RORγt+ c-Maf+ Vγ4+ γδ T cells are generated in the adult thymus but do not reach the periphery

  • Tao Yang
  • Joana Barros-Martins
  • Ziqing Wang
  • Melanie Wencker
  • Jiang Zhang
  • Justine Smout
  • Prerna Gambhir
  • Anika Janssen
  • Anja Schimrock
  • Hristo Georgiev
  • Ximena León-Lara
  • Siegfried Weiss
  • Jochen Huehn
  • Immo Prinz
  • Andreas Krueger
  • Reinhold Foerster
  • Thierry Walzer
  • Sarina Ravens

Related Research units

Abstract

T cell receptor (TCR) Vγ4-expressing γδ T cells comprise interferon γ (IFNγ)- and interleukin-17 (IL-17)-producing effector subsets, with a preference for IL-17 effector fate decisions during early ontogeny. The existence of adult-thymus-derived IL-17+ T cells (γδ17) remains controversial. Here, we use a mouse model in which T cells are generated exclusively in the adult thymus and employ single-cell chromatin state analysis to study their development. We identify adult-thymus-derived Vγ4 T cells that have all the molecular programs to become IL-17 producers. However, they have reduced IL-17 production capabilities and rarely reach the periphery. Moreover, this study provides high-resolution profiles of Vγ4 T cells in the adult thymus and lymph nodes and identifies Zeb1 as a potential γδ17 cell regulator. Together, this study provides valuable insights into the developmental traits of Vγ4 T cells during adulthood and supports the idea of age-specific signals required for thymic export and/or peripheral maturation of γδ17 cells.

Bibliographical data

Original languageEnglish
ISSN2211-1247
DOIs
Publication statusPublished - 31.10.2023

Comment Deanary

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

PubMed 37815917