SARS-CoV-2 spike-specific nasal-resident CD49a+CD8+ memory T cells exert immediate effector functions with enhanced IFN-γ production

Nat Commun. 2024 Sep 27;15(1):8355. doi: 10.1038/s41467-024-52689-5.

Abstract

Virus-specific nasal resident T cells are important for protection against subsequent infection with a similar virus. Here we examine the phenotypes and functions of SARS-CoV-2-specific T cells in the nasal mucosa of vaccinated individuals with breakthrough infection (BTI) or without infection. Nasal tissues are obtained from participants during sinus surgery. Analysis of activation-induced markers implicates that a considerable proportion of spike (S)-reactive nasal CD8+ T cells express CD103, a tissue-resident marker. MHC-I multimer staining is performed to analyze the ex vivo phenotype and function of SARS-CoV-2 S-specific CD8+ T cells. We detect multimer+CD8+ T cells with tissue-resident phenotypes in nasal tissue samples from vaccinees without infection as well as vaccinees with BTI. Multimer+CD8+ T cells remain present in nasal tissues over one year after the last exposure to S antigen, although the frequency decreases. Upon direct ex vivo stimulation with epitope peptides, nasal multimer+CD8+ T cells-particularly the CD49a+ subset-exhibit immediate effector functions, including IFN-γ production. CITE-seq analysis of S-reactive AIM+CD8+ T cells confirms the enhanced effector function of the CD49a+ subset. These findings indicate that among individuals previously exposed to S antigen by vaccination or BTI, S-specific nasal-resident CD49a+CD8+ memory T cells can rapidly respond to SARS-CoV-2 during infection or reinfection.

MeSH terms

  • Adult
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • CD8-Positive T-Lymphocytes* / immunology
  • COVID-19 Vaccines / immunology
  • COVID-19* / immunology
  • COVID-19* / virology
  • Female
  • Humans
  • Immunologic Memory / immunology
  • Integrin alpha Chains
  • Integrin alpha1 / immunology
  • Integrin alpha1 / metabolism
  • Interferon-gamma* / immunology
  • Interferon-gamma* / metabolism
  • Male
  • Memory T Cells* / immunology
  • Middle Aged
  • Nasal Mucosa* / immunology
  • Nasal Mucosa* / virology
  • SARS-CoV-2* / immunology
  • Spike Glycoprotein, Coronavirus* / immunology

Substances

  • Spike Glycoprotein, Coronavirus
  • Interferon-gamma
  • spike protein, SARS-CoV-2
  • Integrin alpha1
  • COVID-19 Vaccines
  • Antigens, CD
  • alpha E integrins
  • Integrin alpha Chains