Contribution of the von Willebrand factor/ADAMTS13 imbalance to COVID-19 coagulopathy

被引:18
|
作者
Seth, Ryan [1 ]
McKinnon, Thomas A. J. [2 ]
Zhang, X. Frank [1 ]
机构
[1] Lehigh Univ, Dept Bioengn, Bethlehem, PA 18015 USA
[2] Imperial Coll London, Ctr Haematol, Dept Immunol & Inflammat, London, England
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
coagulopathy; COVID-19; endothelium; thrombosis; von Willebrand factor; ADAMTS13; ACTIVITY; ISCHEMIC-STROKE; FACTOR-VIII; THROMBOSIS; SAFETY; RISK; PHARMACOKINETICS; COMPLICATIONS; INFLAMMATION; FIBRINOGEN;
D O I
10.1152/ajpheart.00204.2021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The 2019 coronavirus disease (COVID-19) is the disease caused by SARS-CoV-2 infection. Although this infection has been shown to affect the respiratory system, a high incidence of thrombotic events has been observed in severe cases of COVID19 and in a significant portion of COVID-19 nonsurvivors. Although prior literature has reported on both the coagulopathy and hypercoagulability of COVID-19, the specifics of coagulation have not been fully investigated. Observations of microthrombosis in patients with COVID-19 have brought attention to potential inflammatory endothelial injury. Von Willebrand factor (VWF) and its protease, A disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13), play an important homeostatic role in responding to endothelial injury. This report provides an overview of the literature investigating the role the VWF/ADAMTS13 axis may have in COVID-19 thrombotic events and suggests potential therapeutic strategies to prevent the progression of coagulopathy in patients with COVID-19.
引用
收藏
页码:H87 / H93
页数:7
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