Kandiah D A, Sheng Y H, Krilis S A
Department of Immunology, Allergy and Infectious Disease, University of New South Wales, St George Hospital, Kogarah, Australia.
Lupus. 1996 Oct;5(5):381-5. doi: 10.1177/096120339600500509.
Antiphospholipid' (aPL) antibodies are of important clinical significance because of their association with thrombosis both arterial and venous, recurrent foetal loss, specific neurological sequelae like seizures and chorea, cardiac valvular abnormalities and thrombocytopenia. Traditionally these autoantibodies have been assayed using phospholipid (PL) dependent tests and are classified as lupus anticoagulants (LA) and anticardiolipin (aCL) antibodies based on the method of detection. The antibodies thus, had been thought to bind PLs but it has now become clear that the true antigens are PL-binding proteins. The major protein consistently found as the target antigen for these autoantibodies is beta 2-glycoprotein I (beta 2-GPI). Other candidate PL-binding proteins have also been investigated including prothrombin, protein C and protein S but thus far appear to play less important roles in the binding of these antibodies.
抗磷脂(aPL)抗体具有重要的临床意义,因为它们与动脉和静脉血栓形成、复发性胎儿丢失、癫痫和舞蹈病等特定神经后遗症、心脏瓣膜异常及血小板减少症相关。传统上,这些自身抗体通过依赖磷脂(PL)的检测方法进行测定,并根据检测方法分为狼疮抗凝物(LA)和抗心磷脂(aCL)抗体。因此,这些抗体曾被认为是与磷脂结合,但现在已经明确真正的抗原是磷脂结合蛋白。一直作为这些自身抗体靶抗原被发现的主要蛋白质是β2-糖蛋白I(β2-GPI)。其他候选的磷脂结合蛋白也已被研究,包括凝血酶原、蛋白C和蛋白S,但迄今为止,它们在这些抗体的结合中似乎发挥着不太重要的作用。