| Literature DB >> 33598783 |
Baofu Zhang1,2,3, Huizhong Li3, Wenbin Liu3, Hui Tian3, Liantao Li2,3, Chao Gao2,3, Junnian Zheng4,5,6.
Abstract
Adoptive transfer of γδ T cells is an attractive approach for cell-based immunotherapy in treatment of renal cell carcinoma (RCC). Interleukin-15 (IL-15) is the key physiological cytokine that regulates γδ T cell differentiation, proliferation and survival. In this work, we determined that IL-15 have the capacity to enhance the anti-tumoral functions of γδ T cells. IL-15 can induce the upregulation of cytotoxicity-associated molecules on the γδ T cell surface, incite γδ T cell proliferation and decrease apoptosis. Moreover, the enhanced cytotoxicity of IL-15-induced γδ T cell was dependent on the interaction of NKG2D and MICA. Most importantly, we found that IL-15-induced γδ T cells effectively suppressed the tumor growth in vivo and prolonged the survival time of RCC-bearing patient‑derived xenograft (PDX) mice. These results are important for the prospective use of γδ T cells in clinical practice when designing novel cell-based immunotherapies against RCC.Entities:
Keywords: IL-15; Immunotherapy; NKG2D; PDX; Renal cell carcinoma; γδ T cell
Year: 2021 PMID: 33598783 DOI: 10.1007/s12032-021-01474-1
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064