脂质结合型抗磷脂抗体:抗磷脂综合征的病理生理学和诊断意义。

IF 6.6 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Nadine Müller-Calleja, Wolfram Ruf, Karl J Lackner
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引用次数: 0

摘要

抗磷脂综合征(APS)是一种以存在致病性抗磷脂抗体(aPL)为特征的自身免疫性疾病。大约 30 年前,尽管抗心磷脂是 APS 的诊断标准之一,但不需要蛋白质辅助因子的脂质结合型 aPL 一直被认为与 APS 的发病机制无关。在本综述中,我们将总结来自体外研究、动物模型和流行病学研究的现有证据,这些证据表明这一观点已不再站得住脚。因此,我们将只简要介绍其他 aPL 在 APS 中的作用。这一主题已在其他地方进行了详细论述。我们将讨论实验室诊断的后果,以及为解决与不同 aPL 特异性的致病作用有关的未决问题而需要进行的未来研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lipid-binding antiphospholipid antibodies: significance for pathophysiology and diagnosis of the antiphospholipid syndrome.

The antiphospholipid syndrome (APS) is an autoimmune disease characterized by the presence of pathogenic antiphospholipid antibodies (aPL). Since approximately 30 years ago, lipid-binding aPL, which do not require a protein cofactor, have been regarded as irrelevant for APS pathogenesis even though anticardiolipin are a diagnostic criterion of APS. In this review, we will summarize the available evidence from in vitro studies, animal models, and epidemiologic studies, which suggest that this concept is no longer tenable. Accordingly, we will only briefly touch on the role of other aPL in APS. This topic has been amply reviewed in detail elsewhere. We will discuss the consequences for laboratory diagnostics and future research required to resolve open questions related to the pathogenic role of different aPL specificities.

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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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