The significance of autoantibodies against β2-glycoprotein I

被引:116
|
作者
de Groot, Philip G. [1 ]
Urbanus, Rolf T. [1 ]
机构
[1] Univ Med Ctr, Dept Clin Chem & Haematol, Utrecht, Netherlands
关键词
LUPUS ANTICOAGULANT ACTIVITY; AUTOIMMUNE ANTIPHOSPHOLIPID ANTIBODIES; INTERNATIONAL CONSENSUS STATEMENT; APOLIPOPROTEIN-E RECEPTOR-2'; ANTI-BETA-2 GLYCOPROTEIN I; TOLL-LIKE RECEPTOR; ANTICARDIOLIPIN ANTIBODIES; DOMAIN-I; ANIONIC PHOSPHOLIPIDS; ENDOTHELIAL-CELLS;
D O I
10.1182/blood-2012-03-378646
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The antiphospholipid syndrome (APS) is defined by the persistent presence of antiphospholipid antibodies in patients with a history of thrombosis and/or pregnancy morbidity, including fetal loss. APS is an autoimmune disease with a confusing name because the pathologic auto-antibodies are shown to be directed against the plasma protein beta(2)-glycoprotein I and not against phospholipids. In fact, autoantibodies that recognize phospholipids themselves are not associated with thrombosis but with infectious diseases. One of the intriguing questions is why autoantibodies against beta(2)-glycoprotein I are so commonly found in both patients and the healthy. Several potential mechanisms have been suggested to explain the increased thrombotic risk in patients with these autoantibodies. In this overview, we will summarize our knowledge on the etiology of the autoantibodies, and we will discuss the evidence that identify autoantibodies against beta(2)-glycoprotein I as the culprit of APS. (Blood. 2012; 120(2):266-274)
引用
收藏
页码:266 / 274
页数:9
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