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

Authors
Choi, YJ  | Lee, H | Kim, JH | Kim, SY | Koh, JY | Sa, M | Park, SH | Shin, EC
Citation
Journal of immunology (Baltimore, Md. : 1950), 209(6). : 1108-1117, 2022
Journal Title
Journal of immunology (Baltimore, Md. : 1950)
ISSN
0022-17671550-6606
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

DOI
10.4049/jimmunol.2100854
PMID
36002232
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Ophthalmology
Ajou Authors
최, 영준
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