Antiphospholipid syndrome in the era of COVID-19 – Two sides of a coin

抗磷脂综合征 细胞激素风暴 自身免疫 医学 免疫学 后遗症 2019年冠状病毒病(COVID-19) 狼疮抗凝剂 疾病 血栓形成 抗体 传染病(医学专业) 内科学 精神科
作者
Naim Mahroum,Mona Habra,Mohamad Aosama Alrifaai,Yehuda Shoenfeld
出处
期刊:Autoimmunity Reviews [Elsevier BV]
卷期号:23 (9): 103543-103543 被引量:2
标识
DOI:10.1016/j.autrev.2024.103543
摘要

In addition to the respiratory symptoms associated with COVID-19, the disease has consistently been linked to many autoimmune diseases such as systemic lupus erythematous and antiphospholipid syndrome (APS). APS in particular was of paramount significance due to its devastating clinical sequela. In fact, the hypercoagulable state seen in patients with acute COVID-19 and the critical role of anticoagulant treatment in affected individuals shed light on the possible relatedness between APS and COVID-19. Moreover, the role of autoimmunity in the assumed association is not less important especially with the accumulated data available regarding the autoimmunity-triggering effect of SARS-CoV-2 infection. This is furtherly strengthened at the time patients with COVID-19 manifested antiphospholipid antibodies of different types following infection. Additionally, the severe form of the APS spectrum, catastrophic APS (CAPS), was shown to have overlapping characteristics with severe COVID-19 such as cytokine storm and multi-organ failure. Interestingly, COVID vaccine-induced autoimmune phenomena described in the medical literature have pointed to an association with APS. Whether the antiphospholipid antibodies were present or de novo, COVID vaccine-induced vascular thrombosis in certain individuals necessitates further investigations regarding the possible mechanisms involved. In our current paper, we aimed to focus on the associations mentioned, their implications, importance, and consequences.
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