生物
效应器
背景(考古学)
CD8型
细胞毒性T细胞
免疫疗法
肿瘤微环境
免疫系统
过继性细胞移植
T细胞
过继免疫治疗
癌症免疫疗法
癌症研究
免疫学
体外
遗传学
古生物学
作者
Michael St. Paul,Pamela S. Ohashi
标识
DOI:10.1016/j.tcb.2020.06.003
摘要
There are multiple subsets of CD8+ T cells, not all of which have cytotoxic function and produce IFN-γ. A variety of Tc subsets have been detected within the TME and, depending on the subset, can be either positively or negatively correlated with prognosis. In the context of adoptive immunotherapy to treat cancer, the degree of tumor control is greatly influenced by the subset of T cells transferred. Effector CD8+ T cells are typically thought to be a homogenous group of cytotoxic cells that produce interferon-(IFN) γ. However, recent findings have challenged this notion because multiple subsets of CD8+ T cells have been described, each with distinct effector functions and cytotoxic potential. These subsets, referred to as the Tc subsets, have also been detected in tumor microenvironments (TMEs), where they potentially influence the antitumor response and patient outcomes. In this review, we highlight the prevalence and roles of Tc subsets in the TME. We also discuss their therapeutic applications in the context of adoptive immunotherapy to treat cancer. Effector CD8+ T cells are typically thought to be a homogenous group of cytotoxic cells that produce interferon-(IFN) γ. However, recent findings have challenged this notion because multiple subsets of CD8+ T cells have been described, each with distinct effector functions and cytotoxic potential. These subsets, referred to as the Tc subsets, have also been detected in tumor microenvironments (TMEs), where they potentially influence the antitumor response and patient outcomes. In this review, we highlight the prevalence and roles of Tc subsets in the TME. We also discuss their therapeutic applications in the context of adoptive immunotherapy to treat cancer.
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