Fibrinogen, Fibrin, and Fibrin Degradation Products in COVID-19

被引:31
作者
Kangro, Kadri [1 ]
Wolberg, Alisa S. S. [1 ]
Flick, Matthew J. [1 ,2 ,3 ]
机构
[1] Univ North Carolina Chapel Hill, UNC Blood Res Ctr, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[2] Univ North Carolina Chapel Hill, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[3] Univ North Carolina Chapel Hill, UNC Blood Res Ctr, Chapel Hill, NC 27599 USA
关键词
Fibrinogen; fibrin; D-dimer; coagulation; fibrinolysis; COVID-19; CORONAVIRUS DISEASE 2019; BLOOD-CELL RETENTION; VENOUS THROMBOEMBOLISM; FACTOR-XIII; D-DIMER; COAGULATION; BINDING; ACTIVATION; THROMBOSIS; ENGAGEMENT;
D O I
10.2174/1389450123666220826162900
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is the highly pathogenicand highly transmissible human coronavirus that is the causative agent for the worldwideCOVID-19 pandemic. COVID-19 manifests predominantly as a respiratory illness with symptomsconsistent with viral pneumonia, but other organ systems (e.g., kidney, heart, brain) can also becomeperturbed in COVID-19 patients. Accumulating data suggest that significant activation of thehemostatic system is a common pathological manifestation of SARS-CoV-2 infection. The clottingprotein fibrinogen is one of the most abundant plasma proteins. Following activation of coagulation,the central coagulation protease thrombin converts fibrinogen to fibrin monomers, which selfassembleto form a matrix, the primary structural component of the blood clot. Severe COVID-19 isassociated with a profound perturbation of circulating fibrinogen, intra- and extravascular fibrindeposition and persistence, and fibrin degradation. Current findings suggest high levels of fibrinogenand the fibrin degradation product D-dimer are biomarkers of poor prognosis in COVID-19.Moreover, emerging studies with in vitro and animal models indicate fibrin(ogen) as an active playerin COVID-19 pathogenesis. Here, we review the current literature regarding fibrin(ogen) andCOVID-19, including possible pathogenic mechanisms and treatment strategies centered on clottingand fibrin(ogen) function.
引用
收藏
页码:1593 / 1602
页数:10
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