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与新型冠状病毒肺炎相关的血栓形成和止血障碍:交叉反应性和免疫印记的可能因果作用。

Thromboses and Hemostasis Disorders Associated with COVID-19: The Possible Causal Role of Cross-Reactivity and Immunological Imprinting.

作者信息

Kanduc Darja

机构信息

Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.

出版信息

Glob Med Genet. 2021 Jun 26;8(4):162-170. doi: 10.1055/s-0041-1731068. eCollection 2021 Dec.

Abstract

By examining the issue of the thromboses and hemostasis disorders associated with severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) through the lens of cross-reactivity, it was found that 60 pentapeptides are shared by SARS-CoV-2 spike glycoprotein (gp) and human proteins that- when altered, mutated, deficient or, however, improperly functioning- cause vascular diseases, thromboembolic complications, venous thrombosis, thrombocytopenia, coagulopathies, and bleeding, inter alia. The peptide commonality has a relevant immunological potential as almost all of the shared sequences are present in experimentally validated SARS-CoV-2 spike gp-derived epitopes, thus supporting the possibility of cross-reactions between the viral gp and the thromboses-related human proteins. Moreover, many of the shared peptide sequences are also present in pathogens to which individuals have previously been exposed following natural infection or vaccinal routes, and of which the immune system has stored imprint. Such an immunological memory might rapidly trigger anamnestic secondary cross-reactive responses of extreme affinity and avidity, in this way explaining the thromboembolic adverse events that can associate with SARS-CoV-2 infection or active immunization.

摘要

通过交叉反应的视角研究与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)相关的血栓形成和止血障碍问题时发现,SARS-CoV-2刺突糖蛋白(gp)与人蛋白质共有60种五肽,这些人蛋白质在发生改变、突变、缺陷或功能异常时会导致血管疾病、血栓栓塞并发症、静脉血栓形成、血小板减少症、凝血病和出血等。这种肽的共性具有相关的免疫潜力,因为几乎所有共享序列都存在于经过实验验证的SARS-CoV-2刺突gp衍生表位中,从而支持了病毒gp与血栓形成相关的人类蛋白质之间发生交叉反应的可能性。此外,许多共享肽序列也存在于个体先前通过自然感染或疫苗接种途径接触过的病原体中,免疫系统已经对这些病原体有了记忆。这种免疫记忆可能会迅速触发具有极高亲和力和avidity的回忆性二次交叉反应,从而解释了与SARS-CoV-2感染或主动免疫相关的血栓栓塞不良事件。

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