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因子VIII抑制物抗体的表位特异性及失活机制

Epitope specificity and inactivation mechanisms of factor VIII inhibitor antibodies.

作者信息

Scandella D

机构信息

Holland Laboratory, American Red Cross, Rockville, Md., USA.

出版信息

Vox Sang. 1999;77 Suppl 1:17-20. doi: 10.1159/000056708.

Abstract

The domain specificity of anti-factor VIII (FVIII) inhibitor antibodies was determined in assays using FVIII domains generated by thrombin cleavage or expressed as recombinant polypeptides to neutralise the inhibitor. The results revealed the existence of three major types of inhibitors, and various combinations of these antibodies were found in haemophilic and autoantibody patients. Anti-A2 domain inhibitors prevent normal function of the FVIII/factor IXa (FIXa)/phospholipid complex in an unknown manner. Binding of FVIII to phospholipid and to von Willebrand factor is blocked by anti-C2 domain antibodies, and the binding of FVIII to FIXa is prevented by anti-A3 domain antibodies. A rare type of inhibitor prevents release of activated FVIII from von Willebrand factor (vWf), and another probably interferes with FVIII binding to factor X (FX) because it shares the epitope of a monoclonal antibody with this property.

摘要

通过使用经凝血酶切割产生的FVIII结构域或作为重组多肽表达的FVIII结构域来中和抑制剂的试验,确定了抗因子VIII(FVIII)抑制剂抗体的结构域特异性。结果揭示了三种主要类型抑制剂的存在,并且在血友病患者和自身抗体患者中发现了这些抗体的各种组合。抗A2结构域抑制剂以未知方式阻止FVIII/因子IXa(FIXa)/磷脂复合物的正常功能。抗C2结构域抗体可阻断FVIII与磷脂和血管性血友病因子的结合,抗A3结构域抗体可阻止FVIII与FIXa的结合。一种罕见类型的抑制剂可阻止活化的FVIII从血管性血友病因子(vWf)中释放,另一种抑制剂可能会干扰FVIII与因子X(FX)的结合,因为它与具有该特性的单克隆抗体共享表位。

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