COVID-19: Complement, Coagulation, and Collateral Damage

J Immunol. 2020 Sep 15;205(6):1488-1495. doi: 10.4049/jimmunol.2000644. Epub 2020 Jul 22.

Abstract

Coronavirus disease of 2019 (COVID-19) is a highly contagious respiratory infection that is caused by the severe acute respiratory syndrome coronavirus 2. Although most people are immunocompetent to the virus, a small group fail to mount an effective antiviral response and develop chronic infections that trigger hyperinflammation. This results in major complications, including acute respiratory distress syndrome, disseminated intravascular coagulation, and multiorgan failure, which all carry poor prognoses. Emerging evidence suggests that the complement system plays a key role in this inflammatory reaction. Indeed, patients with severe COVID-19 show prominent complement activation in their lung, skin, and sera, and those individuals who were treated with complement inhibitors all recovered with no adverse reactions. These and other studies hint at complement's therapeutic potential in these sequalae, and thus, to support drug development, in this review, we provide a summary of COVID-19 and review complement's role in COVID-19 acute respiratory distress syndrome and coagulopathy.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Betacoronavirus / immunology
  • Blood Coagulation / drug effects
  • Blood Coagulation Disorders / immunology
  • Blood Coagulation Disorders / virology*
  • COVID-19
  • Complement Activation / drug effects
  • Complement Activation / physiology*
  • Complement Inactivating Agents / therapeutic use
  • Complement System Proteins / drug effects
  • Coronavirus Infections / blood
  • Coronavirus Infections / complications*
  • Coronavirus Infections / immunology
  • Humans
  • Inflammation / immunology
  • Inflammation / virology
  • Pandemics
  • Pneumonia, Viral / blood
  • Pneumonia, Viral / complications*
  • Pneumonia, Viral / immunology
  • Respiratory Distress Syndrome / virology*
  • SARS-CoV-2

Substances

  • Complement Inactivating Agents
  • Complement System Proteins