메뉴 건너뛰기




Volumn 75, Issue 3, 1997, Pages 111-115

Alloantibody from a patient with severe von Willebrand disease inhibits von Willebrand factor-FVIII interaction

Author keywords

Alloantibody; FVIII; FVIII binding; Inhibitor; vWF

Indexed keywords

ALLOANTIBODY; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 INHIBITOR; IMMUNOGLOBULIN G; MONOCLONAL ANTIBODY; POLYCLONAL ANTIBODY; VON WILLEBRAND FACTOR;

EID: 14444274587     PISSN: 09395555     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002770050323     Document Type: Article
Times cited : (9)

References (25)
  • 2
    • 0024400371 scopus 로고
    • A monoclonal antibody to von Willebrand factor (vWF) inhibits factor VIII binding. Localization of its antigenic determinant to a nonadecapeptide at the amino terminus of the mature vWF polypeptide
    • Bahou WF, Ginsburg D, Sikkink R, Litwiller R, Pass DN (1991) A monoclonal antibody to von Willebrand factor (vWF) inhibits factor VIII binding. Localization of its antigenic determinant to a nonadecapeptide at the amino terminus of the mature vWF polypeptide. J Clin Invest 84:56-61
    • (1991) J Clin Invest , vol.84 , pp. 56-61
    • Bahou, W.F.1    Ginsburg, D.2    Sikkink, R.3    Litwiller, R.4    Pass, D.N.5
  • 5
    • 14444282164 scopus 로고
    • An alloantibody to von Willebrand factor selectively inhibiting the binding of von Willebrand factor to collagen in a patient with severe von Willebrand disease
    • abstract
    • Budde U, Effenberg W, Oldenburg J, Schneppenheim R, van Genderen P, Drewke E, Brackmann HH (1995) An alloantibody to von Willebrand factor selectively inhibiting the binding of von Willebrand factor to collagen in a patient with severe von Willebrand disease. Thromb Haemost 73:1161 (abstract)
    • (1995) Thromb Haemost , vol.73 , pp. 1161
    • Budde, U.1    Effenberg, W.2    Oldenburg, J.3    Schneppenheim, R.4    Van Genderen, P.5    Drewke, E.6    Brackmann, H.H.7
  • 6
    • 0023217139 scopus 로고
    • A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor
    • Foster PA, Fulcher CA, Marti T, Titani K, Zimmerman TS (1987) A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor. J Biol Chem 262:8443-8446
    • (1987) J Biol Chem , vol.262 , pp. 8443-8446
    • Foster, P.A.1    Fulcher, C.A.2    Marti, T.3    Titani, K.4    Zimmerman, T.S.5
  • 7
    • 0025308680 scopus 로고
    • A synthetic factor VIII peptide of eight amino acid residues (1677-1684) contains the binding region of an anti-factor VIII antibody which inhibits the binding of factor VIII to von Willebrand factor
    • Foster PA, Fulcher CA, Hounghten RA, Zimmerman TS (1990) A synthetic factor VIII peptide of eight amino acid residues (1677-1684) contains the binding region of an anti-factor VIII antibody which inhibits the binding of factor VIII to von Willebrand factor. Thromb Haemost 63:403-406
    • (1990) Thromb Haemost , vol.63 , pp. 403-406
    • Foster, P.A.1    Fulcher, C.A.2    Hounghten, R.A.3    Zimmerman, T.S.4
  • 8
    • 1642595858 scopus 로고
    • Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody
    • Fulcher CA, Zimmerman TS (1982) Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody. Proc Natl Acad Sci USA 79:1648-1652
    • (1982) Proc Natl Acad Sci USA , vol.79 , pp. 1648-1652
    • Fulcher, C.A.1    Zimmerman, T.S.2
  • 10
    • 0008919266 scopus 로고
    • Apparent IgG anti-factor VIII antibodies in normal individuals are specific for ABO blood group substances
    • abstract
    • Gill JC, Stephany K, Newton-Nash D, Foster PA (1995) Apparent IgG anti-factor VIII antibodies in normal individuals are specific for ABO blood group substances. Blood 86:611a (abstract)
    • (1995) Blood , vol.86
    • Gill, J.C.1    Stephany, K.2    Newton-Nash, D.3    Foster, P.A.4
  • 11
    • 14444268244 scopus 로고
    • Replacement therapy for surgery in type III von Willebrand patient with inhibitors to factor VIII procoagulant
    • abstract
    • Hanna WT (1989) Replacement therapy for surgery in type III von Willebrand patient with inhibitors to factor VIII procoagulant. Thromb Haemost 62:224 (abstract)
    • (1989) Thromb Haemost , vol.62 , pp. 224
    • Hanna, W.T.1
  • 13
    • 0025755871 scopus 로고
    • Production and characterization of recombinant factor VIII
    • Klein U (1991) Production and characterization of recombinant factor VIII. Semin Hematol 28 [Suppl 1]: 17-21
    • (1991) Semin Hematol , vol.28 , Issue.1 SUPPL. , pp. 17-21
    • Klein, U.1
  • 14
    • 0023722544 scopus 로고
    • Further specificity characterization of von Willebrand factor inhibitors developed in two patients with severe von Willebrand disease
    • López Fernández MF, Martín R, López Berges C, Ramos F, de Bosch N, Batlle J (1988) Further specificity characterization of von Willebrand factor inhibitors developed in two patients with severe von Willebrand disease. Blood 72:116-120
    • (1988) Blood , vol.72 , pp. 116-120
    • López Fernández, M.F.1    Martín, R.2    López Berges, C.3    Ramos, F.4    De Bosch, N.5    Batlle, J.6
  • 15
    • 0026562062 scopus 로고
    • Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII
    • López Fernández MF, Blanco López MJ, Castiñeira MP, Batlle J (1992) Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. Am J Hematol 40:20-27
    • (1992) Am J Hematol , vol.40 , pp. 20-27
    • López Fernández, M.F.1    Blanco López, M.J.2    Castiñeira, M.P.3    Batlle, J.4
  • 17
    • 0025012865 scopus 로고
    • A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction
    • Mazurier C, Dieval J, Jorieux S, Delobel J, Goudemand M (1990) A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction. Blood 75:20-26
    • (1990) Blood , vol.75 , pp. 20-26
    • Mazurier, C.1    Dieval, J.2    Jorieux, S.3    Delobel, J.4    Goudemand, M.5
  • 18
    • 0025116340 scopus 로고
    • Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed as mild hemophilia A and hemophilia A carriers: Consequences for therapy and genetic counselling
    • Mazurier C, Gaucher C, Jorieux S, Parquet-Gernez A, Goudemand M (1990) Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed as mild hemophilia A and hemophilia A carriers: consequences for therapy and genetic counselling. Br J Haematol 76:372-379
    • (1990) Br J Haematol , vol.76 , pp. 372-379
    • Mazurier, C.1    Gaucher, C.2    Jorieux, S.3    Parquet-Gernez, A.4    Goudemand, M.5
  • 19
    • 0024425034 scopus 로고
    • New variant of von Willebrand disease with defective binding to factor VIII
    • Nishino M, Girma JP, Rothschild C, Fressinaud E, Meyer D (1989) New variant of von Willebrand disease with defective binding to factor VIII. Blood 74:1591-1599
    • (1989) Blood , vol.74 , pp. 1591-1599
    • Nishino, M.1    Girma, J.P.2    Rothschild, C.3    Fressinaud, E.4    Meyer, D.5
  • 20
    • 84995217166 scopus 로고
    • A case of recessive type 2N von Willebrand's disease due to Arg 53 Trp substitution
    • Pérez Casai M, Daily M, Peake I, Batlle J (1995) A case of recessive type 2N von Willebrand's disease due to Arg 53 Trp substitution. Am J Hematol 48:140
    • (1995) Am J Hematol , vol.48 , pp. 140
    • Pérez Casai, M.1    Daily, M.2    Peake, I.3    Batlle, J.4
  • 21
    • 0026766155 scopus 로고
    • The structure and function of von Willebrand factor
    • Ruggeri ZM, Ware J (1992) The structure and function of von Willebrand factor. Thromb Haemost 67:594-599
    • (1992) Thromb Haemost , vol.67 , pp. 594-599
    • Ruggeri, Z.M.1    Ware, J.2
  • 23
    • 0021361847 scopus 로고
    • Two distinct forms of factor VIII coagulant protein in human plasma. Cleavage by thrombin and differences in coagulant activity and association with von Willebrand factor
    • Weinstein MJ, Chute LE (1984) Two distinct forms of factor VIII coagulant protein in human plasma. Cleavage by thrombin and differences in coagulant activity and association with von Willebrand factor. J Clin Invest 73:307-316
    • (1984) J Clin Invest , vol.73 , pp. 307-316
    • Weinstein, M.J.1    Chute, L.E.2
  • 24
    • 0017754787 scopus 로고
    • Stabilization of factor VIII in plasma by the von Willebrand factor
    • Weiss HJ, Sussmann II, Hoyer LW (1977) Stabilization of factor VIII in plasma by the von Willebrand factor. J Clin Invest 60:390-404
    • (1977) J Clin Invest , vol.60 , pp. 390-404
    • Weiss, H.J.1    Sussmann, I.I.2    Hoyer, L.W.3
  • 25
    • 0023989138 scopus 로고
    • Purification of factor VIII by monoclonal antibody affinity chromatography
    • Zimmerman TS (1988) Purification of factor VIII by monoclonal antibody affinity chromatography. Semin Hematol 24 [Suppl 1]:25-26
    • (1988) Semin Hematol , vol.24 , Issue.1 SUPPL. , pp. 25-26
    • Zimmerman, T.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.