Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
College of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Sci Immunol. 2023 Sep;8(87):eadg3868. doi: 10.1126/sciimmunol.adg3868. Epub 2023 Sep 1.
Thirty years of foundational research investigating molecular and cellular mechanisms promoting T cell exhaustion are now enabling rational design of T cell-based therapies for the treatment of chronic infections and cancer. Once described as a static cell fate, it is now well appreciated that the developmental path toward exhaustion is composed of a heterogeneous pool of cells with varying degrees of effector potential that ultimately converge on a terminally differentiated state. Recent description of the developmental stages along the differentiation trajectory of T cell exhaustion has provided insight into past immunotherapeutic success and future opportunities. Here, we discuss the hallmarks of distinct developmental stages occurring along the path to T cell dysfunction and the impact of these discrete CD8 T cell fates on cancer immunotherapy.
三十年的基础研究探索了促进 T 细胞耗竭的分子和细胞机制,现在能够为基于 T 细胞的治疗慢性感染和癌症的疗法进行合理设计。曾经被描述为一种静态的细胞命运,现在人们已经充分认识到,通向耗竭的发育途径由具有不同效应潜力的异质细胞池组成,最终趋同于终末分化状态。最近对 T 细胞耗竭分化轨迹上的发育阶段的描述提供了对过去免疫治疗成功和未来机会的深入了解。在这里,我们讨论了沿着 T 细胞功能障碍路径发生的不同发育阶段的特征,以及这些离散的 CD8 T 细胞命运对癌症免疫治疗的影响。