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疫苗诱导的免疫性血栓性血小板减少症:我们目前了解多少?

Vaccine-induced immune thrombotic thrombocytopenia: what do we know hitherto?

作者信息

Roytenberg Renat, García-Sastre Adolfo, Li Wei

机构信息

Department of Biomedical Sciences, Joan C. Edwards School of Medicine at Marshall University, Huntington, WV, United States.

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

出版信息

Front Med (Lausanne). 2023 May 16;10:1155727. doi: 10.3389/fmed.2023.1155727. eCollection 2023.

Abstract

Vaccine-induced immune thrombotic thrombocytopenia (VITT), also known as thrombosis with thrombocytopenia syndrome, is a catastrophic and life-threatening reaction to coronavirus disease 2019 (COVID-19) vaccines, which occurs disproportionately in response to vaccination with non-replicating adenovirus vector (AV) vaccines. The mechanism of VITT is not well defined and it has not been resolved why cases of VITT are predominated by vaccination with AV vaccines. However, virtually all VITT patients have positive platelet-activating anti-platelet factor 4 (PF4) antibody titers. Subsequently, platelets are activated and depleted in an Fcγ-receptor IIa (FcγRIIa or CD32a)-dependent manner, but it is not clear why or how the anti-PF4 response is mounted. This review describes the pathogenesis of VITT and provides insight into possible mechanisms that prompt the formation of a PF4/polyanion complex, which drives VITT pathology, as an amalgam of current experimental data or hypotheses.

摘要

疫苗诱导的免疫性血栓性血小板减少症(VITT),也称为伴有血小板减少症的血栓形成综合征,是一种针对2019冠状病毒病(COVID-19)疫苗的灾难性且危及生命的反应,在接种非复制型腺病毒载体(AV)疫苗后发生的比例过高。VITT的机制尚未明确,且为何VITT病例以接种AV疫苗为主也未得到解决。然而,几乎所有VITT患者的血小板活化抗血小板因子4(PF4)抗体滴度均为阳性。随后,血小板以Fcγ受体IIa(FcγRIIa或CD32a)依赖性方式被激活并消耗,但尚不清楚抗PF4反应为何发生或如何发生。本综述描述了VITT的发病机制,并根据当前的实验数据或假设,深入探讨了促使PF4/聚阴离子复合物形成从而驱动VITT病理过程的可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce46/10227460/a08372ec59fc/fmed-10-1155727-g001.jpg

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