COVID-19和抗磷脂抗体

IF 2.2 4区 医学 Q3 HEMATOLOGY Best Practice & Research Clinical Haematology Pub Date : 2022-09-01 DOI:10.1016/j.beha.2022.101402
Ayesha Butt , Doruk Erkan , Alfred Ian Lee
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引用次数: 6

摘要

抗磷脂综合征和COVID-19的凝血功能障碍具有许多共同的病理生理特征,包括内皮病变、高凝性、血小板活化、补体途径和中性粒细胞细胞外陷阱,所有这些都通过免疫血栓形成模型协同作用。在COVID-19中产生抗磷脂抗体很常见,在一些研究中,50%的COVID-19患者狼疮抗凝血剂呈阳性,非札幌标准的抗磷脂抗体也很普遍。抗磷脂抗体在COVID-19中的生物学意义尚不确定,因为这种抗体通常是短暂的,并且对有无抗磷脂抗体的COVID-19患者临床结局的研究得出了相互矛盾的结果。在这篇综述中,我们探讨了抗磷脂抗体在COVID-19和其他感染中的生物学作用,并讨论了抗磷脂综合征的血栓形成机制以及与COVID-19凝血功能障碍的相似之处。此外,我们还回顾了现有关于抗磷脂抗体和抗磷脂综合征患者接种COVID-19疫苗安全性的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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COVID-19 and antiphospholipid antibodies

Antiphospholipid syndrome and the coagulopathy of COVID-19 share many pathophysiologic features, including endotheliopathy, hypercoagulability, and activation of platelets, complement pathways, and neutrophil extracellular traps, all acting in concert via a model of immunothrombosis. Antiphospholipid antibody production in COVID-19 is common, with 50% of COVID-19 patients being positive for lupus anticoagulant in some studies, and with non-Sapporo criteria antiphospholipid antibodies being prevalent as well. The biological significance of antiphospholipid antibodies in COVID-19 is uncertain, as such antibodies are usually transient, and studies examining clinical outcomes in COVID-19 patients with and without antiphospholipid antibodies have yielded conflicting results. In this review, we explore the biology of antiphospholipid antibodies in COVID-19 and other infections and discuss mechanisms of thrombogenesis in antiphospholipid syndrome and parallels with COVID-19 coagulopathy. In addition, we review the existing literature on safety of COVID-19 vaccination in patients with antiphospholipid antibodies and antiphospholipid syndrome.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
期刊最新文献
Erratum to “Special issue 37.2 and 37.3 Genetics and Function of HLA and immune-related genes in transplantation and cellular immunotherapy” [Best Pract Res Clin Haematol (2024) 101588] Editorial Board From clones to immunopeptidomes: New developments in the characterization of permissive HLA-DP mismatches in hematopoietic cell transplantation Relevance of donor-specific HLA antibodies in hematopoietic cell transplantation HLA structure and function in hematopoietic-cell transplantation
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