CD5 Suppresses IL-15-Induced Proliferation of Human Memory CD8+ T Cells by Inhibiting mTOR Pathways

J Immunol. 2022 Sep 15;209(6):1108-1117. doi: 10.4049/jimmunol.2100854. Epub 2022 Aug 24.

Abstract

IL-15 induces the proliferation of memory CD8+ T cells as well as NK cells. The expression of CD5 inversely correlates with the IL-15 responsiveness of human memory CD8+ T cells. However, whether CD5 directly regulates IL-15-induced proliferation of human memory CD8+ T cells is unknown. In the current study, we demonstrate that human memory CD8+ T cells in advanced stages of differentiation respond to IL-15 better than human memory CD8+ T cells in stages of less differentiation. We also found that the expression level of CD5 is the best correlate for IL-15 hyporesponsiveness among human memory CD8+ T cells. Importantly, we found that IL-15-induced proliferation of human memory CD8+ T cells is significantly enhanced by blocking CD5 with Abs or knocking down CD5 expression using small interfering RNA, indicating that CD5 directly suppresses the IL-15-induced proliferation of human memory CD8+ T cells. We also found that CD5 inhibits activation of the mTOR pathway, which is required for IL-15-induced proliferation of human memory CD8+ T cells. Taken together, the results indicate that CD5 is not just a correlative marker for IL-15 hyporesponsiveness, but it also directly suppresses IL-15-induced proliferation of human memory CD8+ T cells by inhibiting mTOR pathways.

MeSH terms

  • CD5 Antigens* / metabolism
  • CD8-Positive T-Lymphocytes* / cytology
  • Cell Proliferation
  • Humans
  • Immunologic Memory
  • Interleukin-15* / immunology
  • Lymphocyte Activation
  • RNA, Small Interfering
  • TOR Serine-Threonine Kinases* / metabolism

Substances

  • CD5 Antigens
  • Interleukin-15
  • RNA, Small Interfering
  • MTOR protein, human
  • TOR Serine-Threonine Kinases