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Volumn 35, Issue 8, 2009, Pages 723-734

The multifactorial etiology of inhibitor development in hemophilia: Genetics and environment

Author keywords

Factor VIII inhibitors; Factor VIII mutation; Genetic polymorphisms; Intensive treatment; Prophylaxis; Risk factors

Indexed keywords

BLOOD CLOTTING FACTOR 8; TRANSFORMING GROWTH FACTOR BETA;

EID: 77449116760     PISSN: 00946176     EISSN: 10989064     Source Type: Journal    
DOI: 10.1055/s-0029-1245105     Document Type: Review
Times cited : (96)

References (102)
  • 1
    • 0035077234 scopus 로고    scopus 로고
    • Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis
    • Factor VIII and Factor IX Subcommittee
    • White G C. II, Rosendaal F, Aledort L M., Lusher J M., Rothschild C, Ingerslev J, Factor VIII and Factor IX Subcommittee. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 2001 85 (3) 560
    • (2001) Thromb Haemost , vol.85 , Issue.3 , pp. 560
    • White Ii, G.C.1    Rosendaal, F.2    Aledort, L.M.3    Lusher, J.M.4    Rothschild, C.5    Ingerslev, J.6
  • 2
    • 41349105729 scopus 로고    scopus 로고
    • Social participation of patients with hemophilia in the Netherlands
    • Plug I, Peters M, Mauser-Bunschoten E P. et al. Social participation of patients with hemophilia in the Netherlands. Blood 2008 111 (4) 1811-1815
    • (2008) Blood , vol.111 , Issue.4 , pp. 1811-1815
    • Plug, I.1    Peters, M.2    Mauser-Bunschoten, E.P.3
  • 3
    • 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 (3) 305-315
    • (2007) Br J Haematol , vol.138 , Issue.3 , pp. 305-315
    • Dimichele, D.1
  • 4
    • 0038383605 scopus 로고    scopus 로고
    • The epidemiology of inhibitors in haemophilia A: A systematic review
    • Wight J, Paisley S. The epidemiology of inhibitors in haemophilia A: a systematic review. Haemophilia 2003 9 (4) 418-435
    • (2003) Haemophilia , vol.9 , Issue.4 , pp. 418-435
    • Wight, J.1    Paisley, S.2
  • 5
    • 33751017721 scopus 로고    scopus 로고
    • Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates
    • Kempton C L., Soucie J M., Abshire T C. Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates. J Thromb Haemost 2006 4 (12) 2576-2581
    • (2006) J Thromb Haemost , vol.4 , Issue.12 , pp. 2576-2581
    • Kempton, C.L.1    Soucie, J.M.2    Abshire, T.C.3
  • 6
    • 9144271883 scopus 로고    scopus 로고
    • The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 197799
    • UK Haemophilia Centre Doctors' Organisation
    • Darby S C., Keeling D M., Spooner R J. et al, UK Haemophilia Centre Doctors' Organisation. The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 197799. J Thromb Haemost 2004 2 (7) 1047-1054
    • (2004) J Thromb Haemost , vol.2 , Issue.7 , pp. 1047-1054
    • Darby, S.C.1    Keeling, D.M.2    Spooner, R.J.3
  • 7
    • 34548304886 scopus 로고    scopus 로고
    • European study on orthopaedic status of haemophilia patients with inhibitors
    • Morfini M, Haya S, Tagariello G et al. European study on orthopaedic status of haemophilia patients with inhibitors. Haemophilia 2007 13 (5) 606-612
    • (2007) Haemophilia , vol.13 , Issue.5 , pp. 606-612
    • Morfini, M.1    Haya, S.2    Tagariello, G.3
  • 8
    • 0141482007 scopus 로고    scopus 로고
    • Cost of care and quality of life for patients with hemophilia complicated by inhibitors: The COCIS Study Group
    • COCIS Study Group
    • Gringeri A, Mantovani L G., Scalone L, Mannucci P M., COCIS Study Group. Cost of care and quality of life for patients with hemophilia complicated by inhibitors: the COCIS Study Group. Blood 2003 102 (7) 2358-2363
    • (2003) Blood , vol.102 , Issue.7 , pp. 2358-2363
    • Gringeri, A.1    Mantovani, L.G.2    Scalone, L.3    Mannucci, P.M.4
  • 9
    • 0038383604 scopus 로고    scopus 로고
    • Immune tolerance induction in patients with haemophilia A with inhibitors: A systematic review
    • Wight J, Paisley S, Knight C. Immune tolerance induction in patients with haemophilia A with inhibitors: a systematic review. Haemophilia 2003 9 (4) 436-463 (Pubitemid 36874392)
    • (2003) Haemophilia , vol.9 , Issue.4 , pp. 436-463
    • Wight, J.1    Paisley, S.2    Knight, C.3
  • 10
    • 36348975208 scopus 로고    scopus 로고
    • Delays in maturation among adolescents with hemophilia and a history of inhibitors
    • for the Hemophilia Growth and Development Study Group
    • Donfield S M., Lynn H S., Lail A E., Hoots W K., Berntorp E, Gomperts E D., for the Hemophilia Growth and Development Study Group. Delays in maturation among adolescents with hemophilia and a history of inhibitors. Blood 2007 110 (10) 3656-3661
    • (2007) Blood , vol.110 , Issue.10 , pp. 3656-3661
    • Donfield, S.M.1    Lynn, H.S.2    Lail, A.E.3    Hoots, W.K.4    Berntorp, E.5    Gomperts, E.D.6
  • 11
    • 76149093682 scopus 로고    scopus 로고
    • Laboratory identification of factor inhibitors: The perspective of a large tertiary hemophilia centre
    • Kershaw G, Jayakodi D, Dunkley S. Laboratory identification of factor inhibitors: the perspective of a large tertiary hemophilia centre. Semin Thromb Hemost 2009 35 (8) 760-768
    • (2009) Semin Thromb Hemost , vol.35 , Issue.8 , pp. 760-768
    • Kershaw, G.1    Jayakodi, D.2    Dunkley, S.3
  • 12
    • 0028837315 scopus 로고
    • The Nijmegen modification of the Bethesda assay for factor VIII:C inhibitors: Improved specificity and reliability
    • Verbruggen B, Novakova I, Wessels H, Boezeman J, van den Berg M, Mauser-Bunschoten E. The Nijmegen modification of the Bethesda assay for factor VIII:C inhibitors: improved specificity and reliability. Thromb Haemost 1995 73 (2) 247-251
    • (1995) Thromb Haemost , vol.73 , Issue.2 , pp. 247-251
    • Verbruggen, B.1    Novakova, I.2    Wessels, H.3    Boezeman, J.4    Van Den Berg, M.5    Mauser-Bunschoten, E.6
  • 13
    • 65349196134 scopus 로고    scopus 로고
    • Laboratory assessment of factor VIII inhibitor titer: The North American Specialized Coagulation Laboratory Association experience
    • NASCOLA Proficiency Testing Committee
    • Peerschke E I., Castellone D D., Ledford-Kraemer M, Van Cott E M., Meijer P, NASCOLA Proficiency Testing Committee. Laboratory assessment of factor VIII inhibitor titer: the North American Specialized Coagulation Laboratory Association experience. Am J Clin Pathol 2009 131 (4) 552-558
    • (2009) Am J Clin Pathol , vol.131 , Issue.4 , pp. 552-558
    • Peerschke, E.I.1    Castellone, D.D.2    Ledford-Kraemer, M.3    Van Cott, E.M.4    Meijer, P.5
  • 14
    • 0029617930 scopus 로고
    • Haemophilia A: Mutation type determines risk of inhibitor formation
    • Schwaab R, Brackmann H H., Meyer C et al. Haemophilia A: mutation type determines risk of inhibitor formation. Thromb Haemost 1995 74 (6) 1402-1406
    • (1995) Thromb Haemost , vol.74 , Issue.6 , pp. 1402-1406
    • Schwaab, R.1    Brackmann, H.H.2    Meyer, C.3
  • 15
    • 0034124571 scopus 로고    scopus 로고
    • Relationship between factor VIII mutation type and inhibitor development in a cohort of previously untreated patients treated with recombinant factor VIII (Recombinate)
    • Recombinate PUP Study Group
    • Goodeve A C., Williams I, Bray G L., Peake I R., Recombinate PUP Study Group. Relationship between factor VIII mutation type and inhibitor development in a cohort of previously untreated patients treated with recombinant factor VIII (Recombinate). Thromb Haemost 2000 83 (6) 844-848
    • (2000) Thromb Haemost , vol.83 , Issue.6 , pp. 844-848
    • Goodeve, A.C.1    Williams, I.2    Bray, G.L.3    Peake, I.R.4
  • 16
    • 22544473061 scopus 로고    scopus 로고
    • The Malm International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A
    • Malm International Brother Study group
    • Astermark J, Oldenburg J, Escobar M, White G C. II, Berntorp E, Malm International Brother Study group. The Malm International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A. Haematologica 2005 90 (7) 924-931
    • (2005) Haematologica , vol.90 , Issue.7 , pp. 924-931
    • Astermark, J.1    Oldenburg, J.2    Escobar, M.3    White Ii, G.C.4    Berntorp, E.5
  • 17
    • 33645730547 scopus 로고    scopus 로고
    • Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France. Description of 62 novel mutations
    • Vinciguerra C, Zawadzki C, Dargaud Y et al. Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France. Description of 62 novel mutations. Thromb Haemost 2006 95 (4) 593-599
    • (2006) Thromb Haemost , vol.95 , Issue.4 , pp. 593-599
    • Vinciguerra, C.1    Zawadzki, C.2    Dargaud, Y.3
  • 18
    • 0031856834 scopus 로고    scopus 로고
    • The genetic basis of inhibitor development in haemophilia A
    • Tuddenham E G., McVey J H. The genetic basis of inhibitor development in haemophilia A. Haemophilia 1998 4 (4) 543-545
    • (1998) Haemophilia , vol.4 , Issue.4 , pp. 543-545
    • Tuddenham, E.G.1    McVey, J.H.2
  • 19
    • 0033710529 scopus 로고    scopus 로고
    • Risk factors for inhibitor development in hemophilia A
    • discussion 13-14
    • Oldenburg J, Brackmann H H., Schwaab R. Risk factors for inhibitor development in hemophilia A. Haematologica 2000 85 (Suppl 10) 7-13 discussion 13-14
    • (2000) Haematologica , vol.85 , Issue.SUPPL 10 , pp. 7-13
    • Oldenburg, J.1    Brackmann, H.H.2    Schwaab, R.3
  • 20
    • 0037330233 scopus 로고    scopus 로고
    • The molecular basis of hemophilia A: Genotype-phenotype relationships and inhibitor development
    • Goodeve A C., Peake I R. The molecular basis of hemophilia A: genotype-phenotype relationships and inhibitor development. Semin Thromb Hemost 2003 29 (1) 23-30
    • (2003) Semin Thromb Hemost , vol.29 , Issue.1 , pp. 23-30
    • Goodeve, A.C.1    Peake, I.R.2
  • 21
    • 0031989414 scopus 로고    scopus 로고
    • Small deletion/insertion mutations within poly-A runs of the factor VIII gene mitigate the severe haemophilia A phenotype
    • Oldenburg J, Schrder J, Schmitt C, Brackmann H H., Schwaab R. Small deletion/insertion mutations within poly-A runs of the factor VIII gene mitigate the severe haemophilia A phenotype. Thromb Haemost 1998 79 (2) 452-453
    • (1998) Thromb Haemost , vol.79 , Issue.2 , pp. 452-453
    • Oldenburg, J.1    Schrder, J.2    Schmitt, C.3    Brackmann, H.H.4    Schwaab, R.5
  • 22
    • 0017653247 scopus 로고
    • Genetic predisposition to develop factor VIII antibody in classic hemophilia
    • Frommel D, Allain J P. Genetic predisposition to develop factor VIII antibody in classic hemophilia. Clin Immunol Immunopathol 1977 8 (1) 34-38
    • (1977) Clin Immunol Immunopathol , vol.8 , Issue.1 , pp. 34-38
    • Frommel, D.1    Allain, J.P.2
  • 23
    • 0021314059 scopus 로고
    • Genetic predisposition to inhibitor formation
    • Shapiro S S. Genetic predisposition to inhibitor formation. Prog Clin Biol Res 1984 150 45-55
    • (1984) Prog Clin Biol Res , vol.150 , pp. 45-55
    • Shapiro, S.S.1
  • 24
    • 6644227418 scopus 로고    scopus 로고
    • The Malm International Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients
    • MIBS Study Group
    • Astermark J, Berntorp E, White G C., Kroner B L., MIBS Study Group. The Malm International Brother Study (MIBS): further support for genetic predisposition to inhibitor development in hemophilia patients. Haemophilia 2001 7 (3) 267-272
    • (2001) Haemophilia , vol.7 , Issue.3 , pp. 267-272
    • Astermark, J.1    Berntorp, E.2    White, G.C.3    Kroner, B.L.4
  • 25
    • 0031598278 scopus 로고    scopus 로고
    • Inhibitors occur more frequently in African-American and Latino haemophiliacs
    • Aledort L M., Dimichele D M. Inhibitors occur more frequently in African-American and Latino haemophiliacs. Haemophilia 1998 4 (1) 68
    • (1998) Haemophilia , vol.4 , Issue.1 , pp. 68
    • Aledort, L.M.1    Dimichele, D.M.2
  • 26
    • 0032787813 scopus 로고    scopus 로고
    • Incidence of inhibitors in haemophilia A patientsa review of recent studies of recombinant and plasma-derived factor VIII concentrates
    • Scharrer I, Bray G L., Neutzling O. Incidence of inhibitors in haemophilia A patientsa review of recent studies of recombinant and plasma-derived factor VIII concentrates. Haemophilia 1999 5 (3) 145-154
    • (1999) Haemophilia , vol.5 , Issue.3 , pp. 145-154
    • Scharrer, I.1    Bray, G.L.2    Neutzling, O.3
  • 27
    • 64749096663 scopus 로고    scopus 로고
    • Inhibitors of factor VIII in black patients with hemophilia
    • Viel K R., Ameri A, Abshire T C. et al. Inhibitors of factor VIII in black patients with hemophilia. N Engl J Med 2009 360 (16) 1618-1627
    • (2009) N Engl J Med , vol.360 , Issue.16 , pp. 1618-1627
    • Viel, K.R.1    Ameri, A.2    Abshire, T.C.3
  • 28
    • 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 C R., Ollier W, Pepper L et al, UKHCDO Inhibitor Working Party. HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. Thromb Haemost 1997 77 (2) 234-237
    • (1997) Thromb Haemost , vol.77 , Issue.2 , pp. 234-237
    • Hay, C.R.1    Ollier, W.2    Pepper, L.3
  • 29
    • 0031045680 scopus 로고    scopus 로고
    • HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII
    • Oldenburg J, Picard J K., Schwaab R, Brackmann H H., Tuddenham E G., Simpson E. HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII. Thromb Haemost 1997 77 (2) 238-242
    • (1997) Thromb Haemost , vol.77 , Issue.2 , pp. 238-242
    • Oldenburg, J.1    Picard, J.K.2    Schwaab, R.3    Brackmann, H.H.4    Tuddenham, E.G.5    Simpson, E.6
  • 30
    • 0019805248 scopus 로고
    • HLA antigens and factor VIII antibody in classic hemophilia. European study group of factor VIII antibody
    • Frommel D, Allain J P., Saint-Paul E et al. HLA antigens and factor VIII antibody in classic hemophilia. European study group of factor VIII antibody. Thromb Haemost 1981 46 (4) 687-689
    • (1981) Thromb Haemost , vol.46 , Issue.4 , pp. 687-689
    • Frommel, D.1    Allain, J.P.2    Saint-Paul, E.3
  • 32
    • 0025614887 scopus 로고
    • Relationship of major histocompatibility complex class II genes to inhibitor antibody formation in hemophilia A
    • Lippert L E., Fisher L M., Schook L B. Relationship of major histocompatibility complex class II genes to inhibitor antibody formation in hemophilia A. Thromb Haemost 1990 64 (4) 564-568
    • (1990) Thromb Haemost , vol.64 , Issue.4 , pp. 564-568
    • Lippert, L.E.1    Fisher, L.M.2    Schook, L.B.3
  • 33
    • 33845239946 scopus 로고    scopus 로고
    • Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A
    • Astermark J, Oldenburg J, Carlson J et al. Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A. Blood 2006 108 (12) 3739-3745
    • (2006) Blood , vol.108 , Issue.12 , pp. 3739-3745
    • Astermark, J.1    Oldenburg, J.2    Carlson, J.3
  • 34
    • 0021248705 scopus 로고
    • Markers for the factor VIII antibody response in hemophilia A
    • Shapiro S S. Markers for the factor VIII antibody response in hemophilia A. Scand J Haematol Suppl 1984 40 181-185
    • (1984) Scand J Haematol Suppl , vol.40 , pp. 181-185
    • Shapiro, S.S.1
  • 35
    • 0013585229 scopus 로고
    • Major histocompatibility complex (MHC)-linked complement alleles as markers for the development of anti-factor VIII in hemophiliacs
    • Alper C A., Raum D D., Awdeh Z L., Shapiro S S., Yunis E J. Major histocompatibility complex (MHC)-linked complement alleles as markers for the development of anti-factor VIII in hemophiliacs. Prog Clin Biol Res 1984 150 141-142
    • (1984) Prog Clin Biol Res , vol.150 , pp. 141-142
    • Alper, C.A.1    Raum, D.D.2    Awdeh, Z.L.3    Shapiro, S.S.4    Yunis, E.J.5
  • 36
    • 0021893526 scopus 로고
    • HLA antigens in hemophiliacs A with or without factor VIII antibodies in a Venezuelan mestizo population
    • Simonney N, De Bosch N, Argueyo A, Garcia E, Layrisse Z. HLA antigens in hemophiliacs A with or without factor VIII antibodies in a Venezuelan mestizo population. Tissue Antigens 1985 25 (4) 216-219
    • (1985) Tissue Antigens , vol.25 , Issue.4 , pp. 216-219
    • Simonney, N.1    De Bosch, N.2    Argueyo, A.3    Garcia, E.4    Layrisse, Z.5
  • 37
    • 0022445747 scopus 로고
    • High frequency of HLA-DR5 in Greek patients with haemophilia A and haemophilia B
    • Papasteriades C, Varla M, Economidou J et al. High frequency of HLA-DR5 in Greek patients with haemophilia A and haemophilia B. Tissue Antigens 1986 28 (2) 84-87
    • (1986) Tissue Antigens , vol.28 , Issue.2 , pp. 84-87
    • Papasteriades, C.1    Varla, M.2    Economidou, J.3
  • 38
    • 0025502132 scopus 로고
    • Histocompatibility antigen patterns in haemophilic patients with factor VIII antibodies
    • Aly A M., Aledort L M., Lee T D., Hoyer L W. Histocompatibility antigen patterns in haemophilic patients with factor VIII antibodies. Br J Haematol 1990 76 (2) 238-241
    • (1990) Br J Haematol , vol.76 , Issue.2 , pp. 238-241
    • Aly, A.M.1    Aledort, L.M.2    Lee, T.D.3    Hoyer, L.W.4
  • 39
    • 0032812613 scopus 로고    scopus 로고
    • Histocompatibility antigens and alleles in Japanese haemophilia A patients with or without factor VIII antibodies
    • Ohta H, Takahashi I, Kojima T et al. Histocompatibility antigens and alleles in Japanese haemophilia A patients with or without factor VIII antibodies. Tissue Antigens 1999 54 (1) 91-97
    • (1999) Tissue Antigens , vol.54 , Issue.1 , pp. 91-97
    • Ohta, H.1    Takahashi, I.2    Kojima, T.3
  • 40
    • 54549122596 scopus 로고    scopus 로고
    • Inhibitor-Immunology-Study. Different HLA-types seem to be involved in the inhibitor development in haemophilia A
    • Wieland I, Wermes C, Eifrig B et al. Inhibitor-Immunology-Study. Different HLA-types seem to be involved in the inhibitor development in haemophilia A. Hamostaseologie 2008 28 (suppl 1) S26-S28
    • (2008) Hamostaseologie , vol.28 , Issue.SUPPL 1
    • Wieland, I.1    Wermes, C.2    Eifrig, B.3
  • 41
    • 69949099131 scopus 로고    scopus 로고
    • Risk factors for inhibitor formation in haemophilia: A prevalent case-control study
    • Ragni M V., Ojeifo O, Feng J et al. Risk factors for inhibitor formation in haemophilia: a prevalent case-control study. Haemophilia 2009 15 (5) 1074-1082
    • (2009) Haemophilia , vol.15 , Issue.5 , pp. 1074-1082
    • Ragni, M.V.1    Ojeifo, O.2    Feng, J.3
  • 42
    • 33645751563 scopus 로고    scopus 로고
    • Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A
    • MIBS Study Group
    • Astermark J, Oldenburg J, Pavlova A, Berntorp E, Lefvert A K., MIBS Study Group. Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A. Blood 2006 107 (8) 3167-3172
    • (2006) Blood , vol.107 , Issue.8 , pp. 3167-3172
    • Astermark, J.1    Oldenburg, J.2    Pavlova, A.3    Berntorp, E.4    Lefvert, A.K.5
  • 43
    • 33846420672 scopus 로고    scopus 로고
    • Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A
    • MIBS Study Group
    • Astermark J, Wang X, Oldenburg J, Berntorp E, Lefvert A K., MIBS Study Group. Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A. J Thromb Haemost 2007 5 (2) 263-265
    • (2007) J Thromb Haemost , vol.5 , Issue.2 , pp. 263-265
    • Astermark, J.1    Wang, X.2    Oldenburg, J.3    Berntorp, E.4    Lefvert, A.K.5
  • 44
    • 22744433296 scopus 로고    scopus 로고
    • Haemophilia Inhibitor Genetics Studyevaluation of a model for studies of complex diseases using linkage and association methods
    • Hemophilia Inhibitor Genetics Study
    • Berntorp E, Astermark J, Donfield S M. et al, Hemophilia Inhibitor Genetics Study. Haemophilia Inhibitor Genetics Studyevaluation of a model for studies of complex diseases using linkage and association methods. Haemophilia 2005 11 (4) 427-429
    • (2005) Haemophilia , vol.11 , Issue.4 , pp. 427-429
    • Berntorp, E.1    Astermark, J.2    Donfield, S.M.3
  • 45
    • 0034994489 scopus 로고    scopus 로고
    • Incidence of factor VIII inhibitors in severe haemophilia: The importance of patient age
    • Lorenzo J I., Lpez A, Altisent C, Aznar J A. Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient age. Br J Haematol 2001 113 (3) 600-603
    • (2001) Br J Haematol , vol.113 , Issue.3 , pp. 600-603
    • Lorenzo, J.I.1    Lpez, A.2    Altisent, C.3    Aznar, J.A.4
  • 47
    • 33846922841 scopus 로고    scopus 로고
    • Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A
    • Paediatric Working Party of UKHCDO
    • Chalmers E A., Brown S A., Keeling D et al, Paediatric Working Party of UKHCDO. Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A. Haemophilia 2007 13 (2) 149-155
    • (2007) Haemophilia , vol.13 , Issue.2 , pp. 149-155
    • Chalmers, E.A.1    Brown, S.A.2    Keeling, D.3
  • 48
    • 24944440876 scopus 로고    scopus 로고
    • Environmental risk factors for inhibitor development in children with haemophilia A: A case-control study
    • Santagostino E, Mancuso M E., Rocino A et al. Environmental risk factors for inhibitor development in children with haemophilia A: a case-control study. Br J Haematol 2005 130 (3) 422-427
    • (2005) Br J Haematol , vol.130 , Issue.3 , pp. 422-427
    • Santagostino, E.1    Mancuso, M.E.2    Rocino, A.3
  • 49
    • 34250708408 scopus 로고    scopus 로고
    • Treatment characteristics and the risk of inhibitor development: A multicenter cohort study among previously untreated patients with severe hemophilia A
    • Gouw S C., van den Berg H M., le Cessie S, van der Bom J G. Treatment characteristics and the risk of inhibitor development: a multicenter cohort study among previously untreated patients with severe hemophilia A. J Thromb Haemost 2007 5 (7) 1383-1390
    • (2007) J Thromb Haemost , vol.5 , Issue.7 , pp. 1383-1390
    • Gouw, S.C.1    Van Den Berg, H.M.2    Le Cessie, S.3    Van Der Bom, J.G.4
  • 50
    • 34249690732 scopus 로고    scopus 로고
    • Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: The CANAL cohort study
    • Gouw S C., van der Bom J G., Marijke van den Berg H. Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: the CANAL cohort study. Blood 2007 109 (11) 4648-4654
    • (2007) Blood , vol.109 , Issue.11 , pp. 4648-4654
    • Gouw, S.C.1    Van Der Bom, J.G.2    Marijke Van Den Berg, H.3
  • 51
    • 0028201732 scopus 로고
    • Tolerance, danger, and the extended family
    • Matzinger P. Tolerance, danger, and the extended family. Annu Rev Immunol 1994 12 991-1045
    • (1994) Annu Rev Immunol , vol.12 , pp. 991-1045
    • Matzinger, P.1
  • 53
    • 0035903326 scopus 로고    scopus 로고
    • Dendritic cells induce peripheral T cell unresponsiveness under steady state conditions in vivo
    • Hawiger D, Inaba K, Dorsett Y et al. Dendritic cells induce peripheral T cell unresponsiveness under steady state conditions in vivo. J Exp Med 2001 194 (6) 769-779
    • (2001) J Exp Med , vol.194 , Issue.6 , pp. 769-779
    • Hawiger, D.1    Inaba, K.2    Dorsett, Y.3
  • 54
    • 0027394923 scopus 로고
    • A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in the Netherlands
    • Dutch Hemophilia Study Group
    • Rosendaal F R., Nieuwenhuis H K., van den Berg H M. et al, Dutch Hemophilia Study Group. A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in The Netherlands. Blood 1993 81 (8) 2180-2186
    • (1993) Blood , vol.81 , Issue.8 , pp. 2180-2186
    • Rosendaal, F.R.1    Nieuwenhuis, H.K.2    Van Den Berg, H.M.3
  • 55
    • 0027392864 scopus 로고
    • A higher than expected incidence of factor VIII inhibitors in multitransfused haemophilia A patients treated with an intermediate purity pasteurized factor VIII concentrate
    • Peerlinck K, Arnout J, Gilles J G., Saint-Remy J M., Vermylen J. A higher than expected incidence of factor VIII inhibitors in multitransfused haemophilia A patients treated with an intermediate purity pasteurized factor VIII concentrate. Thromb Haemost 1993 69 (2) 115-118
    • (1993) Thromb Haemost , vol.69 , Issue.2 , pp. 115-118
    • Peerlinck, K.1    Arnout, J.2    Gilles, J.G.3    Saint-Remy, J.M.4    Vermylen, J.5
  • 56
    • 0028244702 scopus 로고
    • Clinical course of factor VIII inhibitors developed after exposure to a pasteurised Dutch concentrate compared to classic inhibitors in hemophilia A
    • Mauser-Bunschoten E P., Rosendaal F R., Nieuwenhuis H K., Roosendaal G, Brit E, van den Berg H M. Clinical course of factor VIII inhibitors developed after exposure to a pasteurised Dutch concentrate compared to classic inhibitors in hemophilia A. Thromb Haemost 1994 71 (6) 703-706
    • (1994) Thromb Haemost , vol.71 , Issue.6 , pp. 703-706
    • Mauser-Bunschoten, E.P.1    Rosendaal, F.R.2    Nieuwenhuis, H.K.3    Roosendaal, G.4    Brit, E.5    Van Den Berg, H.M.6
  • 57
    • 0028276140 scopus 로고
    • Inhibitors in hemophilia A: Are some products safer?
    • Brit E, Rosendaal F R. Inhibitors in hemophilia A: are some products safer? Semin Hematol 1994 31 (2, suppl 4) 11-15
    • (1994) Semin Hematol , vol.31 , Issue.SUPPL 4 , pp. 11-15
    • Brit, E.1    Rosendaal, F.R.2
  • 58
    • 1542301024 scopus 로고    scopus 로고
    • Reported inhibitor incidence in FVIII PUP studies: Comparing apples with oranges?
    • Scharrer I, Ehrlich H J. Reported inhibitor incidence in FVIII PUP studies: comparing apples with oranges? Haemophilia 2004 10 (2) 197-198
    • (2004) Haemophilia , vol.10 , Issue.2 , pp. 197-198
    • Scharrer, I.1    Ehrlich, H.J.2
  • 59
    • 33751010515 scopus 로고    scopus 로고
    • Recombinant vs. plasma-derived products, especially those with intact VWF, regarding inhibitor development
    • Ettingshausen C E., Kreuz W. Recombinant vs. plasma-derived products, especially those with intact VWF, regarding inhibitor development. Haemophilia 2006 12 (suppl 6) 102-106
    • (2006) Haemophilia , vol.12 , Issue.SUPPL 6 , pp. 102-106
    • Ettingshausen, C.E.1    Kreuz, W.2
  • 60
    • 3042585962 scopus 로고    scopus 로고
    • Epidemiology of inhibitors and current treatment strategies
    • Kreuz W, Ettingshausen C E., Auerswald G, et al. Epidemiology of inhibitors and current treatment strategies. Haematologica 2003 88 (6) EREP04
    • (2003) Haematologica , vol.88 , Issue.6 , pp. 04
    • Kreuz, W.1    Ettingshausen, C.E.2    Auerswald, G.3
  • 61
    • 30344434999 scopus 로고    scopus 로고
    • Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A
    • FVIII-LFB and Recombinant FVIII study groups
    • Goudemand J, Rothschild C, Demiguel V et al, FVIII-LFB and Recombinant FVIII study groups. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A. Blood 2006 107 (1) 46-51
    • (2006) Blood , vol.107 , Issue.1 , pp. 46-51
    • Goudemand, J.1    Rothschild, C.2    Demiguel, V.3
  • 62
    • 34249711370 scopus 로고    scopus 로고
    • Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: The CANAL cohort study
    • Gouw S C., van der Bom J G., Auerswald G, Ettinghausen C E., Tedgrd U, van den Berg H M. Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study. Blood 2007 109 (11) 4693-4697
    • (2007) Blood , vol.109 , Issue.11 , pp. 4693-4697
    • Gouw, S.C.1    Van Der Bom, J.G.2    Auerswald, G.3    Ettinghausen, C.E.4    Tedgrd, U.5    Van Den Berg, H.M.6
  • 63
    • 0029910889 scopus 로고    scopus 로고
    • Factor VIII inhibitor antibodies with C2 domain specificity are less inhibitory to factor VIII complexed with von Willebrand factor
    • Suzuki T, Arai M, Amano K, Kagawa K, Fukutake K. Factor VIII inhibitor antibodies with C2 domain specificity are less inhibitory to factor VIII complexed with von Willebrand factor. Thromb Haemost 1996 76 (5) 749-754
    • (1996) Thromb Haemost , vol.76 , Issue.5 , pp. 749-754
    • Suzuki, T.1    Arai, M.2    Amano, K.3    Kagawa, K.4    Fukutake, K.5
  • 64
  • 65
    • 33846244931 scopus 로고    scopus 로고
    • VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors
    • Dasgupta S, Repess Y, Bayry J et al. VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors. Blood 2007 109 (2) 610-612
    • (2007) Blood , vol.109 , Issue.2 , pp. 610-612
    • Dasgupta, S.1    Repess, Y.2    Bayry, J.3
  • 66
    • 0028000681 scopus 로고
    • Identification of transforming growth factor-beta as a contaminant in factor VIII concentrates: A possible link with immunosuppressive effects in hemophiliacs
    • Wadhwa M, Dilger P, Tubbs J, Mire-Sluis A, Barrowcliffe T, Thorpe R. Identification of transforming growth factor-beta as a contaminant in factor VIII concentrates: a possible link with immunosuppressive effects in hemophiliacs. Blood 1994 84 (6) 2021-2030
    • (1994) Blood , vol.84 , Issue.6 , pp. 2021-2030
    • Wadhwa, M.1    Dilger, P.2    Tubbs, J.3    Mire-Sluis, A.4    Barrowcliffe, T.5    Thorpe, R.6
  • 67
    • 0034116888 scopus 로고    scopus 로고
    • Effect of factor VIII concentrate on antigen-presenting cell (APC)/T-cell interactions in vitro: Relevance to inhibitor formation and tolerance induction
    • Hodge G, Han P. Effect of factor VIII concentrate on antigen-presenting cell (APC)/T-cell interactions in vitro: relevance to inhibitor formation and tolerance induction. Br J Haematol 2000 109 (1) 195-200
    • (2000) Br J Haematol , vol.109 , Issue.1 , pp. 195-200
    • Hodge, G.1    Han, P.2
  • 68
    • 0032853816 scopus 로고    scopus 로고
    • Effect of factor VIII concentrate on leucocyte cytokine production: Characterization of TGF-beta as an immunomodulatory component in plasma-derived factor VIII concentrate
    • Hodge G, Flower R, Han P. Effect of factor VIII concentrate on leucocyte cytokine production: characterization of TGF-beta as an immunomodulatory component in plasma-derived factor VIII concentrate. Br J Haematol 1999 106 (3) 784-791
    • (1999) Br J Haematol , vol.106 , Issue.3 , pp. 784-791
    • Hodge, G.1    Flower, R.2    Han, P.3
  • 69
    • 0031048881 scopus 로고    scopus 로고
    • Factor VIII inhibitors in previously treated haemophilia A patients with a double virus-inactivated plasma derived factor VIII concentrate
    • Peerlinck K, Arnout J, Di Giambattista M et al. Factor VIII inhibitors in previously treated haemophilia A patients with a double virus-inactivated plasma derived factor VIII concentrate. Thromb Haemost 1997 77 (1) 80-86
    • (1997) Thromb Haemost , vol.77 , Issue.1 , pp. 80-86
    • Peerlinck, K.1    Arnout, J.2    Di Giambattista, M.3
  • 70
    • 0032750777 scopus 로고    scopus 로고
    • Phospholipid binding of factor VIII in different therapeutic concentrates
    • Raut S, Weller L, Barrowcliffe T W. Phospholipid binding of factor VIII in different therapeutic concentrates. Br J Haematol 1999 107 (2) 323-329
    • (1999) Br J Haematol , vol.107 , Issue.2 , pp. 323-329
    • Raut, S.1    Weller, L.2    Barrowcliffe, T.W.3
  • 71
    • 0001338374 scopus 로고    scopus 로고
    • Factor VIII inhibitors on a DS-treated and pasteurized concentrate associated with specific batches and batch characteristics
    • Abstract OC-2407
    • Rosendaal F R. Factor VIII inhibitors on a DS-treated and pasteurized concentrate associated with specific batches and batch characteristics. Thromb Haemost 1997 77 590 Abstract OC-2407
    • (1997) Thromb Haemost , vol.77 , pp. 590
    • Rosendaal, F.R.1
  • 72
    • 37149022850 scopus 로고    scopus 로고
    • Factor VIII products and inhibitor development: The SIPPET study (survey of inhibitors in plasma-product exposed toddlers)
    • Mannucci P M., Gringeri A, Peyvandi F, Santagostino E. Factor VIII products and inhibitor development: the SIPPET study (survey of inhibitors in plasma-product exposed toddlers). Haemophilia 2007 13 (suppl 5) 65-68
    • (2007) Haemophilia , vol.13 , Issue.SUPPL 5 , pp. 65-68
    • Mannucci, P.M.1    Gringeri, A.2    Peyvandi, F.3    Santagostino, E.4
  • 73
    • 0031792547 scopus 로고    scopus 로고
    • Is a change of factor VIII product a risk factor for the development of a factor VIII inhibitor?
    • Baglin T, Beacham E. Is a change of factor VIII product a risk factor for the development of a factor VIII inhibitor? Thromb Haemost 1998 80 (6) 1036-1037
    • (1998) Thromb Haemost , vol.80 , Issue.6 , pp. 1036-1037
    • Baglin, T.1    Beacham, E.2
  • 74
    • 25444445056 scopus 로고    scopus 로고
    • Inhibitor development in patients with hemophilia A after continuous infusion of FVIII concentrates
    • von Auer C, Oldenburg J, von Depka M et al. Inhibitor development in patients with hemophilia A after continuous infusion of FVIII concentrates. Ann N Y Acad Sci 2005 1051 498-505
    • (2005) Ann N y Acad Sci , vol.1051 , pp. 498-505
    • Von Auer, C.1    Oldenburg, J.2    Von Depka, M.3
  • 75
    • 0033832945 scopus 로고    scopus 로고
    • Oral immune tolerance induction to factor VIII via breast milk, a possibility?
    • Yee T T., Lee C A. Oral immune tolerance induction to factor VIII via breast milk, a possibility? Haemophilia 2000 6 (5) 591
    • (2000) Haemophilia , vol.6 , Issue.5 , pp. 591
    • Yee, T.T.1    Lee, C.A.2
  • 76
    • 25444458653 scopus 로고    scopus 로고
    • No protective effect of breastfeeding on inhibitor formation in severe hemophilia
    • Jansen I M., Fischer K, Van Der Bom J G., Van Den Berg H M. No protective effect of breastfeeding on inhibitor formation in severe hemophilia. Pediatr Hematol Oncol 2005 22 (7) 575-580
    • (2005) Pediatr Hematol Oncol , vol.22 , Issue.7 , pp. 575-580
    • Jansen, I.M.1    Fischer, K.2    Van Der Bom, J.G.3    Van Den Berg, H.M.4
  • 77
    • 0036735251 scopus 로고    scopus 로고
    • Breastfeeding does not influence the development of inhibitors in haemophilia
    • Knobe K E., Tengborn L I., Petrini P, Ljung R C. Breastfeeding does not influence the development of inhibitors in haemophilia. Haemophilia 2002 8 (5) 657-659
    • (2002) Haemophilia , vol.8 , Issue.5 , pp. 657-659
    • Knobe, K.E.1    Tengborn, L.I.2    Petrini, P.3    Ljung, R.C.4
  • 78
    • 0023856830 scopus 로고
    • The natural history of factor VIII:C inhibitors in patients with hemophilia A: A national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors
    • McMillan C W., Shapiro S S., Whitehurst D, Hoyer L W., Rao A V., Lazerson J. The natural history of factor VIII:C inhibitors in patients with hemophilia A: a national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors. Blood 1988 71 (2) 344-348
    • (1988) Blood , vol.71 , Issue.2 , pp. 344-348
    • McMillan, C.W.1    Shapiro, S.S.2    Whitehurst, D.3    Hoyer, L.W.4    Rao, A.V.5    Lazerson, J.6
  • 79
    • 65449147630 scopus 로고    scopus 로고
    • A case control study to examine treatment related factors in the development of inhibitors in haemophilia A
    • Maclean P, Young D, Chalmers E. A case control study to examine treatment related factors in the development of inhibitors in haemophilia A. Haemophilia 2008 14 (Suppl 2) 44
    • (2008) Haemophilia , vol.14 , Issue.SUPPL 2 , pp. 44
    • MacLean, P.1    Young, D.2    Chalmers, E.3
  • 80
    • 0032883366 scopus 로고    scopus 로고
    • Induction of immune tolerance in haemophilia A inhibitor patients by the Bonn Protocol: Predictive parameter for therapy duration and outcome
    • Oldenburg J, Schwaab R, Brackmann H H. Induction of immune tolerance in haemophilia A inhibitor patients by the Bonn Protocol: predictive parameter for therapy duration and outcome. Vox Sang 1999 77 (Suppl 1) 49-54
    • (1999) Vox Sang , vol.77 , Issue.SUPPL 1 , pp. 49-54
    • Oldenburg, J.1    Schwaab, R.2    Brackmann, H.H.3
  • 81
    • 33748743730 scopus 로고    scopus 로고
    • The international immune tolerance study: A multicenter prospective randomized trial in progress
    • Dimichele D M., Hay C R. The international immune tolerance study: a multicenter prospective randomized trial in progress. J Thromb Haemost 2006 4 (10) 2271-2273
    • (2006) J Thromb Haemost , vol.4 , Issue.10 , pp. 2271-2273
    • Dimichele, D.M.1    Hay, C.R.2
  • 82
    • 71649095495 scopus 로고    scopus 로고
    • Effect of route of administration of human recombinant factor VIII on its immunogenicity in hemophilia A mice
    • Peng A, Gaitonde P, Kosloski M P. et al. Effect of route of administration of human recombinant factor VIII on its immunogenicity in hemophilia A mice. J Pharm Sci 2009 98 (12) 4480-4484
    • (2009) J Pharm Sci , vol.98 , Issue.12 , pp. 4480-4484
    • Peng, A.1    Gaitonde, P.2    Kosloski, M.P.3
  • 83
    • 56749175272 scopus 로고    scopus 로고
    • Risk stratification for inhibitor development at first treatment for severe hemophilia A: A tool for clinical practice
    • Ter Avest P C., Fischer K, Mancuso M E. et al. Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice. J Thromb Haemost 2008 6 (12) 2048-2054
    • (2008) J Thromb Haemost , vol.6 , Issue.12 , pp. 2048-2054
    • Ter Avest, P.C.1    Fischer, K.2    Mancuso, M.E.3
  • 84
    • 34548308950 scopus 로고    scopus 로고
    • Meeting report: Ninth and tenth workshops of the European Paediatric Network for Haemophilia Management (PedNet)
    • European Paediatric Network for Haemophilia Management (PedNet)
    • Kurnik K, Thomas A E., European Paediatric Network for Haemophilia Management (PedNet). Meeting report: ninth and tenth workshops of the European Paediatric Network for Haemophilia Management (PedNet). Haemophilia 2007 13 (5) 658-662
    • (2007) Haemophilia , vol.13 , Issue.5 , pp. 658-662
    • Kurnik, K.1    Thomas, A.E.2
  • 85
    • 0035655711 scopus 로고    scopus 로고
    • Blockade of CD40/CD40 ligand interactions prevents induction of factor VIII inhibitors in hemophilic mice but does not induce lasting immune tolerance
    • Reipert B M., Sasgary M, Ahmad R U., Auer W, Turecek P L., Schwarz H P. Blockade of CD40/CD40 ligand interactions prevents induction of factor VIII inhibitors in hemophilic mice but does not induce lasting immune tolerance. Thromb Haemost 2001 86 (6) 1345-1352
    • (2001) Thromb Haemost , vol.86 , Issue.6 , pp. 1345-1352
    • Reipert, B.M.1    Sasgary, M.2    Ahmad, R.U.3    Auer, W.4    Turecek, P.L.5    Schwarz, H.P.6
  • 86
    • 0034651552 scopus 로고    scopus 로고
    • Prevention and treatment of factor VIII inhibitors in murine hemophilia A
    • Qian J, Collins M, Sharpe A H., Hoyer L W. Prevention and treatment of factor VIII inhibitors in murine hemophilia A. Blood 2000 95 (4) 1324-1329
    • (2000) Blood , vol.95 , Issue.4 , pp. 1324-1329
    • Qian, J.1    Collins, M.2    Sharpe, A.H.3    Hoyer, L.W.4
  • 87
    • 52649172605 scopus 로고    scopus 로고
    • Transient blockade of the inducible costimulator pathway generates long-term tolerance to factor VIII after nonviral gene transfer into hemophilia A mice
    • Peng B, Ye P, Blazar B R. et al. Transient blockade of the inducible costimulator pathway generates long-term tolerance to factor VIII after nonviral gene transfer into hemophilia A mice. Blood 2008 112 (5) 1662-1672
    • (2008) Blood , vol.112 , Issue.5 , pp. 1662-1672
    • Peng, B.1    Ye, P.2    Blazar, B.R.3
  • 88
    • 56749158179 scopus 로고    scopus 로고
    • Reduction of the immune response to factor VIII mediated through tolerogenic factor VIII presentation by immature dendritic cells
    • Qadura M, Othman M, Waters B et al. Reduction of the immune response to factor VIII mediated through tolerogenic factor VIII presentation by immature dendritic cells. J Thromb Haemost 2008 6 (12) 2095-2104
    • (2008) J Thromb Haemost , vol.6 , Issue.12 , pp. 2095-2104
    • Qadura, M.1    Othman, M.2    Waters, B.3
  • 89
    • 59449102416 scopus 로고    scopus 로고
    • Anti-CD3 prevents factor VIII inhibitor development in hemophilia A mice by a regulatory CD4+CD25+-dependent mechanism and by shifting cytokine production to favor a Th1 response
    • Waters B, Qadura M, Burnett E et al. Anti-CD3 prevents factor VIII inhibitor development in hemophilia A mice by a regulatory CD4+CD25+-dependent mechanism and by shifting cytokine production to favor a Th1 response. Blood 2009 113 (1) 193-203
    • (2009) Blood , vol.113 , Issue.1 , pp. 193-203
    • Waters, B.1    Qadura, M.2    Burnett, E.3
  • 90
    • 20444476217 scopus 로고    scopus 로고
    • Induction of tolerance to factor VIII inhibitors by gene therapy with immunodominant A2 and C2 domains presented by B cells as Ig fusion proteins
    • Lei T C., Scott D W. Induction of tolerance to factor VIII inhibitors by gene therapy with immunodominant A2 and C2 domains presented by B cells as Ig fusion proteins. Blood 2005 105 (12) 4865-4870
    • (2005) Blood , vol.105 , Issue.12 , pp. 4865-4870
    • Lei, T.C.1    Scott, D.W.2
  • 91
    • 0036861899 scopus 로고    scopus 로고
    • Immunogenicity of therapeutic proteins: Clinical implications and future prospects
    • Schellekens H. Immunogenicity of therapeutic proteins: clinical implications and future prospects. Clin Ther 2002 24 (11) 1720-1740, discussion 1719
    • (2002) Clin Ther , vol.24 , Issue.11 , pp. 1720-1740
    • Schellekens, H.1
  • 92
    • 34547430130 scopus 로고    scopus 로고
    • A role for exposed mannosylations in presentation of human therapeutic self-proteins to CD4+T lymphocytes
    • Dasgupta S, Navarrete A M., Bayry J et al. A role for exposed mannosylations in presentation of human therapeutic self-proteins to CD4+T lymphocytes. Proc Natl Acad Sci U S A 2007 104 (21) 8965-8970
    • (2007) Proc Natl Acad Sci U S A , vol.104 , Issue.21 , pp. 8965-8970
    • Dasgupta, S.1    Navarrete, A.M.2    Bayry, J.3
  • 93
    • 67849128717 scopus 로고    scopus 로고
    • Clinical prediction models for inhibitor development in severe hemophilia A
    • van den Berg H M., Chalmers E A. Clinical prediction models for inhibitor development in severe hemophilia A. J Thromb Haemost 2009 7 (Suppl 1) 98-102
    • (2009) J Thromb Haemost , vol.7 , Issue.SUPPL 1 , pp. 98-102
    • Van Den Berg, H.M.1    Chalmers, E.A.2
  • 94
    • 0031958313 scopus 로고    scopus 로고
    • Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation
    • Hay C R., Ludlam C A., Colvin B T. et al. Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation. Thromb Haemost 1998 79 (4) 762-766
    • (1998) Thromb Haemost , vol.79 , Issue.4 , pp. 762-766
    • Hay, C.R.1    Ludlam, C.A.2    Colvin, B.T.3
  • 95
    • 0031804517 scopus 로고    scopus 로고
    • The factor VIII Structure and Mutation Resource Site: HAMSTeRS version 4
    • Kemball-Cook G, Tuddenham E G., Wacey A I. The factor VIII Structure and Mutation Resource Site: HAMSTeRS version 4. Nucleic Acids Res 1998 26 (1) 216-219
    • (1998) Nucleic Acids Res , vol.26 , Issue.1 , pp. 216-219
    • Kemball-Cook, G.1    Tuddenham, E.G.2    Wacey, A.I.3
  • 96
    • 44249088320 scopus 로고    scopus 로고
    • Mild/moderate haemophilia A: New insights into molecular mechanisms and inhibitor development
    • D'Oiron R, Pipe S W., Jacquemin M. Mild/moderate haemophilia A: new insights into molecular mechanisms and inhibitor development. Haemophilia 2008 14 (Suppl 3) 138-146
    • (2008) Haemophilia , vol.14 , Issue.SUPPL 3 , pp. 138-146
    • D'Oiron, R.1    Pipe, S.W.2    Jacquemin, M.3
  • 97
    • 0842333021 scopus 로고    scopus 로고
    • Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A
    • Sharathkumar A, Lillicrap D, Blanchette V S. et al. Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A. J Thromb Haemost 2003 1 (6) 1228-1236
    • (2003) J Thromb Haemost , vol.1 , Issue.6 , pp. 1228-1236
    • Sharathkumar, A.1    Lillicrap, D.2    Blanchette, V.S.3
  • 98
    • 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 hemophilia A
    • Eckhardt C L., Menke L A., van Ommen C H. et al. Intensive peri-operative use of factor VIII and the Arg593>Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A. J Thromb Haemost 2009 7 (6) 930-937
    • (2009) J Thromb Haemost , vol.7 , Issue.6 , pp. 930-937
    • Eckhardt, C.L.1    Menke, L.A.2    Van Ommen, C.H.3
  • 99
    • 20344372906 scopus 로고    scopus 로고
    • Molecular genotyping of the Italian cohort of patients with hemophilia B
    • AICE HB Study Group
    • Belvini D, Salviato R, Radossi P et al, AICE HB Study Group. Molecular genotyping of the Italian cohort of patients with hemophilia B. Haematologica 2005 90 (5) 635-642
    • (2005) Haematologica , vol.90 , Issue.5 , pp. 635-642
    • Belvini, D.1    Salviato, R.2    Radossi, P.3
  • 100
    • 69949092766 scopus 로고    scopus 로고
    • Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (19972006)
    • Chitlur M, Warrier I, Rajpurkar M, Lusher J M. Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (19972006). Haemophilia 2009 15 (5) 1027-1031
    • (2009) Haemophilia , vol.15 , Issue.5 , pp. 1027-1031
    • Chitlur, M.1    Warrier, I.2    Rajpurkar, M.3    Lusher, J.M.4
  • 101
    • 6544277992 scopus 로고    scopus 로고
    • Anaphylactic response to factor IX replacement therapy in haemophilia B patients: Complete gene deletions confer the highest risk
    • Thorland E C., Drost J B., Lusher J M. et al. Anaphylactic response to factor IX replacement therapy in haemophilia B patients: complete gene deletions confer the highest risk. Haemophilia 1999 5 (2) 101-105
    • (1999) Haemophilia , vol.5 , Issue.2 , pp. 101-105
    • Thorland, E.C.1    Drost, J.B.2    Lusher, J.M.3
  • 102


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