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 (Shared last author)
  • Christian R Schultze-Florey (Shared last author)

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.

Bibliographical data

Original languageEnglish
Article number102885
ISSN2352-3964
DOIs
Publication statusPublished - 07.2020
Externally publishedYes
PubMed 32650275