Collaboration between IL-7 and IL-15 enables adaptation of tissue-resident and circulating memory CD8⁺ T cells.

ABSTRACT: Interleukin-7 (IL-7) is considered a critical regulator of memory CD8⁺ T cell homeostasis, but this is primarily based on analysis of circulating and not tissue-resident memory (T_RM) subsets. Furthermore, the cell-intrinsic requirement for IL-7 signaling during memory homeostasis has not been directly tested. Using inducible deletion, we found that Il7ra loss had only a modest effect on persistence of circulating memory and T_RM subsets and that IL-7Rα was primarily required for normal basal proliferation. Loss of IL-15 signaling imposed heightened IL-7Rα dependence on memory CD8⁺ T cells, including T_RM populations previously described as IL-15-independent. In the absence of IL-15 signaling, IL-7Rα was upregulated, and loss of IL

SUBMITTER: Jarjour NN 

PROVIDER: S-EPMC11185530 | biostudies-literature | 2024 Jun

REPOSITORIES: biostudies-literature