Structure of a factor VIIIC2 domain-immunoglobulin G4κ Fab complex:: identification of an inhibitory antibody epitope on the surface of factor VIII

被引:126
作者
Spiegel, PC
Jacquemin, M
Saint-Remy, JMR
Stoddard, BL
Pratt, KP
机构
[1] Katholieke Univ Leuven, Ctr Mol & Vasc Biol, Louvain, Belgium
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[3] Univ Washington, Grad Program Biomol Struct & Design, Seattle, WA 98195 USA
关键词
D O I
10.1182/blood.V98.1.13
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The development of an immune response to infused factor VIII is a complication affecting many patients with hemophilia A. Inhibitor antibodies bind to antigenic determinants on the factor VIII molecule and block its procoagulant activity. A patient-derived inhibitory immunoglobulin G4 kappa antibody (BO2C11) produced by an immortalized memory B-lymphocyte cell line interferes with the binding of factor VIII to phospholipid surfaces and to von Willebrand factor, The structure of a Fab fragment derived from this antibody complexed with the factor VIII C2 domain was determined at 2.0 Angstrom resolution, The Fab interacts with solvent-exposed basic and hydrophobic side chains that form a membrane-association surface of factor VIII, This atomic resolution structure suggests a variety of amino acid substitutions in the C2 domain of factor VIII that might prevent the binding of anti-C2 inhibitor antibodies without significantly compromising the procoagulant functions of factor VIII.(C) 2001 by The American Society of Hematology.
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页码:13 / 19
页数:7
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