Emergence of dysfunctional neutrophils with a defect in arginase-1 release in severe COVID-19

JCI Insight. 2024 Sep 10;9(17):e171659. doi: 10.1172/jci.insight.171659.

Abstract

Neutrophilia occurs in patients infected with SARS-CoV-2 (COVID-19) and is predictive of poor outcomes. Here, we link heterogenous neutrophil populations to disease severity in COVID-19. We identified neutrophils with features of cellular aging and immunosuppressive capacity in mild COVID-19 and features of neutrophil immaturity and activation in severe disease. The low-density neutrophil (LDN) number in circulating blood correlated with COVID-19 severity. Many of the divergent neutrophil phenotypes in COVID-19 were overrepresented in the LDN fraction and were less detectable in normal-density neutrophils. Functionally, neutrophils from patients with severe COVID-19 displayed defects in neutrophil extracellular trap formation and reactive oxygen species production. Soluble factors secreted by neutrophils from these patients inhibited T cell proliferation. Neutrophils from patients with severe COVID-19 had increased expression of arginase-1 protein, a feature that was retained in convalescent patients. Despite this increase in intracellular expression, there was a reduction in arginase-1 release by neutrophils into serum and culture supernatants. Furthermore, neutrophil-mediated T cell suppression was independent of arginase-1. Our results indicate the presence of dysfunctional, activated, and immature neutrophils in severe COVID-19.

Keywords: COVID-19; Immunology; Neutrophils.

MeSH terms

  • Adult
  • Aged
  • Arginase* / metabolism
  • COVID-19* / blood
  • COVID-19* / immunology
  • Extracellular Traps / immunology
  • Extracellular Traps / metabolism
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neutrophil Activation
  • Neutrophils* / immunology
  • Neutrophils* / metabolism
  • Reactive Oxygen Species / metabolism
  • SARS-CoV-2* / immunology
  • Severity of Illness Index*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism

Substances

  • Arginase
  • ARG1 protein, human
  • Reactive Oxygen Species