Antiphospholipid综合症。

J. Manson, D. Isenberg
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引用次数: 1

摘要

抗磷脂综合征(APS)被定义为存在静脉或动脉血栓形成,和/或复发性流产,有抗磷脂抗体(aPL)的证据。这种疾病的核心是产生针对磷脂分子本身或其结合蛋白的抗体。这些抗体的产生可能取决于细胞凋亡过程中细胞质分子的异常暴露。抗磷脂综合征的确切发病机制尚不清楚,但存在各种假定的模型。这些包括内皮细胞粘附分子的上调,脂质过氧化过程中的膜破坏,内源性抗凝血剂的功能障碍或血小板聚集异常。主要的治疗方法是阿司匹林或华法林,需要更多的研究来发现新的、更安全的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiphospholipid syndrome.
Antiphospholipid syndrome (APS) is defined as the presence of venous or arterial thromboses, and/or recurrent miscarriage, with evidence of antiphospholipid antibodies (aPL). Central to the disease, is the development of the antibodies to phospholipid molecules themselves, or to their binding proteins. The production of these antibodies may depend upon the unusual exposure of cytoplasmic molecules seen during the process of apoptosis. The exact pathogenesis of antiphospholipid syndrome remains unclear, but various putative models exist. These include the up-regulation of endothelial cell adhesion molecules, membrane disruption during lipid peroxidation, a dysfunction of endogenous anticoagulants, or abnormal platelet aggregation. The mainstay of treatment is with aspirin or warfarin, and more research is required to discover novel, and safer, therapies.
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