Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation

Elife. 2021 Mar 23:10:e64909. doi: 10.7554/eLife.64909.

Abstract

Numerous reports of vascular events after an initial recovery from COVID-19 form our impetus to investigate the impact of COVID-19 on vascular health of recovered patients. We found elevated levels of circulating endothelial cells (CECs), a biomarker of vascular injury, in COVID-19 convalescents compared to healthy controls. In particular, those with pre-existing conditions (e.g., hypertension, diabetes) had more pronounced endothelial activation hallmarks than non-COVID-19 patients with matched cardiovascular risk. Several proinflammatory and activated T lymphocyte-associated cytokines sustained from acute infection to recovery phase, which correlated positively with CEC measures, implicating cytokine-driven endothelial dysfunction. Notably, we found higher frequency of effector T cells in our COVID-19 convalescents compared to healthy controls. The activation markers detected on CECs mapped to counter receptors found primarily on cytotoxic CD8+ T cells, raising the possibility of cytotoxic effector cells targeting activated endothelial cells. Clinical trials in preventive therapy for post-COVID-19 vascular complications may be needed.

Keywords: COVID-19; cell biology; circulating endothelial cells; cytokines; endothelial activation; human; immune effector cells; immunology; inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • COVID-19 / complications*
  • COVID-19 / immunology
  • COVID-19 / pathology
  • Cardiovascular Diseases / etiology*
  • Cardiovascular Diseases / immunology
  • Cardiovascular Diseases / pathology
  • Cytokines / immunology
  • Endothelial Cells / immunology
  • Endothelial Cells / pathology
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / pathology*
  • Female
  • Humans
  • Lymphocyte Activation*
  • Male
  • Middle Aged
  • Risk Factors

Substances

  • Cytokines

Associated data

  • GEO/GSE150728