抗磷脂抗体与APS肾病

R. Willis, E. González
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引用次数: 0

摘要

致病性抗磷脂抗体(aPL)的存在是抗磷脂综合征(APS)的特征,通过其对各种抗原靶点的作用介导了该疾病典型的复发性妊娠丢失和血栓形成。APS肾病是APS患者肾脏受累的特征性临床病理表现,是肾内血管闭塞性疾病的结果。APS肾病的典型临床特征和形态学病变已经被很好地描述,一些研究已经建立了这些特征与各种aPL存在之间的联系。在这篇综述中,我们概述了aPL介导的血栓形成的病理生理机制,APS肾病的临床和形态学特征,以及aPL作用与APS肾病发生的证据。
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Antiphospholipid antibodies and APS nephropathy
The presence of pathogenic antiphospholipid antibodies (aPL) is the characterizing feature of the antiphospholipid syndrome (APS), mediating the recurrent pregnancy loss and thrombosis typical of the disease through its action on various antigenic targets. APS nephropathy is the characteristic clinico-pathological manifestation of renal involvement in APS and occurs as a result of vaso-occlusive disease in the intrarenal vasculature. The typical clinical features and morphological lesions of APS nephropathy have been well characterized and several studies have established a link between these features and the presence of various aPL. In this review, we outline the proposed pathophysiological mechanisms of aPL-mediated thrombosis, the characteristic clinical and morphological features of APS nephropathy and the evidence linking aPL action to the occurrence of APS nephropathy.
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7
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