. Construction and biochemical characterization,” Eur. J. Biochem. 232:19-27) was constructed by splicing-by-overlap extension (SOE) mutagenesis (Horton, R. M. et al., 1993, “Gene splicing by overlap extension,” Methods Enzymol. 217:270-279) using HB-/ReNeo as template, essentially as described previously for the corresponding porcine molecule (Healey, J. F. et al., 1998, “Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII,” Blood 92:3701-3709). HP20, a B-domainless hybrid human/porcine fVIII molecule containing human A1, A2, ap-A3, and C1 domains and the porcine C2 domain was prepared as described previously (Healey, J. F., supra, 1998).

Plasmid DNA was purified using a Qiagen Plasmid Maxi Kit (Qiagen, Inc., Valencia, Calif.). PCR reactions were done using a Hybrid OmniGene thermocycler using Pfu DNA polymerase. PCR products were gel purified, precipitated with ethanol, and ligated into plasmid DNA using T4 DNA ligase (Rapid DNA Ligation Kit, Boehringer Mannheim, Indianapolis, Ind.). Insert-containing plasmids were used to transform E. coli Epicurean XL1-Blue cells. All novel fVIII DNA sequences generated by PCR were confirmed by dideoxy sequencing using an Applied Biosystems (Foster City, Calif.) 373a automated DNA sequencer and the PRISM dye terminator kit.

Example 1

Construction of fVIII Mutant cDNAs

Mutations were made in HSQ codons by SOE mutagenesis to produce the following proteins: Met2199Ile (human to porcine), ATG to ATC, Phe2200Leu (human to canine), TTT to TTG, Val2223Ala (human to canine), GTG to GCC, Lys2227Glu (human to porcine), AAA to GAG, Leu2252Phe (human to murine), CTT to TTC, Met2199Ile/Phe2200Leu, ATG to ATC and TTT to TTG, Val2223Ala/Lys2227Glu, GTG to GCC and AAA to GAG, Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu, ATG to ATC, TTT to TTT, GTG to GCC, and AAA to GAG.

HSQ/ReNeo was used as the template in the PCR reactions. The first PCR reaction used the human C1 primer, SEQ ID NO: 3, 5′-GTG GAT TCA TCT GGG ATA AAA CAC-3′, designated H3763+, corresponding to nucleotides 3763-3786 in the HSQ sequence, as the sense primer. The following primers were used as antisense primers:

Met2199Ile,
5′-AGG AGA CCA GGT GGC AAA GAT ATT GGT AAA GTA GGA TGA-3′, SEQ ID NO:4
Phe2200Leu,
5′-TGA AGG AGA CCA GGT GGC CAA CAT ATT GGT AAA GTA GGA-3′, SEQ ID NO:5
Val2223Ala,
5′-CCA CTC TTT TGG ATT ATT GGC CTG AGG TCT CCA GGC ATT-3′, SEQ ID NO:6
Lys2227Glu,
5′-GTC CAC TTG CAG CCA CTC CTC TGG ATT ATT CAC CTG AGG-3′, SEQ ID NO:7
Leu2252Phe,
5′-CTT CAC ATA CAT GCT GGT GAA CAG AGA TTT TAC TCC CTG-3′, SEQ ID NO:8
Met2199Ile/Phe2200Leu,
5′-AGG AGA CCA GGT GGC CAA GAT ATT GGT AAA GTA GGA TGA-3′, and SEQ ID NO:9
Val2223Ala/Lys2227Glu,
5′-CAC TTG CAG CCA CTC CTC TGG ATT ATT GGC CTG AGG TCT CCA GGC-3′. SEQ ID NO:10

The second PCR reaction used the ReNeo primer, SEQ ID NO: 11, 5′-AGT TTT TCT ACA ACA GAG GAA GTG-3′, designated RE1110-, which is 3′ to the C2 domain, as antisense primer. The following primers were used as sense primers:

Met2199Ile,
5′-TCA TCC TAC TTT ACC AAT ATC TTT GCC ACC TGG TCT CCT-3′, SEQ ID NO:12
Phe2200Leu,
5′-TCC TAC TTT ACC AAT ATG TTG GCC ACC TGG TCT CCT TGA-3′, SEQ ID NO:13
Val2223Ala,
5′-AAT GCC TGG AGA CCT CAG GCC AAT AAT CCA AAA GAG TGG-3′, SEQ ID NO:14
Lys2227Glu,
5′-CCT CAG GTG AAT AAT CCA GAG GAG TGG CTG CAA GTG GAC-3′, SEQ ID NO:15
Leu2252Phe,
5′-CAG GGA GTA AAA TCT CTG TTC ACC AGC ATG TAT GTG AAG-3′, SEQ ID NO:16
Met2199Ile/Phe2200Leu,
5′-TCA TCC TAC TTT ACC AAT ATC TTG GCC ACC TGG TCT CCT-3′, and SEQ ID NO:17
Val2223Ala/Lys2227Glu,
5′-GCC TGG AGA CCT CAG GCC AAT AAT CCA GAG GAG TGG CTG CAA GTG-3′. SEQ ID NO:18

The SOE reaction used fragments from the PCR reactions as templates and H3763+ and RE1110 as primers. The SOE product and HSQ/ReNeo ligation fragments were generated using Swa I and Not I.

The Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu cDNA was constructed as follows. The Met2199Ile/Phe2200Leu cDNA was moved into pBluescript II KS- and digested with Bsu36 I. The Val2223Ala/Lys2227Glu cDNA also was digested with Bsu36 I and the appropriate fragments were ligated. The resulting Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu cDNA was moved into ReNeo by digestion with Swa I and Not I.

Example 2

Expression of Recombinant fVIII Molecules

Transfected cell lines were maintained in Dulbecco's modified Eagle's medium-F12 containing 10% fetal bovine serum, 50 U/ml penicillin, and 50 μg/ml streptomycin. Fetal bovine serum was heat inactivated for one hour at 56° C. before use. Mutant cDNAs in ReNeo were stably transfected into BHK cells, selected for geneticin resistance, switched to serum-free, AIM-V medium for expression, and partially purified by heparin-Sepharose chromatography as described previously (Healey, J. F. et al, supra, 1998).

Example 3

FVIII and fVIII Inhibitor Assays

The activity of recombinant fVIII proteins was measured by one-stage clotting assay (Bowie, E. J. W. and C. A. Owen, 1984, “The clinical and laboratory diagnosis of hemorrhagic disorders,” In Disorders of Hemostasis, O. D. Ratnoff and C. D. Forbes, editors. Grune & Stratton, Inc., Orlando, Fla. 43-72). One unit of fVIII is defined as the activity in one ml of normal citrated human plasma. FVIII inhibitor titers were measured by a modification of the Bethesda assay (Kasper, C. K. et al., 1975, “A more uniform measurement of factor VIII inhibitors,” Thromb. Diath. Haemorrh. 34:869-872) as follows. Recombinant FVIII was added to hemophilia A plasma to a final concentration of 0.8-1.2 units per ml and incubated with varying concentrations of inhibitor for 2 hours at 37° C. To determine the 50% inhibition point that defines the Bethesda unit, dilutions of inhibitor were made that produced residual activities that spanned at least the 35% to 65% range. In some cases, replicate dilutions were made, in which case the average was used. An average of 10 dilutions was made for the determination of each Bethesda titer. Semi-logarithmic plots of percent residual activity versus the log of the reciprocal of the inhibitor dilution appeared linear in all cases. The data were fitted by nonlinear regression using the Marquardt algorithm (SigmaPlot 5.0, SPSS, Inc.) to the equation

% Residual activity= m (log x −log x 50 )+50

where the fitted parameter x 50 is the reciprocal dilution that produces 50% inhibition, the fitted parameter m is the slope of the semi-log line and the independent variable x is the reciprocal dilution of the inhibitor sample. The standard error of the estimate (average deviation of data points from the regression line) for 62 Bethesda assays was 10.0±4.0 (mean±1 SD), indicative of the relatively low precision that is inherent in the assay.

The Bethesda titer equals x 50 −1 . The estimate of the standard error (SD) of the Bethesda titer was calculated by multiplying the Bethesda titer by the coefficient of variation of x 50 . The Bethesda titers of fVIII mutants and HB- were compared by Student's t test. The mass concentration of fVIII in partially purified preparations was determined by a sandwich ELISA using ESH4 as capture antibody and biotinylated ESH8 as detection antibody as described previously (Lubin, I. M. et al., 1994, “Elimination of a major inhibitor epitope in factor VIII,” J. Biol. Chem. 269:8639-8641). Full-length recombinant FVIII was used as the standard and values were corrected for the difference in mass between full-length and B-domainless forms of fVIII. Samples were assayed in quadruplicate. The average coefficient of variation was 9.0%. The specific activity of FVIII molecules was calculated by dividing the coagulant activity by the concentration as determined by ELISA. The following values were obtained (units per mg): HB-, 7,800; Met2199Ile, 12,800; Phe2200Leu, 10,200; Val2223Ala, 19,600; Lys2227Glu, 36,200; Leu2252Phe, 10,100; Met2199Ile/Phe2200Leu, 10,000; Val2223Ala/Lys2227Glu, 33,200; Met2199Ile/Phe2200Leu/Val2223Ala/Lys2227Glu, 14,200. The apparent specific activity of some of the mutants is higher than HB-. This may be due to a relatively small decreased ability of the mutants to bind either the capture or detection antibody compared to HB-, leading to an underestimate of fVIII mass and an overestimate of the specific activity.

TABLE 1
Antigenicity of FVIII C2 mutants towards C2-Specific
Inhibitory Antibodies Compared to Human FVIII
			Antigenicity a
	Mutant	Less	Equal	More
	Met2199Ile	4/7	0/7	3/7
	Phe2200Leu	4/7	2/7	1/7
	Val2223Ala	0/7	2/7	5/7
	Lys2227Glu	2/7	1/7	4/7
	Leu2252Phe	4/7	3/7	0/7
	Met2199Ile/Phe2200Leu	6/7	1/7	0/7
	Val2223Ala/Lys2227Glu	4/7	1/7	2/7
	Met2199Ile/Phe2200Leu/	7/7	0/7	0/7
	Val2223Ala/Lys2227Glu
	HP20	7/7	0/7	0/7
	a Significant difference at the 99% confidence level

21 1 9009 DNA Homo sapiens CDS (208)..(7203) 1cagtgggtaa gttccttaaa tgctctgcaa agaaattggg acttttcatt aaatcagaaa 60ttttactttt ttcccctcct gggagctaaa gatattttag agaagaatta accttttgct 120tctccagttg aacatttgta gcaataagtc atgcaaatag agctctccac ctgcttcttt 180ctgtgccttt tgcgattctg ctttagt gcc acc aga aga tac tac ctg ggt gca 234 Ala Thr Arg Arg Tyr Tyr Leu Gly Ala 1 5gtg gaa ctg tca tgg gac tat atg caa agt gat ctc ggt gag ctg cct 282Val Glu Leu Ser Trp Asp Tyr Met Gln Ser Asp Leu Gly Glu Leu Pro 10 15 20 25gtg gac gca aga ttt cct cct aga gtg cca aaa tct ttt cca ttc aac 330Val Asp Ala Arg Phe Pro Pro Arg Val Pro Lys Ser Phe Pro Phe Asn 30 35 40acc tca gtc gtg tac aaa aag act ctg ttt gta gaa ttc acg gtt cac 378Thr Ser Val Val Tyr Lys Lys Thr Leu Phe Val Glu Phe Thr Val His 45 50 55ctt ttc aac atc gct aag cca agg cca ccc tgg atg ggt ctg cta ggt 426Leu Phe Asn Ile Ala Lys Pro Arg Pro Pro Trp Met Gly Leu Leu Gly 60 65 70cct acc atc cag gct gag gtt tat gat aca gtg gtc att aca ctt aag 474Pro Thr Ile Gln Ala Glu Val Tyr Asp Thr Val Val Ile Thr Leu Lys 75 80 85aac atg gct tcc cat cct gtc agt ctt cat gct gtt ggt gta tcc tac 522Asn Met Ala Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Tyr 90 95 100 105tgg aaa gct tct gag gga gct gaa tat gat gat cag acc agt caa agg 570Trp Lys Ala Ser Glu Gly Ala Glu Tyr Asp Asp Gln Thr Ser Gln Arg 110 115 120gag aaa gaa gat gat aaa gtc ttc cct ggt gga agc cat aca tat gtc 618Glu Lys Glu Asp Asp Lys Val Phe Pro Gly Gly Ser His Thr Tyr Val 125 130 135tgg cag gtc ctg aaa gag aat ggt cca atg gcc tct gac cca ctg tgc 666Trp Gln Val Leu Lys Glu Asn Gly Pro Met Ala Ser Asp Pro Leu Cys 140 145 150ctt acc tac tca tat ctt tct cat gtg gac ctg gta aaa gac ttg aat 714Leu Thr Tyr Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn 155 160 165tca ggc ctc att gga gcc cta cta gta tgt aga gaa ggg agt ctg gcc 762Ser Gly Leu Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Ala170 175 180 185aag gaa aag aca cag acc ttg cac aaa ttt ata cta ctt ttt gct gta 810Lys Glu Lys Thr Gln Thr Leu His Lys Phe Ile Leu Leu Phe Ala Val 190 195 200ttt gat gaa ggg aaa agt tgg cac tca gaa aca aag aac tcc ttg atg 858Phe Asp Glu Gly Lys Ser Trp His Ser Glu Thr Lys Asn Ser Leu Met 205 210 215cag gat agg gat gct gca tct gct cgg gcc tgg cct aaa atg cac aca 906Gln Asp Arg Asp Ala Ala Ser Ala Arg Ala Trp Pro Lys Met His Thr 220 225 230gtc aat ggt tat gta aac agg tct ctg cca ggt ctg att gga tgc cac 954Val Asn Gly Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His 235 240 245agg aaa tca gtc tat tgg cat gtg att gga atg ggc acc act cct gaa 1002Arg Lys Ser Val Tyr Trp His Val Ile Gly Met Gly Thr Thr Pro Glu250 255 260 265gtg cac tca ata ttc ctc gaa ggt cac aca ttt ctt gtg agg aac cat 1050Val His Ser Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg Asn His 270 275 280cgc cag gcg tcc ttg gaa atc tcg cca ata act ttc ctt act gct caa 1098Arg Gln Ala Ser Leu Glu Ile Ser Pro Ile Thr Phe Leu Thr Ala Gln 285 290 295aca ctc ttg atg gac ctt gga cag ttt cta ctg ttt tgt cat atc tct 1146Thr Leu Leu Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser 300 305 310tcc cac caa cat gat ggc atg gaa gct tat gtc aaa gta gac agc tgt 1194Ser His Gln His Asp Gly Met Glu Ala Tyr Val Lys Val Asp Ser Cys 315 320 325cca gag gaa ccc caa cta cga atg aaa aat aat gaa gaa gcg gaa gac 1242Pro Glu Glu Pro Gln Leu Arg Met Lys Asn Asn Glu Glu Ala Glu Asp330 335 340 345tat gat gat gat ctt act gat tct gaa atg gat gtg gtc agg ttt gat 1290Tyr Asp Asp Asp Leu Thr Asp Ser Glu Met Asp Val Val Arg Phe Asp 350 355 360gat gac aac tct cct tcc ttt atc caa att cgc tca gtt gcc aag aag 1338Asp Asp Asn Ser Pro Ser Phe Ile Gln Ile Arg Ser Val Ala Lys Lys 365 370 375cat cct aaa act tgg gta cat tac att gct gct gaa gag gag gac tgg 1386His Pro Lys Thr Trp Val His Tyr Ile Ala Ala Glu Glu Glu Asp Trp 380 385 390gac tat gct ccc tta gtc ctc gcc ccc gat gac aga agt tat aaa agt 1434Asp Tyr Ala Pro Leu Val Leu Ala Pro Asp Asp Arg Ser Tyr Lys Ser 395 400 405caa tat ttg aac aat ggc cct cag cgg att ggt agg aag tac aaa aaa 1482Gln Tyr Leu Asn Asn Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys410 415 420 425gtc cga ttt atg gca tac aca gat gaa acc ttt aag act cgt gaa gct 1530Val Arg Phe Met Ala Tyr Thr Asp Glu Thr Phe Lys Thr Arg Glu Ala 430 435 440att cag cat gaa tca gga atc ttg gga cct tta ctt tat ggg gaa gtt 1578Ile Gln His Glu Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val 445 450 455gga gac aca ctg ttg att ata ttt aag aat caa gca agc aga cca tat 1626Gly Asp Thr Leu Leu Ile Ile Phe Lys Asn Gln Ala Ser Arg Pro Tyr 460 465 470aac atc tac cct cac gga atc act gat gtc cgt cct ttg tat tca agg 1674Asn Ile Tyr Pro His Gly Ile Thr Asp Val Arg Pro Leu Tyr Ser Arg 475 480 485aga tta cca aaa ggt gta aaa cat ttg aag gat ttt cca att ctg cca 1722Arg Leu Pro Lys Gly Val Lys His Leu Lys Asp Phe Pro Ile Leu Pro490 495 500 505gga gaa ata ttc aaa tat aaa tgg aca gtg act gta gaa gat ggg cca 1770Gly Glu Ile Phe Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro 510 515 520act aaa tca gat cct cgg tgc ctg acc cgc tat tac tct agt ttc gtt 1818Thr Lys Ser Asp Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Phe Val 525 530 535aat atg gag aga gat cta gct tca gga ctc att ggc cct ctc ctc atc 1866Asn Met Glu Arg Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile 540 545 550tgc tac aaa gaa tct gta gat caa aga gga aac cag ata atg tca gac 1914Cys Tyr Lys Glu Ser Val Asp Gln Arg Gly Asn Gln Ile Met Ser Asp 555 560 565aag agg aat gtc atc ctg ttt tct gta ttt gat gag aac cga agc tgg 1962Lys Arg Asn Val Ile Leu Phe Ser Val Phe Asp Glu Asn Arg Ser Trp570 575 580 585tac ctc aca gag aat ata caa cgc ttt ctc ccc aat cca gct gga gtg 2010Tyr Leu Thr Glu Asn Ile Gln Arg Phe Leu Pro Asn Pro Ala Gly Val 590 595 600cag ctt gag gat cca gag ttc caa gcc tcc aac atc atg cac agc atc 2058Gln Leu Glu Asp Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile 605 610 615aat ggc tat gtt ttt gat agt ttg cag ttg tca gtt tgt ttg cat gag 2106Asn Gly Tyr Val Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu 620 625 630gtg gca tac tgg tac att cta agc att gga gca cag act gac ttc ctt 2154Val Ala Tyr Trp Tyr Ile Leu Ser Ile Gly Ala Gln Thr Asp Phe Leu 635 640 645tct gtc ttc ttc tct gga tat acc ttc aaa cac aaa atg gtc tat gaa 2202Ser Val Phe Phe Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu650 655 660 665gac aca ctc acc cta ttc cca ttc tca gga gaa act gtc ttc atg tcg 2250Asp Thr Leu Thr Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser 670 675 680atg gaa aac cca ggt cta tgg att ctg ggg tgc cac aac tca gac ttt 2298Met Glu Asn Pro Gly Leu Trp Ile Leu Gly Cys His Asn Ser Asp Phe 685 690 695cgg aac aga ggc atg acc gcc tta ctg aag gtt tct agt tgt gac aag 2346Arg Asn Arg Gly Met Thr Ala Leu Leu Lys Val Ser Ser Cys Asp Lys 700 705 710aac act ggt gat tat tac gag gac agt tat gaa gat att tca gca tac 2394Asn Thr Gly Asp Tyr Tyr Glu Asp Ser Tyr Glu Asp Ile Ser Ala Tyr 715 720 725ttg ctg agt aaa aac aat gcc att gaa cca aga agc ttc tcc cag aat 2442Leu Leu Ser Lys Asn Asn Ala Ile Glu Pro Arg Ser Phe Ser Gln Asn730 735 740 745tca aga cac cct agc act agg caa aag caa ttt aat gcc acc aca att 2490Ser Arg His Pro Ser Thr Arg Gln Lys Gln Phe Asn Ala Thr Thr Ile 750 755 760cca gaa aat gac ata gag aag act gac cct tgg ttt gca cac aga aca 2538Pro Glu Asn Asp Ile Glu Lys Thr Asp Pro Trp Phe Ala His Arg Thr 765 770 775cct atg cct aaa ata caa aat gtc tcc tct agt gat ttg ttg atg ctc 2586Pro Met Pro Lys Ile Gln Asn Val Ser Ser Ser Asp Leu Leu Met Leu 780 785 790ttg cga cag agt cct act cca cat ggg cta tcc tta tct gat ctc caa 2634Leu Arg Gln Ser Pro Thr Pro His Gly Leu Ser Leu Ser Asp Leu Gln 795 800 805gaa gcc aaa tat gag act ttt tct gat gat cca tca cct gga gca ata 2682Glu Ala Lys Tyr Glu Thr Phe Ser Asp Asp Pro Ser Pro Gly Ala Ile810 815 820 825gac agt aat aac agc ctg tct gaa atg aca cac ttc agg cca cag ctc 2730Asp Ser Asn Asn Ser Leu Ser Glu Met Thr His Phe Arg Pro Gln Leu 830 835 840cat cac agt ggg gac atg gta ttt acc cct gag tca ggc ctc caa tta 2778His His Ser Gly Asp Met Val Phe Thr Pro Glu Ser Gly Leu Gln Leu 845 850 855aga tta aat gag aaa ctg ggg aca act gca gca aca gag ttg aag aaa 2826Arg Leu Asn Glu Lys Leu Gly Thr Thr Ala Ala Thr Glu Leu Lys Lys 860 865 870ctt gat ttc aaa gtt tct agt aca tca aat aat ctg att tca aca att 2874Leu Asp Phe Lys Val Ser Ser Thr Ser Asn Asn Leu Ile Ser Thr Ile 875 880 885cca tca gac aat ttg gca gca ggt act gat aat aca agt tcc tta gga 2922Pro Ser Asp Asn Leu Ala Ala Gly Thr Asp Asn Thr Ser Ser Leu Gly890 895 900 905ccc cca agt atg cca gtt cat tat gat agt caa tta gat acc act cta 2970Pro Pro Ser Met Pro Val His Tyr Asp Ser Gln Leu Asp Thr Thr Leu 910 915 920ttt ggc aaa aag tca tct ccc ctt act gag tct ggt gga cct ctg agc 3018Phe Gly Lys Lys Ser Ser Pro Leu Thr Glu Ser Gly Gly Pro Leu Ser 925 930 935ttg agt gaa gaa aat aat gat tca aag ttg tta gaa tca ggt tta atg 3066Leu Ser Glu Glu Asn Asn Asp Ser Lys Leu Leu Glu Ser Gly Leu Met 940 945 950aat agc caa gaa agt tca tgg gga aaa aat gta tcg tca aca gag agt 3114Asn Ser Gln Glu Ser Ser Trp Gly Lys Asn Val Ser Ser Thr Glu Ser 955 960 965ggt agg tta ttt aaa ggg aaa aga gct cat gga cct gct ttg ttg act 3162Gly Arg Leu Phe Lys Gly Lys Arg Ala His Gly Pro Ala Leu Leu Thr970 975 980 985aaa gat aat gcc tta ttc aaa gtt agc atc tct ttg tta aag aca aac 3210Lys Asp Asn Ala Leu Phe Lys Val Ser Ile Ser Leu Leu Lys Thr Asn 990 995 1000aaa act tcc aat aat tca gca act aat aga aag act cac att gat ggc 3258Lys Thr Ser Asn Asn Ser Ala Thr Asn Arg Lys Thr His Ile Asp Gly 1005 1010 1015cca tca tta tta att gag aat agt cca tca gtc tgg caa aat ata tta 3306Pro Ser Leu Leu Ile Glu Asn Ser Pro Ser Val Trp Gln Asn Ile Leu 1020 1025 1030gaa agt gac act gag ttt aaa aaa gtg aca cct ttg att cat gac aga 3354Glu Ser Asp Thr Glu Phe Lys Lys Val Thr Pro Leu Ile His Asp Arg 1035 1040 1045atg ctt atg gac aaa aat gct aca gct ttg agg cta aat cat atg tca 3402Met Leu Met Asp Lys Asn Ala Thr Ala Leu Arg Leu Asn His Met Ser1050 1055 1060 1065aat aaa act act tca tca aaa aac atg gaa atg gtc caa cag aaa aaa 3450Asn Lys Thr Thr Ser Ser Lys Asn Met Glu Met Val Gln Gln Lys Lys 1070 1075 1080gag ggc ccc att cca cca gat gca caa aat cca gat atg tcg ttc ttt 3498Glu Gly Pro Ile Pro Pro Asp Ala Gln Asn Pro Asp Met Ser Phe Phe 1085 1090 1095aag atg cta ttc ttg cca gaa tca gca agg tgg ata caa agg act cat 3546Lys Met Leu Phe Leu Pro Glu Ser Ala Arg Trp Ile Gln Arg Thr His 1100 1105 1110gga aag aac tct ctg aac tct ggg caa ggc ccc agt cca aag caa tta 3594Gly Lys Asn Ser Leu Asn Ser Gly Gln Gly Pro Ser Pro Lys Gln Leu 1115 1120 1125gta tcc tta gga cca gaa aaa tct gtg gaa ggt cag aat ttc ttg tct 3642Val Ser Leu Gly Pro Glu Lys Ser Val Glu Gly Gln Asn Phe Leu Ser1130 1135 1140 1145gag aaa aac aaa gtg gta gta gga aag ggt gaa ttt aca aag gac gta 3690Glu Lys Asn Lys Val Val Val Gly Lys Gly Glu Phe Thr Lys Asp Val 1150 1155 1160gga ctc aaa gag atg gtt ttt cca agc agc aga aac cta ttt ctt act 3738Gly Leu Lys Glu Met Val Phe Pro Ser Ser Arg Asn Leu Phe Leu Thr 1165 1170 1175aac ttg gat aat tta cat gaa aat aat aca cac aat caa gaa aaa aaa 3786Asn Leu Asp Asn Leu His Glu Asn Asn Thr His Asn Gln Glu Lys Lys 1180 1185 1190att cag gaa gaa ata gaa aag aag gaa aca tta atc caa gag aat gta 3834Ile Gln Glu Glu Ile Glu Lys Lys Glu Thr Leu Ile Gln Glu Asn Val 1195 1200 1205gtt ttg cct cag ata cat aca gtg act ggc act aag aat ttc atg aag 3882Val Leu Pro Gln Ile His Thr Val Thr Gly Thr Lys Asn Phe Met Lys1210 1215 1220 1225aac ctt ttc tta ctg agc act agg caa aat gta gaa ggt tca tat gag 3930Asn Leu Phe Leu Leu Ser Thr Arg Gln Asn Val Glu Gly Ser Tyr Glu 1230 1235 1240ggg gca tat gct cca gta ctt caa gat ttt agg tca tta aat gat tca 3978Gly Ala Tyr Ala Pro Val Leu Gln Asp Phe Arg Ser Leu Asn Asp Ser 1245 1250 1255aca aat aga aca aag aaa cac aca gct cat ttc tca aaa aaa ggg gag 4026Thr Asn Arg Thr Lys Lys His Thr Ala His Phe Ser Lys Lys Gly Glu 1260 1265 1270gaa gaa aac ttg gaa ggc ttg gga aat caa acc aag caa att gta gag 4074Glu Glu Asn Leu Glu Gly Leu Gly Asn Gln Thr Lys Gln Ile Val Glu 1275 1280 1285aaa tat gca tgc acc aca agg ata tct cct aat aca agc cag cag aat 4122Lys Tyr Ala Cys Thr Thr Arg Ile Ser Pro Asn Thr Ser Gln Gln Asn1290 1295 1300 1305ttt gtc acg caa cgt agt aag aga gct ttg aaa caa ttc aga ctc cca 4170Phe Val Thr Gln Arg Ser Lys Arg Ala Leu Lys Gln Phe Arg Leu Pro 1310 1315 1320cta gaa gaa aca gaa ctt gaa aaa agg ata att gtg gat gac acc tca 4218Leu Glu Glu Thr Glu Leu Glu Lys Arg Ile Ile Val Asp Asp Thr Ser 1325 1330 1335acc cag tgg tcc aaa aac atg aaa cat ttg acc ccg agc acc ctc aca 4266Thr Gln Trp Ser Lys Asn Met Lys His Leu Thr Pro Ser Thr Leu Thr 1340 1345 1350cag ata gac tac aat gag aag gag aaa ggg gcc att act cag tct ccc 4314Gln Ile Asp Tyr Asn Glu Lys Glu Lys Gly Ala Ile Thr Gln Ser Pro 1355 1360 1365tta tca gat tgc ctt acg agg agt cat agc atc cct caa gca aat aga 4362Leu Ser Asp Cys Leu Thr Arg Ser His Ser Ile Pro Gln Ala Asn Arg1370 1375 1380 1385tct cca tta ccc att gca aag gta tca tca ttt cca tct att aga cct 4410Ser Pro Leu Pro Ile Ala Lys Val Ser Ser Phe Pro Ser Ile Arg Pro 1390 1395 1400ata tat ctg acc agg gtc cta ttc caa gac aac tct tct cat ctt cca 4458Ile Tyr Leu Thr Arg Val Leu Phe Gln Asp Asn Ser Ser His Leu Pro 1405 1410 1415gca gca tct tat aga aag aaa gat tct ggg gtc caa gaa agc agt cat 4506Ala Ala Ser Tyr Arg Lys Lys Asp Ser Gly Val Gln Glu Ser Ser His 1420 1425 1430ttc tta caa gga gcc aaa aaa aat aac ctt tct tta gcc att cta acc 4554Phe Leu Gln Gly Ala Lys Lys Asn Asn Leu Ser Leu Ala Ile Leu Thr 1435 1440 1445ttg gag atg act ggt gat caa aga gag gtt ggc tcc ctg ggg aca agt 4602Leu Glu Met Thr Gly Asp Gln Arg Glu Val Gly Ser Leu Gly Thr Ser1450 1455 1460 1465gcc aca aat tca gtc aca tac aag aaa gtt gag aac act gtt ctc ccg 4650Ala Thr Asn Ser Val Thr Tyr Lys Lys Val Glu Asn Thr Val Leu Pro 1470 1475 1480aaa cca gac ttg ccc aaa aca tct ggc aaa gtt gaa ttg ctt cca aaa 4698Lys Pro Asp Leu Pro Lys Thr Ser Gly Lys Val Glu Leu Leu Pro Lys 1485 1490 1495gtt cac att tat cag aag gac cta ttc cct acg gaa act agc aat ggg 4746Val His Ile Tyr Gln Lys Asp Leu Phe Pro Thr Glu Thr Ser Asn Gly 1500 1505 1510tct cct ggc cat ctg gat ctc gtg gaa ggg agc ctt ctt cag gga aca 4794Ser Pro Gly His Leu Asp Leu Val Glu Gly Ser Leu Leu Gln Gly Thr 1515 1520 1525gag gga gcg att aag tgg aat gaa gca aac aga cct gga aaa gtt ccc 4842Glu Gly Ala Ile Lys Trp Asn Glu Ala Asn Arg Pro Gly Lys Val Pro1530 1535 1540 1545ttt ctg aga gta gca aca gaa agc tct gca aag act ccc tcc aag cta 4890Phe Leu Arg Val Ala Thr Glu Ser Ser Ala Lys Thr Pro Ser Lys Leu 1550 1555 1560ttg gat cct ctt gct tgg gat aac cac tat ggt act cag ata cca aaa 4938Leu Asp Pro Leu Ala Trp Asp Asn His Tyr Gly Thr Gln Ile Pro Lys 1565 1570 1575gaa gag tgg aaa tcc caa gag aag tca cca gaa aaa aca gct ttt aag 4986Glu Glu Trp Lys Ser Gln Glu Lys Ser Pro Glu Lys Thr Ala Phe Lys 1580 1585 1590aaa aag gat acc att ttg tcc ctg aac gct tgt gaa agc aat cat gca 5034Lys Lys Asp Thr Ile Leu Ser Leu Asn Ala Cys Glu Ser Asn His Ala 1595 1600 1605ata gca gca ata aat gag gga caa aat aag ccc gaa ata gaa gtc acc 5082Ile Ala Ala Ile Asn Glu Gly Gln Asn Lys Pro Glu Ile Glu Val Thr1610 1615 1620 1625tgg gca aag caa ggt agg act gaa agg ctg tgc tct caa aac cca cca 5130Trp Ala Lys Gln Gly Arg Thr Glu Arg Leu Cys Ser Gln Asn Pro Pro 1630 1635 1640gtc ttg aaa cgc cat caa cgg gaa ata act cgt act act ctt cag tca 5178Val Leu Lys Arg His Gln Arg Glu Ile Thr Arg Thr Thr Leu Gln Ser 1645 1650 1655gat caa gag gaa att gac tat gat gat acc ata tca gtt gaa atg aag 5226Asp Gln Glu Glu Ile Asp Tyr Asp Asp Thr Ile Ser Val Glu Met Lys 1660 1665 1670aag gaa gat ttt gac att tat gat gag gat gaa aat cag agc ccc cgc 5274Lys Glu Asp Phe Asp Ile Tyr Asp Glu Asp Glu Asn Gln Ser Pro Arg 1675 1680 1685agc ttt caa aag aaa aca cga cac tat ttt att gct gca gtg gag agg 5322Ser Phe Gln Lys Lys Thr Arg His Tyr Phe Ile Ala Ala Val Glu Arg1690 1695 1700 1705ctc tgg gat tat ggg atg agt agc tcc cca cat gtt cta aga aac agg 5370Leu Trp Asp Tyr Gly Met Ser Ser Ser Pro His Val Leu Arg Asn Arg 1710 1715 1720gct cag agt ggc agt gtc cct cag ttc aag aaa gtt gtt ttc cag gaa 5418Ala Gln Ser Gly Ser Val Pro Gln Phe Lys Lys Val Val Phe Gln Glu 1725 1730 1735ttt act gat ggc tcc ttt act cag ccc tta tac cgt gga gaa cta aat 5466Phe Thr Asp Gly Ser Phe Thr Gln Pro Leu Tyr Arg Gly Glu Leu Asn 1740 1745 1750gaa cat ttg gga ctc ctg ggg cca tat ata aga gca gaa gtt gaa gat 5514Glu His Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp 1755 1760 1765aat atc atg gta act ttc aga aat cag gcc tct cgt ccc tat tcc ttc 5562Asn Ile Met Val Thr Phe Arg Asn Gln Ala Ser Arg Pro Tyr Ser Phe1770 1775 1780 1785tat tct agc ctt att tct tat gag gaa gat cag agg caa gga gca gaa 5610Tyr Ser Ser Leu Ile Ser Tyr Glu Glu Asp Gln Arg Gln Gly Ala Glu 1790 1795 1800cct aga aaa aac ttt gtc aag cct aat gaa acc aaa act tac ttt tgg 5658Pro Arg Lys Asn Phe Val Lys Pro Asn Glu Thr Lys Thr Tyr Phe Trp 1805 1810 1815aaa gtg caa cat cat atg gca ccc act aaa gat gag ttt gac tgc aaa 5706Lys Val Gln His His Met Ala Pro Thr Lys Asp Glu Phe Asp Cys Lys 1820 1825 1830gcc tgg gct tat ttc tct gat gtt gac ctg gaa aaa gat gtg cac tca 5754Ala Trp Ala Tyr Phe Ser Asp Val Asp Leu Glu Lys Asp Val His Ser 1835 1840 1845ggc ctg att gga ccc ctt ctg gtc tgc cac act aac aca ctg aac cct 5802Gly Leu Ile Gly Pro Leu Leu Val Cys His Thr Asn Thr Leu Asn Pro1850 1855 1860 1865gct cat ggg aga caa gtg aca gta cag gaa ttt gct ctg ttt ttc acc 5850Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe Phe Thr 1870 1875 1880atc ttt gat gag acc aaa agc tgg tac ttc act gaa aat atg gaa aga 5898Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn Met Glu Arg 1885 1890 1895aac tgc agg gct ccc tgc aat atc cag atg gaa gat ccc act ttt aaa 5946Asn Cys Arg Ala Pro Cys Asn Ile Gln Met Glu Asp Pro Thr Phe Lys 1900 1905 1910gag aat tat cgc ttc cat gca atc aat ggc tac ata atg gat aca cta 5994Glu Asn Tyr Arg Phe His Ala Ile Asn Gly Tyr Ile Met Asp Thr Leu 1915 1920 1925cct ggc tta gta atg gct cag gat caa agg att cga tgg tat ctg ctc 6042Pro Gly Leu Val Met Ala Gln Asp Gln Arg Ile Arg Trp Tyr Leu Leu1930 1935 1940 1945agc atg ggc agc aat gaa aac atc cat tct att cat ttc agt gga cat 6090Ser Met Gly Ser Asn Glu Asn Ile His Ser Ile His Phe Ser Gly His 1950 1955 1960gtg ttc act gta cga aaa aaa gag gag tat aaa atg gca ctg tac aat 6138Val Phe Thr Val Arg Lys Lys Glu Glu Tyr Lys Met Ala Leu Tyr Asn 1965 1970 1975ctc tat cca ggt gtt ttt gag aca gtg gaa atg tta cca tcc aaa gct 6186Leu Tyr Pro Gly Val Phe Glu Thr Val Glu Met Leu Pro Ser Lys Ala 1980 1985 1990gga att tgg cgg gtg gaa tgc ctt att ggc gag cat cta cat gct ggg 6234Gly Ile Trp Arg Val Glu Cys Leu Ile Gly Glu His Leu His Ala Gly 1995 2000 2005atg agc aca ctt ttt ctg gtg tac agc aat aag tgt cag act ccc ctg 6282Met Ser Thr Leu Phe Leu Val Tyr Ser Asn Lys Cys Gln Thr Pro Leu2010 2015 2020 2025gga atg gct tct gga cac att aga gat ttt cag att aca gct tca gga 6330Gly Met Ala Ser Gly His Ile Arg Asp Phe Gln Ile Thr Ala Ser Gly 2030 2035 2040caa tat gga cag tgg gcc cca aag ctg gcc aga ctt cat tat tcc gga 6378Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu His Tyr Ser Gly 2045 2050 2055tca atc aat gcc tgg agc acc aag gag ccc ttt tct tgg atc aag gtg 6426Ser Ile Asn Ala Trp Ser Thr Lys Glu Pro Phe Ser Trp Ile Lys Val 2060 2065 2070gat ctg ttg gca cca atg att att cac ggc atc aag acc cag ggt gcc 6474Asp Leu Leu Ala Pro Met Ile Ile His Gly Ile Lys Thr Gln Gly Ala 2075 2080 2085cgt cag aag ttc tcc agc ctc tac atc tct cag ttt atc atc atg tat 6522Arg Gln Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr2090 2095 2100 2105agt ctt gat ggg aag aag tgg cag act tat cga gga aat tcc act gga 6570Ser Leu Asp Gly Lys Lys Trp Gln Thr Tyr Arg Gly Asn Ser Thr Gly 2110 2115 2120acc tta atg gtc ttc ttt ggc aat gtg gat tca tct ggg ata aaa cac 6618Thr Leu Met Val Phe Phe Gly Asn Val Asp Ser Ser Gly Ile Lys His 2125 2130 2135aat att ttt aac cct cca att att gct cga tac atc cgt ttg cac cca 6666Asn Ile Phe Asn Pro Pro Ile Ile Ala Arg Tyr Ile Arg Leu His Pro 2140 2145 2150act cat tat agc att cgc agc act ctt cgc atg gag ttg atg ggc tgt 6714Thr His Tyr Ser Ile Arg Ser Thr Leu Arg Met Glu Leu Met Gly Cys 2155 2160 2165gat tta aat agt tgc agc atg cca ttg gga atg gag agt aaa gca ata 6762Asp Leu Asn Ser Cys Ser Met Pro Leu Gly Met Glu Ser Lys Ala Ile2170 2175 2180 2185tca gat gca cag att act gct tca tcc tac ttt acc aat atg ttt gcc 6810Ser Asp Ala Gln Ile Thr Ala Ser Ser Tyr Phe Thr Asn Met Phe Ala 2190 2195 2200acc tgg tct cct tca aaa gct cga ctt cac ctc caa ggg agg agt aat 6858Thr Trp Ser Pro Ser Lys Ala Arg Leu His Leu Gln Gly Arg Ser Asn 2205 2210 2215gcc tgg aga cct cag gtg aat aat cca aaa gag tgg ctg caa gtg gac 6906Ala Trp Arg Pro Gln Val Asn Asn Pro Lys Glu Trp Leu Gln Val Asp 2220 2225 2230ttc cag aag aca atg aaa gtc aca gga gta act act cag gga gta aaa 6954Phe Gln Lys Thr Met Lys Val Thr Gly Val Thr Thr Gln Gly Val Lys 2235 2240 2245tct ctg ctt acc agc atg tat gtg aag gag ttc ctc atc tcc agc agt 7002Ser Leu Leu Thr Ser Met Tyr Val Lys Glu Phe Leu Ile Ser Ser Ser2250 2255 2260 2265caa gat ggc cat cag tgg act ctc ttt ttt cag aat ggc aaa gta aag 7050Gln Asp Gly His Gln Trp Thr Leu Phe Phe Gln Asn Gly Lys Val Lys 2270 2275 2280gtt ttt cag gga aat caa gac tcc ttc aca cct gtg gtg aac tct cta 7098Val Phe Gln Gly Asn Gln Asp Ser Phe Thr Pro Val Val Asn Ser Leu 2285 2290 2295gac cca ccg tta ctg act cgc tac ctt cga att cac ccc cag agt tgg 7146Asp Pro Pro Leu Leu Thr Arg Tyr Leu Arg Ile His Pro Gln Ser Trp 2300 2305 2310gtg cac cag att gcc ctg agg atg gag gtt ctg ggc tgc gag gca cag 7194Val His Gln Ile Ala Leu Arg Met Glu Val Leu Gly Cys Glu Ala Gln 2315 2320 2325gac ctc tac tgagggtggc cactgcagca cctgccactg ccgtcacctc 7243Asp Leu Tyr2330tccctcctca gctccagggc agtgtccctc cctggcttgc cttctacctt tgtgctaaat 7303cctagcagac actgccttga agcctcctga attaactatc atcagtcctg catttctttg 7363gtggggggcc aggagggtgc atccaattta acttaactct tacctatttt ctgcagctgc 7423tcccagatta ctccttcctt ccaatataac taggcaaaaa gaagtgagga gaaacctgca 7483tgaaagcatt cttccctgaa aagttaggcc tctcagagtc accacttcct ctgttgtaga 7543aaaactatgt gatgaaactt tgaaaaagat atttatgatg ttaacatttc aggttaagcc 7603tcatacgttt aaaataaaac tctcagttgt ttattatcct gatcaagcat ggaacaaagc 7663atgtttcagg atcagatcaa tacaatcttg gagtcaaaag gcaaatcatt tggacaatct 7723gcaaaatgga gagaatacaa taactactac agtaaagtct gtttctgctt ccttacacat 7783agatataatt atgttattta gtcattatga ggggcacatt cttatctcca aaactagcat 7843tcttaaactg agaattatag atggggttca agaatcccta agtcccctga aattatataa 7903ggcattctgt ataaatgcaa atgtgcattt ttctgacgag tgtccataga tataaagcca 7963ttggtcttaa ttctgaccaa taaaaaaata agtcaggagg atgcaattgt tgaaagcttt 8023gaaataaaat aacatgtctt cttgaaattt gtgatggcca agaaagaaaa tgatgatgac 8083attaggcttc taaaggacat acatttaata tttctgtgga aatatgagga aaatccatgg 8143ttatctgaga taggagatac aaactttgta attctaataa tgcactcagt ttactctctc 8203cctctactaa tttcctgctg aaaataacac aacaaaaatg taacagggga aattatatac 8263cgtgactgaa aactagagtc ctacttacat agttgaaata tcaaggaggt cagaagaaaa 8323ttggactggt gaaaacagaa aaaacactcc agtctgccat atcaccacac aataggatcc 8383cccttcttgc cctccacccc cataagattg tgaagggttt actgctcctt ccatctgcct 8443gcaccccttc actatgacta cacagaactc tcctgatagt aaagggggct ggaggcaagg 8503ataagttata gagcagttgg aggaagcatc caaagactgc aacccagggc aaatggaaaa 8563caggagatcc taatatgaaa gaaaaatgga tcccaatctg agaaaaggca aaagaatggc 8623tacttttttc tatgctggag tattttctaa taatcctgct tgacccttat ctgacctctt 8683tggaaactat aacatagctg tcacagtata gtcacaatcc acaaatgatg caggtgcaaa 8743tggtttatag ccctgtgaag ttcttaaagt ttagaggcta acttacagaa atgaataagt 8803tgttttgttt tatagcccgg tagaggagtt aaccccaaag gtgatatggt tttatttcct 8863gttatgttta acttgataat cttattttgg cattcttttc ccattgacta tatacatctc 8923tatttctcaa atgttcatgg aactagctct tttattttcc tgctggtttc ttcagtaatg 8983agttaaataa aacattgaca cataca 9009 2 2332 PRT Homo sapiens 2Ala Thr Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser Trp Asp Tyr 1 5 10 15Met Gln Ser Asp Leu Gly Glu Leu Pro Val Asp Ala Arg Phe Pro Pro 20 25 30Arg Val Pro Lys Ser Phe Pro Phe Asn Thr Ser Val Val Tyr Lys Lys 35 40 45Thr Leu Phe Val Glu Phe Thr Val His Leu Phe Asn Ile Ala Lys Pro 50 55 60Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile Gln Ala Glu Val 65 70 75 80Tyr Asp Thr Val Val Ile Thr Leu Lys Asn Met Ala Ser His Pro Val 85 90 95Ser Leu His Ala Val Gly Val Ser Tyr Trp Lys Ala Ser Glu Gly Ala 100 105 110Glu Tyr Asp Asp Gln Thr Ser Gln Arg Glu Lys Glu Asp Asp Lys Val 115 120 125Phe Pro Gly Gly Ser His Thr Tyr Val Trp Gln Val Leu Lys Glu Asn 130 135 140Gly Pro Met Ala Ser Asp Pro Leu Cys Leu Thr Tyr Ser Tyr Leu Ser145 150 155 160His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu Ile Gly Ala Leu 165 170 175Leu Val Cys Arg Glu Gly Ser Leu Ala Lys Glu Lys Thr Gln Thr Leu 180 185 190His Lys Phe Ile Leu Leu Phe Ala Val Phe Asp Glu Gly Lys Ser Trp 195 200 205His Ser Glu Thr Lys Asn Ser Leu Met Gln Asp Arg Asp Ala Ala Ser 210 215 220Ala Arg Ala Trp Pro Lys Met His Thr Val Asn Gly Tyr Val Asn Arg225 230 235 240Ser Leu Pro Gly Leu Ile Gly Cys His Arg Lys Ser Val Tyr Trp His 245 250 255Val Ile Gly Met Gly Thr Thr Pro Glu Val His Ser Ile Phe Leu Glu 260 265 270Gly His Thr Phe Leu Val Arg Asn His Arg Gln Ala Ser Leu Glu Ile 275 280 285Ser Pro Ile Thr Phe Leu Thr Ala Gln Thr Leu Leu Met Asp Leu Gly 290 295 300Gln Phe Leu Leu Phe Cys His Ile Ser Ser His Gln His Asp Gly Met305 310 315 320Glu Ala Tyr Val Lys Val Asp Ser Cys Pro Glu Glu Pro Gln Leu Arg 325 330 335Met Lys Asn Asn Glu Glu Ala Glu Asp Tyr Asp Asp Asp Leu Thr Asp 340 345 350Ser Glu Met Asp Val Val Arg Phe Asp Asp Asp Asn Ser Pro Ser Phe 355 360 365Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr Trp Val His 370 375 380Tyr Ile Ala Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro Leu Val Leu385 390 395 400Ala Pro Asp Asp Arg Ser Tyr Lys Ser Gln Tyr Leu Asn Asn Gly Pro 405 410 415Gln Arg Ile Gly Arg Lys Tyr Lys Lys Val Arg Phe Met Ala Tyr Thr 420 425 430Asp Glu Thr Phe Lys Thr Arg Glu Ala Ile Gln His Glu Ser Gly Ile 435 440 445Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu Leu Ile Ile 450 455 460Phe Lys Asn Gln Ala Ser Arg Pro Tyr Asn Ile Tyr Pro His Gly Ile465 470 475 480Thr Asp Val Arg Pro Leu Tyr Ser Arg Arg Leu Pro Lys Gly Val Lys 485 490 495His Leu Lys Asp Phe Pro Ile Leu Pro Gly Glu Ile Phe Lys Tyr Lys 500 505 510Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp Pro Arg Cys 515 520 525Leu Thr Arg Tyr Tyr Ser Ser Phe Val Asn Met Glu Arg Asp Leu Ala 530 535 540Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu Ser Val Asp545 550 555 560Gln Arg Gly Asn Gln Ile Met Ser Asp Lys Arg Asn Val Ile Leu Phe 565 570 575Ser Val Phe Asp Glu Asn Arg Ser Trp Tyr Leu Thr Glu Asn Ile Gln 580 585 590Arg Phe Leu Pro Asn Pro Ala Gly Val Gln Leu Glu Asp Pro Glu Phe 595 600 605Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val Phe Asp Ser 610 615 620Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp Tyr Ile Leu625 630 635 640Ser Ile Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe Ser Gly Tyr 645 650 655Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr Leu Phe Pro 660 665 670Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro Gly Leu Trp 675 680 685Ile Leu Gly Cys His Asn Ser Asp Phe Arg Asn Arg Gly Met Thr Ala 690 695 700Leu Leu Lys Val Ser Ser Cys Asp Lys Asn Thr Gly Asp Tyr Tyr Glu705 710 715 720Asp Ser Tyr Glu Asp Ile Ser Ala Tyr Leu Leu Ser Lys Asn Asn Ala 725 730 735Ile Glu Pro Arg Ser Phe Ser Gln Asn Ser Arg His Pro Ser Thr Arg 740 745 750Gln Lys Gln Phe Asn Ala Thr Thr Ile Pro Glu Asn Asp Ile Glu Lys 755 760 765Thr Asp Pro Trp Phe Ala His Arg Thr Pro Met Pro Lys Ile Gln Asn 770 775 780Val Ser Ser Ser Asp Leu Leu Met Leu Leu Arg Gln Ser Pro Thr Pro785 790 795 800His Gly Leu Ser Leu Ser Asp Leu Gln Glu Ala Lys Tyr Glu Thr Phe 805 810 815Ser Asp Asp Pro Ser Pro Gly Ala Ile Asp Ser Asn Asn Ser Leu Ser 820 825 830Glu Met Thr His Phe Arg Pro Gln Leu His His Ser Gly Asp Met Val 835 840 845Phe Thr Pro Glu Ser Gly Leu Gln Leu Arg Leu Asn Glu Lys Leu Gly 850 855 860Thr Thr Ala Ala Thr Glu Leu Lys Lys Leu Asp Phe Lys Val Ser Ser865 870 875 880Thr Ser Asn Asn Leu Ile Ser Thr Ile Pro Ser Asp Asn Leu Ala Ala 885 890 895Gly Thr Asp Asn Thr Ser Ser Leu Gly Pro Pro Ser Met Pro Val His 900 905 910Tyr Asp Ser Gln Leu Asp Thr Thr Leu Phe Gly Lys Lys Ser Ser Pro 915 920 925Leu Thr Glu Ser Gly Gly Pro Leu Ser Leu Ser Glu Glu Asn Asn Asp 930 935 940Ser Lys Leu Leu Glu Ser Gly Leu Met Asn Ser Gln Glu Ser Ser Trp945 950 955 960Gly Lys Asn Val Ser Ser Thr Glu Ser Gly Arg Leu Phe Lys Gly Lys 965 970 975Arg Ala His Gly Pro Ala Leu Leu Thr Lys Asp Asn Ala Leu Phe Lys 980 985 990Val Ser Ile Ser Leu Leu Lys Thr Asn Lys Thr Ser Asn Asn Ser Ala 995 1000 1005Thr Asn Arg Lys Thr His Ile Asp Gly Pro Ser Leu Leu Ile Glu Asn 1010 1015 1020Ser Pro Ser Val Trp Gln Asn Ile Leu Glu Ser Asp Thr Glu Phe Lys1025 1030 1035 1040Lys Val Thr Pro Leu Ile His Asp Arg Met Leu Met Asp Lys Asn Ala 1045 1050 1055Thr Ala Leu Arg Leu Asn His Met Ser Asn Lys Thr Thr Ser Ser Lys 1060 1065 1070Asn Met Glu Met Val Gln Gln Lys Lys Glu Gly Pro Ile Pro Pro Asp 1075 1080 1085Ala Gln Asn Pro Asp Met Ser Phe Phe Lys Met Leu Phe Leu Pro Glu 1090 1095 1100Ser Ala Arg Trp Ile Gln Arg Thr His Gly Lys Asn Ser Leu Asn Ser1105 1110 1115 1120Gly Gln Gly Pro Ser Pro Lys Gln Leu Val Ser Leu Gly Pro Glu Lys 1125 1130 1135Ser Val Glu Gly Gln Asn Phe Leu Ser Glu Lys Asn Lys Val Val Val 1140 1145 1150Gly Lys Gly Glu Phe Thr Lys Asp Val Gly Leu Lys Glu Met Val Phe 1155 1160 1165Pro Ser Ser Arg Asn Leu Phe Leu Thr Asn Leu Asp Asn Leu His Glu 1170 1175 1180Asn Asn Thr His Asn Gln Glu Lys Lys Ile Gln Glu Glu Ile Glu Lys1185 1190 1195 1200Lys Glu Thr Leu Ile Gln Glu Asn Val Val Leu Pro Gln Ile His Thr 1205 1210 1215Val Thr Gly Thr Lys Asn Phe Met Lys Asn Leu Phe Leu Leu Ser Thr 1220 1225 1230Arg Gln Asn Val Glu Gly Ser Tyr Glu Gly Ala Tyr Ala Pro Val Leu 1235 1240 1245Gln Asp Phe Arg Ser Leu Asn Asp Ser Thr Asn Arg Thr Lys Lys His 1250 1255 1260Thr Ala His Phe Ser Lys Lys Gly Glu Glu Glu Asn Leu Glu Gly Leu1265 1270 1275 1280Gly Asn Gln Thr Lys Gln Ile Val Glu Lys Tyr Ala Cys Thr Thr Arg 1285 1290 1295Ile Ser Pro Asn Thr Ser Gln Gln Asn Phe Val Thr Gln Arg Ser Lys 1300 1305 1310Arg Ala Leu Lys Gln Phe Arg Leu Pro Leu Glu Glu Thr Glu Leu Glu 1315 1320 1325Lys Arg Ile Ile Val Asp Asp Thr Ser Thr Gln Trp Ser Lys Asn Met 1330 1335 1340Lys His Leu Thr Pro Ser Thr Leu Thr Gln Ile Asp Tyr Asn Glu Lys1345 1350 1355 1360Glu Lys Gly Ala Ile Thr Gln Ser Pro Leu Ser Asp Cys Leu Thr Arg 1365 1370 1375Ser His Ser Ile Pro Gln Ala Asn Arg Ser Pro Leu Pro Ile Ala Lys 1380 1385 1390Val Ser Ser Phe Pro Ser Ile Arg Pro Ile Tyr Leu Thr Arg Val Leu 1395 1400 1405Phe Gln Asp Asn Ser Ser His Leu Pro Ala Ala Ser Tyr Arg Lys Lys 1410 1415 1420Asp Ser Gly Val Gln Glu Ser Ser His Phe Leu Gln Gly Ala Lys Lys1425 1430 1435 1440Asn Asn Leu Ser Leu Ala Ile Leu Thr Leu Glu Met Thr Gly Asp Gln 1445 1450 1455Arg Glu Val Gly Ser Leu Gly Thr Ser Ala Thr Asn Ser Val Thr Tyr 1460 1465 1470Lys Lys Val Glu Asn Thr Val Leu Pro Lys Pro Asp Leu Pro Lys Thr 1475 1480 1485Ser Gly Lys Val Glu Leu Leu Pro Lys Val His Ile Tyr Gln Lys Asp 1490 1495 1500Leu Phe Pro Thr Glu Thr Ser Asn Gly Ser Pro Gly His Leu Asp Leu1505 1510 1515 1520Val Glu Gly Ser Leu Leu Gln Gly Thr Glu Gly Ala Ile Lys Trp Asn 1525 1530 1535Glu Ala Asn Arg Pro Gly Lys Val Pro Phe Leu Arg Val Ala Thr Glu 1540 1545 1550Ser Ser Ala Lys Thr Pro Ser Lys Leu Leu Asp Pro Leu Ala Trp Asp 1555 1560 1565Asn His Tyr Gly Thr Gln Ile Pro Lys Glu Glu Trp Lys Ser Gln Glu 1570 1575 1580Lys Ser Pro Glu Lys Thr Ala Phe Lys Lys Lys Asp Thr Ile Leu Ser1585 1590 1595 1600Leu Asn Ala Cys Glu Ser Asn His Ala Ile Ala Ala Ile Asn Glu Gly 1605 1610 1615Gln Asn Lys Pro Glu Ile Glu Val Thr Trp Ala Lys Gln Gly Arg Thr 1620 1625 1630Glu Arg Leu Cys Ser Gln Asn Pro Pro Val Leu Lys Arg His Gln Arg 1635 1640 1645Glu Ile Thr Arg Thr Thr Leu Gln Ser Asp Gln Glu Glu Ile Asp Tyr 1650 1655 1660Asp Asp Thr Ile Ser Val Glu Met Lys Lys Glu Asp Phe Asp Ile Tyr1665 1670 1675 1680Asp Glu Asp Glu Asn Gln Ser Pro Arg Ser Phe Gln Lys Lys Thr Arg 1685 1690 1695His Tyr Phe Ile Ala Ala Val Glu Arg Leu Trp Asp Tyr Gly Met Ser 1700 1705 1710Ser Ser Pro His Val Leu Arg Asn Arg Ala Gln Ser Gly Ser Val Pro 1715 1720 1725Gln Phe Lys Lys Val Val Phe Gln Glu Phe Thr Asp Gly Ser Phe Thr 1730 1735 1740Gln Pro Leu Tyr Arg Gly Glu Leu Asn Glu His Leu Gly Leu Leu Gly1745 1750 1755 1760Pro Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe Arg 1765 1770 1775Asn Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu Ile Ser Tyr 1780 1785 1790Glu Glu Asp Gln Arg Gln Gly Ala Glu Pro Arg Lys Asn Phe Val Lys 1795 1800 1805Pro Asn Glu Thr Lys Thr Tyr Phe Trp Lys Val Gln His His Met Ala 1810 1815 1820Pro Thr Lys Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr Phe Ser Asp1825 1830 1835 1840Val Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile Gly Pro Leu Leu 1845 1850 1855Val Cys His Thr Asn Thr Leu Asn Pro Ala His Gly Arg Gln Val Thr 1860 1865 1870Val Gln Glu Phe Ala Leu Phe Phe Thr Ile Phe Asp Glu Thr Lys Ser 1875 1880 1885Trp Tyr Phe Thr Glu Asn Met Glu Arg Asn Cys Arg Ala Pro Cys Asn 1890 1895 1900Ile Gln Met Glu Asp Pro Thr Phe Lys Glu Asn Tyr Arg Phe His Ala1905 1910 1915 1920Ile Asn Gly Tyr Ile Met Asp Thr Leu Pro Gly Leu Val Met Ala Gln 1925 1930 1935Asp Gln Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Ser Asn Glu Asn 1940 1945 1950Ile His Ser Ile His Phe Ser Gly His Val Phe Thr Val Arg Lys Lys 1955 1960 1965Glu Glu Tyr Lys Met Ala Leu Tyr Asn Leu Tyr Pro Gly Val Phe Glu 1970 1975 1980Thr Val Glu Met Leu Pro Ser Lys Ala Gly Ile Trp Arg Val Glu Cys1985 1990 1995 2000Leu Ile Gly Glu His Leu His Ala Gly Met Ser Thr Leu Phe Leu Val 2005 2010 2015Tyr Ser Asn Lys Cys Gln Thr Pro Leu Gly Met Ala Ser Gly His Ile 2020 2025 2030Arg Asp Phe Gln Ile Thr Ala Ser Gly Gln Tyr Gly Gln Trp Ala Pro 2035 2040 2045Lys Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr 2050 2055 2060Lys Glu Pro Phe Ser Trp Ile Lys Val Asp Leu Leu Ala Pro Met Ile2065 2070 2075 2080Ile His Gly Ile Lys Thr Gln Gly Ala Arg Gln Lys Phe Ser Ser Leu 2085 2090 2095Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly Lys Lys Trp 2100 2105 2110Gln Thr Tyr Arg Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly 2115 2120 2125Asn Val Asp Ser Ser Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile 2130 2135 2140Ile Ala Arg Tyr Ile Arg Leu His Pro Thr His Tyr Ser Ile Arg Ser2145 2150 2155 2160Thr Leu Arg Met Glu Leu Met Gly Cys Asp Leu Asn Ser Cys Ser Met 2165 2170 2175Pro Leu Gly Met Glu Ser Lys Ala Ile Ser Asp Ala Gln Ile Thr Ala 2180 2185 2190Ser Ser Tyr Phe Thr Asn Met Phe Ala Thr Trp Ser Pro Ser Lys Ala 2195 2200 2205Arg Leu His Leu Gln Gly Arg Ser Asn Ala Trp Arg Pro Gln Val Asn 2210 2215 2220Asn Pro Lys Glu Trp Leu Gln Val Asp Phe Gln Lys Thr Met Lys Val2225 2230 2235 2240Thr Gly Val Thr Thr Gln Gly Val Lys Ser Leu Leu Thr Ser Met Tyr 2245 2250 2255Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly His Gln Trp Thr 2260 2265 2270Leu Phe Phe Gln Asn Gly Lys Val Lys Val Phe Gln Gly Asn Gln Asp 2275 2280 2285Ser Phe Thr Pro Val Val Asn Ser Leu Asp Pro Pro Leu Leu Thr Arg 2290 2295 2300Tyr Leu Arg Ile His Pro Gln Ser Trp Val His Gln Ile Ala Leu Arg2305 2310 2315 2320Met Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 2325 2330 3 24 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 3gtggattcat ctgggataaa acac 24 4 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 4aggagaccag gtggcaaaga tattggtaaa gtaggatga 39 5 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 5tgaaggagac caggtggcca acatattggt aaagtagga 39 6 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 6ccactctttt ggattattgg cctgaggtct ccaggcatt 39 7 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 7gtccacttgc agccactcct ctggattatt cacctgagg 39 8 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 8cttcacatac atgctggtga acagagattt tactccctg 39 9 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 9aggagaccag gtggccaaga tattggtaaa gtaggatga 39 10 45 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 10cacttgcagc cactcctctg gattattggc ctgaggtctc caggc 45 11 21 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 11agtttttcta caacagagga a 21 12 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 12tcatcctact ttaccaatat ctttgccacc tggtctcct 39 13 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 13tcctacttta ccaatatgtt ggccacctgg tctccttca 39 14 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 14aatgcctgga gacctcaggc caataatcca aaagagtgg 39 15 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 15cctcaggtga ataatccaga ggagtggctg caagtggac 39 16 39 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 16cagggagtaa aatctctgtt caccagcatg tatgtgaag 39 17 39 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 17tcatcctact ttaccaatat cttggccacc tggtctcct 39 18 45 DNA Artificial Sequence Description of Artificial Sequence Oligonucleotide primer 18gcctggagac ctcaggccaa taatccagag gagtggctgc aagtg 45 19 160 PRT Porcine 19Ser Cys Ser Met Pro Leu Gly Met Gln Asn Lys Ala Ile Ser Asp Ser 1 5 10 15Gln Ile Thr Ala Ser Ser His Leu Ser Asn Ile Phe Ala Thr Trp Ser 20 25 30Pro Ser Gln Ala Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg 35 40 45Pro Arg Val Ser Ser Ala Glu Glu Trp Leu Gln Val Asp Leu Gln Lys 50 55 60Thr Val Lys Val Thr Gly Ile Thr Thr Gln Gly Val Lys Ser Leu Leu 65 70 75 80Ser Ser Met Tyr Val Lys Glu Phe Leu Val Ser Ser Ser Gln Asp Gly 85 90 95Arg Arg Trp Thr Leu Phe Leu Gln Asp Gly His Thr Lys Val Phe Gln 100 105 110Gly Asn Gln Asp Ser Ser Thr Pro Val Val Asn Ala Leu Asp Pro Pro 115 120 125Leu Phe Thr Arg Tyr Leu Arg Ile His Pro Thr Ser Trp Ala Gln His 130 135 140Ile Ala Leu Arg Leu Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr145 150 155 160 20 160 PRT murine 20Ser Cys Ser Ile Pro Leu Gly Met Glu Ser Lys Val Ile Ser Asp Thr 1 5 10 15Gln Ile Thr Ala Ser Ser Tyr Phe Thr Asn Met Phe Ala Thr Trp Ser 20 25 30Pro Ser Gln Ala Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg 35 40 45Pro Gln Val Asn Asp Pro Lys Gln Trp Leu Gln Val Asp Leu Gln Lys 50 55 60Thr Met Lys Val Thr Gly Ile Ile Thr Gln Gly Val Lys Ser Leu Phe 65 70 75 80Thr Ser Met Phe Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly 85 90 95His His Trp Thr Gln Ile Leu Tyr Asn Gly Lys Val Lys Val Phe Gln 100 105 110Gly Asn Gln Asp Ser Ser Thr Pro Met Met Asn Ser Leu Asp Pro Pro 115 120 125Leu Leu Thr Arg Tyr Leu Arg Ile His Pro Gln Ile Trp Glu His Gln 130 135 140Ile Ala Leu Arg Leu Glu Ile Leu Gly Cys Glu Ala Gln Gln Gln Tyr145 150 155 160 21 160 PRT canine 21Ser Cys Ser Met Pro Leu Gly Met Glu Ser Lys Ala Ile Ser Asp Ala 1 5 10 15Gln Ile Thr Ala Ser Ser Tyr Leu Ser Ser Met Leu Ala Thr Trp Ser 20 25 30Pro Ser Gln Ala Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg 35 40 45Pro Gln Ala Asn Asn Pro Lys Glu Trp Leu Gln Val Asp Phe Arg Lys 50 55 60Thr Met Lys Val Thr Gly Ile Thr Thr Gln Gly Val Lys Ser Leu Leu 65 70 75 80Ile Ser Met Tyr Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly 85 90 95His Asn Gln Thr Leu Phe Leu Gln Asn Gly Lys Val Lys Val Phe Gln 100 105 110Gly Asn Arg Asp Ser Ser Thr Pro Val Arg Asn Arg Leu Glu Pro Pro 115 120 125Leu Val Ala Arg Tyr Val Arg Leu His Pro Gln Ser Trp Ala His His 130 135 140Ile Ala Leu Arg Leu Glu Val Leu Gly Cys Asp Thr Gln Gln Pro Ala145 150 155 160

Claims

1. A modified human factor VIII comprising at least one amino acid substitution in the C2 domain wherein the substitution is limited to at least one position selected from the group consisting of 2199, 2200, 2223, 2227, 2251, and 2252 corresponding to SEQ ID NO:2, wherein the modified factor VIII has reduced immunogenicity and/or antigenicity compared to the corresponding human factor VIII protein.

2. The modified human factor VIII of claim 1 lacking a B-domain.

3. The modified human factor VIII of claim 1 wherein one of the substitution is isoleucine substituted for methionine 2199 corresponding to SEQ ID NO:2.

4. The modified human factor VIII of claim 1 wherein one of the substitution is leucine substituted for phenylalanine 2200 corresponding to SEQ ID NO:2.

5. The modified human factor VIII of claim 1 wherein one of the substitution is phenylalanine substituted for leucine 2252 corresponding to SEQ ID NO:2.

6. The modified human factor VIII of claim 1 wherein two of the substitutions are isoleucine substituted for methionine 2199 and leucine substituted for phenylalanine 2200 corresponding to SEQ ID NO:2.

7. The modified human factor VIII of claim 1 wherein two of the substitutions are alanine substituted for valine 2223 and glutamate substituted for lysine 2227 corresponding to SEQ ID NO:2.

8. The modified human factor VIII of claim 1 wherein four of the substitutions are isoleucine substituted for methionine 2199, leucine substituted for phenylalanine 2200, alanine substituted for valine 2223, and glutamate substituted for lysine 2227 corresponding to SEQ ID NO:2.

9. The modified factor of claim 1 which has reduced antigenicity as compared to the corresponding human factor VIII protein.

10. The modified factor of claim 1 which has reduced immunogenicity as compared to the corresponding human factor VIII protein.

11. The modified factor VIII of claim 1 which has reduced immunogenicity and reduced antigenicity as compared to the corresponding human factor VIII protein.

12. The modified factor VIII of claim 1 which has a specific activity greater than about 2,000 units per milligram.

13. The modified factor VIII of claim 1 which has a specific activity greater than about 3,000 units per milligram.

14. The modified factor VIII of claim 1 which has a specific activity greater than about 5,000 units per milligram.

15. The modified factor VIII of claim 1 which has a specific activity greater than about 10,000 units per milligram.

16. The modified factor VIII of claim 1 which is a single mutant.

17. The modified factor VIII of claim 1 which is a double mutant.

18. The modified factor VIII of claim 1 which is a triple mutant.

19. The modified factor VIII of claim 1 which is a quadruple mutant.

20. The modified factor VIII of claim 1 which has lower antigenicity towards at least one C2-specific inhibitory antibody as compared to the corresponding human factor VIII from which the modified factor VIII was derived or full length recombinant factor VIII comprising the amino acid sequence of the corresponding human factor VIII.

21. The modified factor VIII of claim 1 which has an increased or decreased Bethesda titer of monoclonal antibody B02011 as compared to the corresponding human factor VIII from which the modified factor VIII was derived or full length recombinant factor VIII comprising the amino acid sequence of the corresponding human factor VIII.

22. The modified factor VIII of claim 1 which has an increased or decreased Bethesda titer of monoclonal antibody NMC VIII-5 as compared to the corresponding human factor VIII from which the modified factor VIII was derived or full length recombinant factor VIII comprising the amino acid sequence of the corresponding human factor VIII.

23. The modified factor VIII of claim 1 which has an increased or decreased Bethesda titer towards at least one inhibitory antibody preparation as compared to the corresponding human factor VIII from which the modified factor VIII was derived or full length recombinant factor VIII comprising the amino acid sequence of the corresponding human factor VIII.

24. A method for modifying human factor VIII such that reactivity to an inhibitory antibody is reduced and procoagulant activity is retained comprising substituting an amino acid in the C2 domain wherein the substitution is limited to at least one of the amino acids selected from the group consisting of 2199, 2200, 2223, 2227, 2251, and 2252 corresponding to SEQ ID NO:2.

25. The method of claim 24 wherein at least one of the substitutions is at position 2199 corresponding to SEQ ID NO:2.

26. The method of claim 24 wherein at least one of the substitutions is at position 2200 corresponding to SEQ ID NO:2.

27. The method of claim 24 wherein at least one of the substitutions is at position 2223 corresponding to SEQ ID NO:2.

28. The method of claim 24 wherein at least one of the substitutions is position 2227 corresponding to SEQ ID NO:2.

29. The method of claim 24 wherein at least one of the substitutions is position 2252 corresponding to SEQ ID NO:2.

30. The method of claim 24 wherein the modified factor VIII is a single mutant.

31. The method of claim 24 wherein the modified factor VIII is a double mutant.

32. The method of claim 24 wherein the modified factor VIII is a triple mutant.

33. The method of claim 24 wherein the modified factor VIII is a quadruple mutant.

34. A method for modifying human factor VIII such that antigenicity is reduced and procoagulant activity is retained comprising substituting an amino acid in the C2 domain wherein the substitution is limited to at least one of the amino acids at selected from the group consisting of 2199, 2200, 2223, 2227, 2251, and 2252 corresponding to SEQ ID NO:2.

35. The method of claim 34 wherein at least one of the substitutions is at position 2199 corresponding to SEQ ID NO:2.

36. The method of claim 34 wherein at least one of the substitutions is at position 2200 corresponding to SEQ ID NO:2.

37. The method of claim 34 wherein at least one of the substitutions is at position 2223 corresponding to SEQ ID NO:2.

38. The method of claim 34 wherein at least one of the substitutions is at position 2227 corresponding to SEQ ID NO:2.

39. The method of claim 34 wherein at least one of the substitutions is at position 2252 corresponding to SEQ ID NO:2.

40. The method of claim 34 wherein the modified factor VIII is a single mutant.

41. The method of claim 34 wherein the modified factor VIII is a double mutant.

42. The method of claim 34 wherein the modified factor VIII is a triple mutant.

43. The method of claim 34 wherein the modified factor VIII is a quadruple mutant.