Thromboinflammation supports complement activation in cancer patients with COVID-19 Journal Article


Authors: Peerschke, E. I.; Valentino, A.; So, R. J.; Shulman, S.; Ravinder
Article Title: Thromboinflammation supports complement activation in cancer patients with COVID-19
Abstract: Background: COVID-19 pathology is associated with exuberant inflammation, vascular damage, and activation of coagulation. In addition, complement activation has been described and is linked to disease pathology. However, few studies have been conducted in cancer patients. Objective: This study examined complement activation in response to COVID-19 in the setting of cancer associated thromboinflammation. Methods: Markers of complement activation (C3a, C5a, sC5b-9) and complement inhibitors (Factor H, C1-Inhibitor) were evaluated in plasma of cancer patients with (n=43) and without (n=43) COVID-19 and stratified based on elevated plasma D-dimer levels (>1.0 μg/ml FEU). Markers of vascular endothelial cell dysfunction and platelet activation (ICAM-1, thrombomodulin, P-selectin) as well as systemic inflammation (pentraxin-3, serum amyloid A, soluble urokinase plasminogen activator receptor) were analyzed to further evaluate the inflammatory response. Results: Increases in circulating markers of endothelial cell dysfunction, platelet activation, and systemic inflammation were noted in cancer patients with COVID-19. In contrast, complement activation increased in cancer patients with COVID-19 and elevated D-dimers. This was accompanied by decreased C1-Inhibitor levels in patients with D-dimers > 5 ug/ml FEU. Conclusion: Complement activation in cancer patients with COVID-19 is significantly increased in the setting of thromboinflammation. These findings support a link between coagulation and complement cascades in the setting of inflammation. © Copyright © 2021 Peerschke, Valentino, So, Shulman and Ravinder.
Keywords: endothelial dysfunction; complement; cancer; covid-19; thromboinflammation
Journal Title: Frontiers in Immunology
Volume: 12
ISSN: 1664-3224
Publisher: Frontiers Media S.A.  
Date Published: 2021-08-18
Start Page: 716361
Language: English
DOI: 10.3389/fimmu.2021.716361
PROVIDER: scopus
PMCID: PMC8416543
PUBMED: 34491250
DOI/URL:
Notes: Article -- Export Date: 1 October 2021 -- Source: Scopus
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