EBioMedicine (Jul 2020)

Reappearance of effector T cells is associated with recovery from COVID-19

  • Ivan Odak,
  • Joana Barros-Martins,
  • Berislav Bošnjak,
  • Klaus Stahl,
  • Sascha David,
  • Olaf Wiesner,
  • Markus Busch,
  • Marius M. Hoeper,
  • Isabell Pink,
  • Tobias Welte,
  • Markus Cornberg,
  • Matthias Stoll,
  • Lilia Goudeva,
  • Rainer Blasczyk,
  • Arnold Ganser,
  • Immo Prinz,
  • Reinhold Förster,
  • Christian Koenecke,
  • Christian R. Schultze-Florey

Journal volume & issue
Vol. 57
p. 102885

Abstract

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Background: Elucidating the role of T cell responses in COVID-19 is of utmost importance to understand the clearance of SARS-CoV-2 infection. Methods: 30 hospitalized COVID-19 patients and 60 age- and gender-matched healthy controls (HC) participated in this study. We used two comprehensive 11-colour flow cytometric panels conforming to Good Laboratory Practice and approved for clinical diagnostics. Findings: Absolute numbers of lymphocyte subsets were differentially decreased in COVID-19 patients according to clinical severity. In severe disease (SD) patients, all lymphocyte subsets were reduced, whilst in mild disease (MD) NK, NKT and γδ T cells were at the level of HC. Additionally, we provide evidence of T cell activation in MD but not SD, when compared to HC. Follow up samples revealed a marked increase in effector T cells and memory subsets in convalescing but not in non-convalescing patients. Interpretation: Our data suggest that activation and expansion of innate and adaptive lymphocytes play a major role in COVID-19. Additionally, recovery is associated with formation of T cell memory as suggested by the missing formation of effector and central memory T cells in SD but not in MD. Understanding T cell-responses in the context of clinical severity might serve as foundation to overcome the lack of effective anti-viral immune response in severely affected COVID-19 patients and can offer prognostic value as biomarker for disease outcome and control. Funding: Funded by State of Lower Saxony grant 14–76,103–184CORONA-11/20 and German Research Foundation, Excellence Strategy – EXC2155“RESIST”–Project ID39087428, and DFG-SFB900/3–Project ID158989968, grants SFB900-B3, SFB900-B8.

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