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Volumn 112, Issue 5, 2014, Pages 972-980

Coagulation factor VII variants resistant to inhibitory antibodies

Author keywords

Carboxyl terminus; Factor VII deficiency; Inhibitory antibodies; Recombinant proteins; Replacement therapy

Indexed keywords

ANTIBODY; BLOOD CLOTTING FACTOR 10A; BLOOD CLOTTING FACTOR 7; IMMUNOGLOBULIN CLASS; IMMUNOGLOBULIN G1; IMMUNOGLOBULIN G2; IMMUNOGLOBULIN G3; IMMUNOGLOBULIN G4; INHIBITORY ANTIBODY; RECOMBINANT BLOOD CLOTTING FACTOR 7A; THROMBIN; UNCLASSIFIED DRUG; ALLOANTIBODY; BLOOD CLOTTING FACTOR 7A; IMMUNOGLOBULIN G; RECOMBINANT FVIIA; RECOMBINANT PROTEIN;

EID: 84908541961     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH14-03-0198     Document Type: Article
Times cited : (20)

References (41)
  • 1
    • 0029597912 scopus 로고
    • Factor VIII inhibitors in patients with haemophilia A: Epidemiology of inhibitor development and induction of immune tolerance for factor VIII
    • Kreuz W, Becker S, Lenz E, et al. Factor VIII inhibitors in patients with haemophilia A: epidemiology of inhibitor development and induction of immune tolerance for factor VIII. Semin Thromb Haemost 1995; 21: 382-389.
    • (1995) Semin Thromb Haemost , vol.21 , pp. 382-389
    • Kreuz, W.1    Becker, S.2    Lenz, E.3
  • 2
    • 34447128837 scopus 로고    scopus 로고
    • Inhibitor development in haemophilia B: An orphan disease in need of attention
    • DiMichele D. Inhibitor development in haemophilia B: an orphan disease in need of attention. Br J Haematol 2007; 138: 305-315.
    • (2007) Br J Haematol , vol.138 , pp. 305-315
    • DiMichele, D.1
  • 4
    • 84863419863 scopus 로고    scopus 로고
    • F8 gene mutation type and inhibitor development in patients with severe haemophilia A: Systematic review and meta-analysis
    • Gouw SC, van den Berg HM, Oldenburg J, et al. F8 gene mutation type and inhibitor development in patients with severe haemophilia A: systematic review and meta-analysis. Blood 2012; 119: 2922-2934.
    • (2012) Blood , vol.119 , pp. 2922-2934
    • Gouw, S.C.1    van den Berg, H.M.2    Oldenburg, J.3
  • 5
    • 34250708408 scopus 로고    scopus 로고
    • Treatment characteristics and the risk of inhibitor development: A multicenter cohort study among previously untreated patients with severe haemophilia A
    • Gouw SC, van den Berg HM, le Cessie S, et al. Treatment characteristics and the risk of inhibitor development: a multicenter cohort study among previously untreated patients with severe haemophilia A. J Thromb Haemost 2007; 5: 1383-1390.
    • (2007) J Thromb Haemost , vol.5 , pp. 1383-1390
    • Gouw, S.C.1    van den Berg, H.M.2    le Cessie, S.3
  • 7
    • 34548596676 scopus 로고    scopus 로고
    • Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: Report of a novel mutation (S103G)
    • Pruthi RK, Rodriguez V, Allen C, et al. Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: report of a novel mutation (S103G). Eur J Haematol 2007; 79: 354-359.
    • (2007) Eur J Haematol , vol.79 , pp. 354-359
    • Pruthi, R.K.1    Rodriguez, V.2    Allen, C.3
  • 8
    • 84355162163 scopus 로고    scopus 로고
    • Successful prophylactic use of recombinant activated factor VII (rFVIIa) in a patient with congenital FVII deficiency and inhibitors to FVII
    • Tokgoz H, Caliskan U, Lavigne-Lissalde G, et al. Successful prophylactic use of recombinant activated factor VII (rFVIIa) in a patient with congenital FVII deficiency and inhibitors to FVII. Haemophilia 2012; 18: e25-27.
    • (2012) Haemophilia , vol.18 , pp. e25-e27
    • Tokgoz, H.1    Caliskan, U.2    Lavigne-Lissalde, G.3
  • 9
    • 84894091165 scopus 로고    scopus 로고
    • Inhibitors to factor VII and in congenital factor VII deficiency
    • Batorova A, Mariani G, Kavakli K, et al., on behalf of the STER Study Group. Inhibitors to factor VII and in congenital factor VII deficiency. Haemophilia 2014; 20: e188-191.
    • (2014) Haemophilia , vol.20 , pp. e188-e191
    • Batorova, A.1    Mariani, G.2    Kavakli, K.3
  • 10
    • 0025287330 scopus 로고
    • Comparative modeling methods: Application to the family of the mammalian serine proteases
    • Greer J. Comparative modeling methods: application to the family of the mammalian serine proteases. Proteins 1990; 7: 317-334.
    • (1990) Proteins , vol.7 , pp. 317-334
    • Greer, J.1
  • 11
    • 0027123107 scopus 로고
    • Molecular and cellular biology of blood coagulation
    • Furie B, Furie BC. Molecular and cellular biology of blood coagulation. N Engl J Med 1992; 326: 800-806.
    • (1992) N Engl J Med , vol.326 , pp. 800-806
    • Furie, B.1    Furie, B.C.2
  • 12
    • 20144382370 scopus 로고    scopus 로고
    • Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
    • Mariani G, Herrmann FH, Dolce A, et al., International Factor VIIDSG. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 2005; 93: 481-487.
    • (2005) Thromb Haemost , vol.93 , pp. 481-487
    • Mariani, G.1    Herrmann, F.H.2    Dolce, A.3    International Factor VIIDSG4
  • 13
    • 0030775316 scopus 로고    scopus 로고
    • Mice lacking factor VII develop normally but suffer fatal perinatal bleeding
    • Rosen ED, Chan JC, Idusogie E, et al. Mice lacking factor VII develop normally but suffer fatal perinatal bleeding. Nature 1997; 390: 290-294.
    • (1997) Nature , vol.390 , pp. 290-294
    • Rosen, E.D.1    Chan, J.C.2    Idusogie, E.3
  • 14
    • 0031057651 scopus 로고    scopus 로고
    • HLA class II profile: A weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party
    • Hay CR, Ollier W, Pepper L, et al. HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party. Thromb Haemost 1997; 77: 234-237.
    • (1997) Thromb Haemost , vol.77 , pp. 234-237
    • Hay, C.R.1    Ollier, W.2    Pepper, L.3
  • 15
    • 33751014075 scopus 로고    scopus 로고
    • Genetic risk factors for inhibitors to factors VIII and IX
    • Oldenburg J, Pavlova A. Genetic risk factors for inhibitors to factors VIII and IX. Haemophilia 2006; 12 (Suppl 6): 15-22.
    • (2006) Haemophilia , vol.12 , pp. 15-22
    • Oldenburg, J.1    Pavlova, A.2
  • 16
    • 84874393543 scopus 로고    scopus 로고
    • The polygenic nature of inhibitors in haemophilia A: Results from the Haemophilia Inhibitor Genetics Study (HIGS) Combined Cohort
    • Astermark J, Donfield SM, Gomperts ED, et al., Haemophilia Inhibitor Genetics Study Combined C. The polygenic nature of inhibitors in haemophilia A: results from the Haemophilia Inhibitor Genetics Study (HIGS) Combined Cohort. Blood 2013; 121: 1446-1454.
    • (2013) Blood , vol.121 , pp. 1446-1454
    • Astermark, J.1    Donfield, S.M.2    Gomperts, E.D.3    Haemophilia Inhibitor Genetics Study Combined C4
  • 17
    • 77449101167 scopus 로고    scopus 로고
    • Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-alpha and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe haemophilia A
    • Pavlova A, Delev D, Lacroix-Desmazes S, et al. Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-alpha and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe haemophilia A. J Thromb Haemost 2009; 7: 2006-2015.
    • (2009) J Thromb Haemost , vol.7 , pp. 2006-2015
    • Pavlova, A.1    Delev, D.2    Lacroix-Desmazes, S.3
  • 18
    • 0036164276 scopus 로고    scopus 로고
    • Haemophilia A and haemophilia B: Molecular insights
    • Bowen DJ. Haemophilia A and haemophilia B: molecular insights. Mol Pathol 2002; 55: 1-18.
    • (2002) Mol Pathol , vol.55 , pp. 1-18
    • Bowen, D.J.1
  • 19
    • 84874766491 scopus 로고    scopus 로고
    • Significance of F8 missense mutations with respect to inhibitor formation
    • Schwaab R, Pavlova A, Albert T, et al. Significance of F8 missense mutations with respect to inhibitor formation. Thromb Haemost 2013; 109: 464-470.
    • (2013) Thromb Haemost , vol.109 , pp. 464-470
    • Schwaab, R.1    Pavlova, A.2    Albert, T.3
  • 20
    • 0842333021 scopus 로고    scopus 로고
    • Intensive exposure to factor VIII is a risk factor for inhibitor development in mild haemophilia A
    • Sharathkumar A, Lillicrap D, Blanchette VS, et al. Intensive exposure to factor VIII is a risk factor for inhibitor development in mild haemophilia A. J Thromb Haemost 2003; 1: 1228-1236.
    • (2003) J Thromb Haemost , vol.1 , pp. 1228-1236
    • Sharathkumar, A.1    Lillicrap, D.2    Blanchette, V.S.3
  • 21
    • 0028059812 scopus 로고
    • Molecular analysis of Polish patients with factor VII deficiency
    • Arbini AA, Bodkin D, Lopaciuk S, et al. Molecular analysis of Polish patients with factor VII deficiency. Blood 1994; 84: 2214-2220.
    • (1994) Blood , vol.84 , pp. 2214-2220
    • Arbini, A.A.1    Bodkin, D.2    Lopaciuk, S.3
  • 22
    • 0034091518 scopus 로고    scopus 로고
    • Twenty two novel mutations of the factor VII gene in factor VII deficiency
    • Wulff K, Herrmann FH. Twenty two novel mutations of the factor VII gene in factor VII deficiency. Hum Mutat 2000; 15: 489-496.
    • (2000) Hum Mutat , vol.15 , pp. 489-496
    • Wulff, K.1    Herrmann, F.H.2
  • 23
    • 18344405441 scopus 로고    scopus 로고
    • A detailed comparison of the performance of the standard versus the Nijmegen modification of the Bethesda assay in detecting factor VIII: C inhibitors in the haemophilia A population of Canada. Association of Haemophilia Centre Directors of Canada. Factor VIII/IX Subcommittee of Scientific and Standardisation Committee of International Society on Thrombosis and Haemostasis
    • Giles AR, Verbruggen B, Rivard GE, et al. A detailed comparison of the performance of the standard versus the Nijmegen modification of the Bethesda assay in detecting factor VIII: C inhibitors in the haemophilia A population of Canada. Association of Haemophilia Centre Directors of Canada. Factor VIII/IX Subcommittee of Scientific and Standardisation Committee of International Society on Thrombosis and Haemostasis. Thromb Haemost 1998; 79: 872-875.
    • (1998) Thromb Haemost , vol.79 , pp. 872-875
    • Giles, A.R.1    Verbruggen, B.2    Rivard, G.E.3
  • 24
    • 84860587422 scopus 로고    scopus 로고
    • Natural and engineered carboxy-terminal variants: Decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency
    • Branchini A, Rizzotto L, Mariani G, et al. Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency. Haematologica 2012; 97: 705-709.
    • (2012) Haematologica , vol.97 , pp. 705-709
    • Branchini, A.1    Rizzotto, L.2    Mariani, G.3
  • 25
    • 33644855157 scopus 로고    scopus 로고
    • Molecular bases of type II protein S deficiency: The I203-D204 deletion in the EGF4 domain alters GLA domain function
    • Baroni M, Mazzola G, Kaabache T, et al. Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function. J Thromb Haemost 2006; 4: 186-191.
    • (2006) J Thromb Haemost , vol.4 , pp. 186-191
    • Baroni, M.1    Mazzola, G.2    Kaabache, T.3
  • 26
    • 70349264566 scopus 로고    scopus 로고
    • Characteristics, mechanisms of action, and epitope mapping of anti-factor VIII antibodies
    • Lavigne-Lissalde G, Rothschild C, Pouplard C, et al. Characteristics, mechanisms of action, and epitope mapping of anti-factor VIII antibodies. Clin Rev Allergy Immunol 2009; 37: 67-79.
    • (2009) Clin Rev Allergy Immunol , vol.37 , pp. 67-79
    • Lavigne-Lissalde, G.1    Rothschild, C.2    Pouplard, C.3
  • 27
    • 84861673289 scopus 로고    scopus 로고
    • Validation of Nijmegen-Bethesda assay modifications to allow inhibitor measure-ment during replacement therapy and facilitate inhibitor surveillance
    • Miller CH, Platt SJ, Rice AS, et al., Haemophilia Inhibitor Research Study I. Validation of Nijmegen-Bethesda assay modifications to allow inhibitor measure-ment during replacement therapy and facilitate inhibitor surveillance. J Thromb Haemost 2012; 10: 1055-1061.
    • (2012) J Thromb Haemost , vol.10 , pp. 1055-1061
    • Miller, C.H.1    Platt, S.J.2    Rice, A.S.3    Haemophilia Inhibitor Research Study I4
  • 28
    • 0036797888 scopus 로고    scopus 로고
    • The thrombogram in rare inherited coagulation disorders: Its relation to clinical bleeding
    • Al Dieri R, Peyvandi F, Santagostino E, et al. The thrombogram in rare inherited coagulation disorders: its relation to clinical bleeding. Thromb Haemost 2002; 88: 576-582.
    • (2002) Thromb Haemost , vol.88 , pp. 576-582
    • Al Dieri, R.1    Peyvandi, F.2    Santagostino, E.3
  • 29
    • 79251495773 scopus 로고    scopus 로고
    • Thrombin generation tests
    • Castoldi E, Rosing J. Thrombin generation tests. Thromb Res 2011; 127 (Suppl 3): S21-25.
    • (2011) Thromb Res , vol.127 , pp. S21-S25
    • Castoldi, E.1    Rosing, J.2
  • 30
    • 84902300521 scopus 로고    scopus 로고
    • Factor II activity is similarly increased in patients with elevated apolipoprotein CIII and in carriers of the factor II 20210A allele
    • Olivieri O, Martinelli N, Baroni M, et al. Factor II activity is similarly increased in patients with elevated apolipoprotein CIII and in carriers of the factor II 20210A allele. J Am Heart Assoc 2013; 2: e000440.
    • (2013) J Am Heart Assoc , vol.2
    • Olivieri, O.1    Martinelli, N.2    Baroni, M.3
  • 31
    • 33751008103 scopus 로고    scopus 로고
    • Immunological aspects of inhibitor development
    • Reding MT. Immunological aspects of inhibitor development. Haemophilia 2006; 12 Suppl 6: 30-36.
    • (2006) Haemophilia , vol.12 , pp. 30-36
    • Reding, M.T.1
  • 32
    • 47649116958 scopus 로고    scopus 로고
    • IgG subclasses of anti-FVIII antibodies during immune tolerance induction in patients with haemophilia A
    • van Helden PM, van den Berg HM, Gouw SC, et al. IgG subclasses of anti-FVIII antibodies during immune tolerance induction in patients with haemophilia A. Br Journal Haematol 2008; 142: 644-652.
    • (2008) Br Journal Haematol , vol.142 , pp. 644-652
    • van Helden, P.M.1    van den Berg, H.M.2    Gouw, S.C.3
  • 33
    • 0034941729 scopus 로고    scopus 로고
    • The factor VII zymogen structure reveals reregistration of beta strands during activation
    • Eigenbrot C, Kirchhofer D, Dennis MS, et al. The factor VII zymogen structure reveals reregistration of beta strands during activation. Structure. 2001; 9: 627-636.
    • (2001) Structure , vol.9 , pp. 627-636
    • Eigenbrot, C.1    Kirchhofer, D.2    Dennis, M.S.3
  • 34
    • 34547402616 scopus 로고    scopus 로고
    • Engineering the substrate and inhibitor specificities of human coagulation Factor VIIa
    • Larsen KS, Østergaard H, Bjelke JR, et al. Engineering the substrate and inhibitor specificities of human coagulation Factor VIIa. Biochem J 2007; 405: 429-438.
    • (2007) Biochem J , vol.405 , pp. 429-438
    • Larsen, K.S.1    Østergaard, H.2    Bjelke, J.R.3
  • 35
    • 82355161117 scopus 로고    scopus 로고
    • Recombinant factor VIIa analog NN1731 (V158D/E296V/M298Q-FVIIa) enhances fibrin formation, structure and stability in lipidated haemophilic plasma
    • Gray LD, Hussey MA, Larson BM, et al. Recombinant factor VIIa analog NN1731 (V158D/E296V/M298Q-FVIIa) enhances fibrin formation, structure and stability in lipidated haemophilic plasma. Thromb Res 2011; 128: 570-576.
    • (2011) Thromb Res , vol.128 , pp. 570-576
    • Gray, L.D.1    Hussey, M.A.2    Larson, B.M.3
  • 36
    • 43749102313 scopus 로고    scopus 로고
    • Prolonged in-vivo half-life of factor VIIa by fusion to albumin
    • Weimer T, Wormsbacher W, Kronthaler U, et al. Prolonged in-vivo half-life of factor VIIa by fusion to albumin. Thromb Haemost 2008; 99: 659-667.
    • (2008) Thromb Haemost , vol.99 , pp. 659-667
    • Weimer, T.1    Wormsbacher, W.2    Kronthaler, U.3
  • 37
    • 77952542376 scopus 로고    scopus 로고
    • Recombinant coagulation factor VIIa-from molecular to clinical aspects of a versatile haemostatic agent
    • Persson E, Bolt G, Steenstrup TD, et al. Recombinant coagulation factor VIIa-from molecular to clinical aspects of a versatile haemostatic agent. Thromb Res 2010; 125: 483-489.
    • (2010) Thromb Res , vol.125 , pp. 483-489
    • Persson, E.1    Bolt, G.2    Steenstrup, T.D.3
  • 38
    • 34247876261 scopus 로고    scopus 로고
    • Treatment of acquired haemophilia A
    • Collins PW. Treatment of acquired haemophilia A. J Thromb Haemost 2007; 5: 893-900.
    • (2007) J Thromb Haemost , vol.5 , pp. 893-900
    • Collins, P.W.1
  • 39
    • 4544229639 scopus 로고    scopus 로고
    • Recombinant factor VIIa: Review of efficacy, dosing regimens and safety in patients with congenital and acquired factor VIII or IX inhibitors
    • Abshire T, Kenet G. Recombinant factor VIIa: review of efficacy, dosing regimens and safety in patients with congenital and acquired factor VIII or IX inhibitors. J Thromb Haemost 2004; 2: 899-909.
    • (2004) J Thromb Haemost , vol.2 , pp. 899-909
    • Abshire, T.1    Kenet, G.2
  • 40
    • 79953294918 scopus 로고    scopus 로고
    • T-cell responses in two unrelated haemophilia A inhibitor subjects include an epitope at the factor VIII R593C missense site
    • James EA, van Haren SD, Ettinger RA, et al. T-cell responses in two unrelated haemophilia A inhibitor subjects include an epitope at the factor VIII R593C missense site. J Thromb Haemost 2011; 9: 689-699.
    • (2011) J Thromb Haemost , vol.9 , pp. 689-699
    • James, E.A.1    van Haren, S.D.2    Ettinger, R.A.3
  • 41
    • 65849180700 scopus 로고    scopus 로고
    • Intensive peri-operative use of factor VIII and the Arg593->Cys mutation are risk factors for inhibitor development in mild/moderate haemophilia A
    • Eckhardt CL, Menke LA, van Ommen CH, et al. Intensive peri-operative use of factor VIII and the Arg593->Cys mutation are risk factors for inhibitor development in mild/moderate haemophilia A. J Thromb Haemost 2009; 7: 930-937.
    • (2009) J Thromb Haemost , vol.7 , pp. 930-937
    • Eckhardt, C.L.1    Menke, L.A.2    van Ommen, C.H.3


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