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Review
. 2021 Aug;194(3):518-529.
doi: 10.1111/bjh.17664. Epub 2021 Jul 7.

COVID-19 and immunothrombosis: emerging understanding and clinical management

Affiliations
Review

COVID-19 and immunothrombosis: emerging understanding and clinical management

Rebecca J Shaw et al. Br J Haematol. 2021 Aug.

Abstract

The COVID-19 pandemic has been the most significant health crisis in recent global history. Early studies from Wuhan highlighted COVID-19-associated coagulopathy and a significant association with mortality was soon recognised. As research continues across the world, more evidence is emerging of the cross-talk between the innate immune system, coagulation activation and inflammation. Immunothrombosis has been demonstrated to play a key role in the pathophysiology of severe COVID-19, with extracellular histones and neutrophil extracellular traps detected in the plasma and cardiopulmonary tissues of critically ill patients. Targeting the components of immunothrombosis is becoming an important factor in the treatment of patients with COVID-19 infection. Recent studies report outcomes of intermediate and therapeutic anticoagulation in hospitalised patients with varying severities of COVID-19 disease, including optimal dosing and associated bleeding risks. Immunomodulatory therapies, including corticosteroids and IL-6 receptor antagonists, have been demonstrated to significantly reduce mortality in COVID-19 patients. As the pandemic continues, more studies are required to understand the driving factors and upstream mechanisms for coagulopathy and immunothrombosis in COVID-19, and thus potentially develop more targeted therapies for SARS-CoV-2 infection, both in the acute phase and in those who develop longer-term symptom burden.

Keywords: COVID-19; anticoagulation; coagulopathy; immunomodulatory; immunothrombosis.

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Comment in

  • Immunothrombosis: a COVID-19 concerto.
    Goshua G, Butt A, Lee AI. Goshua G, et al. Br J Haematol. 2021 Aug;194(3):491-493. doi: 10.1111/bjh.17666. Epub 2021 Jul 7. Br J Haematol. 2021. PMID: 34114208 No abstract available.

References

    1. WHO Coronavirus Disease (COVID-19) Dashboard. 2021. [Homepage on the internet]. [cited 29 April 2021). Available from: https://covid19.who.int/.
    1. Wu Z, McGoogan JM. Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72 314 cases from the Chinese Center for Disease Control and Prevention. JAMA. 2020;323(13):1239.
    1. Engelmann B, Massberg S. Thrombosis as an intravascular effector of innate immunity. Nat Rev Immunol. 2013;13(1):34-45.
    1. Bonaventura A, Vecchié A, Dagna L, Martinod K, Dixon DL, Van Tassell BW, et al. Endothelial dysfunction and immunothrombosis as key pathogenic mechanisms in COVID-19. Nat Rev Immunol. 2021;21(5):319-29.
    1. Ziegler CGK, Allon SJ, Nyquist SK, Mbano IM, Miao VN, Tzouanas CN, et al. SARS-CoV-2 Receptor ACE2 is an interferon-stimulated gene in human airway epithelial cells and is detected in specific cell subsets across tissues. Cell. 2020;181(5):1016-35.e19.