Cell Reports (Oct 2023)

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

Journal volume & issue
Vol. 42, no. 10
p. 113230

Abstract

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Summary: 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.

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