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

Research output: Contribution to journalArticlepeer-review

108 Scopus citations

Abstract

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.

Original languageEnglish
Article number102885
JournaleBioMedicine
Volume57
DOIs
StatePublished - Jul 2020
Externally publishedYes

Keywords

  • COVID-19
  • Flow cytometry
  • GLP
  • Outcome
  • SARS-CoV-2
  • Severity
  • Standardization
  • T cell memory
  • T cell response
  • T cells

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