%0 Journal Article
%A Madi, Alaa Abdelghani Mohamed
%A Wu, Jingxia
%A Ma, Sicong
%A Weisshaar, Nina
%A Mieg, Alessa
%A Hering, Marvin
%A Ming, Yanan
%A Zettl, Ferdinand
%A Mohr, Kerstin
%A Ten Bosch, Nora
%A Schlimbach, Tilo
%A Hertel, Franziska
%A Cui, Guoliang
%T Regulatory T cell-derived interleukin-15 promotes the diversity of immunological memory.
%J European journal of immunology
%V 53
%N 1
%@ 0014-2980
%C Weinheim
%I Wiley-VCH
%M DKFZ-2022-02486
%P e2149400
%D 2023
%Z #EA:D192#LA:D192# / 2023 Jan;53(1):e2149400 / HI-TRON
%X While the immunosuppressive function of regulatory T (Treg) cells has been extensively studied, their immune-supportive roles have been less well investigated. Using a lymphocytic choriomeningitis virus (LCMV) Armstrong infection mouse model, we found that Treg cell-derived interleukin (IL)-15 is required for long-term maintenance of the KLRG1+ IL-7Rα- CD62L- terminal effector memory CD8+ T (tTEM) cell subset, but dispensable for the suppressive function of Treg cells themselves. In contrast, deletion of Il15 from other sources, including myeloid cells and muscles, did not affect the composition of the memory CD8+ T cell pool. Our findings identify Treg cells as an essential IL-15 source maintaining tTEM cells and suggest that Treg cells promote the diversity of immunological memory. This article is protected by copyright. All rights reserved.
%K IL-15 ⋅ Treg cells ⋅ Effector memory ⋅ T cells (Other)
%F PUB:(DE-HGF)16
%9 Journal Article
%$ pmid:36263815
%R 10.1002/eji.202149400
%U https://inrepo02.dkfz.de/record/182184