Frontiers in Immunology (Oct 2022)

Differential activation of human neutrophils by SARS-CoV-2 variants of concern

  • Samuel Lebourgeois,
  • Ambroise David,
  • Houssem Redha Chenane,
  • Vanessa Granger,
  • Vanessa Granger,
  • Reyene Menidjel,
  • Nadhira Fidouh,
  • Benoît Noël,
  • Olivier Delelis,
  • Clémence Richetta,
  • Charlotte Charpentier,
  • Charlotte Charpentier,
  • Sylvie Chollet-Martin,
  • Sylvie Chollet-Martin,
  • Diane Descamps,
  • Diane Descamps,
  • Benoit Visseaux,
  • Benoit Visseaux,
  • Luc de Chaisemartin,
  • Luc de Chaisemartin

DOI
https://doi.org/10.3389/fimmu.2022.1010140
Journal volume & issue
Vol. 13

Abstract

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The emerging SARS-CoV-2 virus has affected the entire world with over 600 million confirmed cases and 6.5 million deaths as of September 2022. Since the beginning of the pandemic, several variants of SARS-CoV-2 have emerged, with different infectivity and virulence. Several studies suggest an important role of neutrophils in SARS-Cov-2 infection severity, but data about direct activation of neutrophils by the virus is scarce. Here, we studied the in vitro activation of human neutrophils by SARS-CoV-2 variants of concern (VOCs). In our work, we show that upon stimulation with SARS-Cov-2 infectious particles, human healthy resting neutrophils upregulate activation markers, degranulate IL-8, produce Reactive Oxygen Species and release Neutrophil Extracellular Traps. Neutrophil activation was dependent on TLR7/8 and IRF3/STING. We then compared the activation potential of neutrophils by SARS-CoV-2 variants and showed a significantly increased activation by the Delta variant and a decreased activation by the Omicron variant as compared to the initial strain. In this study, we demonstrate that the SARS-Cov-2 virus can directly activate neutrophils in COVID-19 and that the different VOCs had differences in neutrophil activation intensity that mirror the differences of clinical severity. These data highlight the need to address neutrophil-virus interactions as a potential target for therapeutic intervention in SARS-CoV-2 infection.

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