脂质代谢
CD8型
肿瘤微环境
免疫疗法
免疫系统
T细胞
生物
癌症免疫疗法
细胞毒性T细胞
癌症研究
免疫学
生物化学
体外
标识
DOI:10.3389/fimmu.2022.1020422
摘要
Lipids and lipid metabolism play crucial roles in regulating T cell function and are tightly related to the establishment of immune memory. It is reported that tumor-infiltrating CD8 + T lymphocytes (CD8 + TILs) burn fats to restore their impaired effector function due to the lack of glucose. Conversely, fatty acids (FAs) and cholesterol in the tumor microenvironment (TME) drive the CD8 + TILs dysfunction. The origin of dysfunctional CD8 + TILs shares important features with memory T cell’s precursor, but whether lipids and/or lipid metabolism reprogramming directly influence the memory plasticity of dysfunctional CD8 + TILs remains elusive. It is necessary to understand the interplay between cellular lipid metabolism and dysfunction of CD8 + TILs in the case of targeting T cell’s metabolism to synergize cancer immunotherapy. Therefore, in this review, we summarize the latest research on CD8 + TILs lipid metabolism, evaluate the impacts of lipids in the TME to CD8 + TILs, and highlight the significance of promoting memory phenotype cell formation by targeting CD8 + T cells lipid metabolism to provide longer duration of cancer immunotherapy efficacy.
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