Cell Reports Medicine (Sep 2020)

SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential

  • Jason Neidleman,
  • Xiaoyu Luo,
  • Julie Frouard,
  • Guorui Xie,
  • Gurjot Gill,
  • Ellen S. Stein,
  • Matthew McGregor,
  • Tongcui Ma,
  • Ashley F. George,
  • Astrid Kosters,
  • Warner C. Greene,
  • Joshua Vasquez,
  • Eliver Ghosn,
  • Sulggi Lee,
  • Nadia R. Roan

Journal volume & issue
Vol. 1, no. 6
p. 100081

Abstract

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Summary: Convalescing coronavirus disease 2019 (COVID-19) patients mount robust T cell responses against SARS-CoV-2, suggesting an important role of T cells in viral clearance. To date, the phenotypes of SARS-CoV-2-specific T cells remain poorly defined. Using 38-parameter CyTOF, we phenotyped longitudinal specimens of SARS-CoV-2-specific CD4+ and CD8+ T cells from nine individuals who recovered from mild COVID-19. SARS-CoV-2-specific CD4+ T cells were exclusively Th1 cells and predominantly Tcm cells with phenotypic features of robust helper function. SARS-CoV-2-specific CD8+ T cells were predominantly Temra cells in a state of less terminal differentiation than most Temra cells. Subsets of SARS-CoV-2-specific T cells express CD127, can proliferate homeostatically, and can persist for over 2 months. Our results suggest that long-lived and robust T cell immunity is generated following natural SARS-CoV-2 infection and support an important role of SARS-CoV-2-specific T cells in host control of COVID-19.

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