CD4 and IL-2 mediated NK cell responses after COVID-19 infection and mRNA vaccination in adults

Immunobiology. 2023 Jan;228(1):152304. doi: 10.1016/j.imbio.2022.152304. Epub 2022 Nov 23.

Abstract

A detailed understanding of protective immunity against SARS-CoV-2 is incredibly important in fighting the pandemic. Central to protective immunity is the ability of the immune system to recall previous exposures. Although antibody and T cell immunity have gained considerable attention, the contribution of the NK cell compartment to immune recall and protection from SARS-CoV-2 has not been explored. In this study, we investigate the NK cell responses to stimulation with SARS-CoV-2 in previously exposed and non-exposed individuals. We show that NK cells demonstrate an enhanced CD4+ T cell dependent response when re-exposed to SARS-CoV-2 antigen. The enhanced response is dependent on T cells and correlates with the number of SARS-CoV-2 specific CD4 T cells. We find that IL-2 is a critical mediator of NK cell function. These findings suggest that NK cells contribute to the protective responses against SARS-CoV-2 through a cooperation with antigen-specific CD4 T cells and have significant implications on our understanding of protective immunity in SARS-CoV-2.

Keywords: Adaptive immunity; BNT162b2; CD4; COVID-19; IL-2; Memory; NK cells.

MeSH terms

  • Adult
  • Antibodies, Viral / immunology
  • CD4-Positive T-Lymphocytes
  • COVID-19* / immunology
  • COVID-19* / prevention & control
  • Humans
  • Interleukin-2*
  • Killer Cells, Natural* / immunology
  • SARS-CoV-2
  • Vaccination
  • mRNA Vaccines* / immunology

Substances

  • Antibodies, Viral
  • Interleukin-2
  • mRNA Vaccines