INOVA Diagnostics, INC., San Diego, CA 32131-1638, USA.
Autoimmun Rev. 2012 Dec;12(2):313-7. doi: 10.1016/j.autrev.2012.05.006. Epub 2012 May 28.
Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by frequent clotting in arteries and veins and/or miscarriages. Autoantibodies to phospholipids and to beta 2 glycoprotein 1 (β(2)GP1) play an important role in the pathogenesis of APS. Antibodies to the domain 1 of β(2)GP1 (β(2)GP1-D1) have been suggested as a risk marker for thrombosis and to a lesser extent for pregnancy complications in patients suffering from APS. Despite significant interest in anti-β(2)GP1-D1 antibodies and a considerable research history, the number of studies is still limited and acceptance of the clinical significance of this biomarker is still evolving. The present review summarizes the current knowledge of anti-β(2)GP1-D1 antibodies and provides insights on recent discoveries. Moreover, we present a suggested guideline for future studies to better understand and verify the clinical utility of anti-β(2)GP1-D1 antibodies.
抗磷脂综合征(APS)是一种自身免疫性疾病,其特征是动静脉频繁发生血栓形成和/或流产。抗磷脂抗体和β 2 糖蛋白 1(β(2)GP1)自身抗体在 APS 的发病机制中起着重要作用。β(2)GP1 结构域 1(β(2)GP1-D1)的抗体已被认为是血栓形成的风险标志物,并且在一定程度上是 APS 患者妊娠并发症的风险标志物。尽管人们对抗-β(2)GP1-D1 抗体非常感兴趣,并且有相当多的研究历史,但研究数量仍然有限,并且对该生物标志物的临床意义的接受程度仍在不断发展。本综述总结了目前对抗-β(2)GP1-D1 抗体的认识,并提供了对最新发现的见解。此外,我们提出了一个未来研究的建议指南,以更好地理解和验证抗-β(2)GP1-D1 抗体的临床应用。