Department of Molecular Biology, School of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Immunol Rev. 2023 Jul;316(1):8-22. doi: 10.1111/imr.13218. Epub 2023 May 16.
Cytotoxic CD8 T cells recognize and eliminate infected or cancerous cells. A subset of CD8 memory T cells called tissue-resident memory T cells (T ) resides in peripheral tissues, monitors the periphery for pathogen invasion, and offers a rapid and potent first line of defense at potential sites of re-infection. T cells are found in almost all tissues and are transcriptionally and epigenetically distinct from circulating memory populations, which shows their ability to acclimate to the tissue environment to allow for long-term survival. Recent work and the broader availability of single-cell profiling have highlighted T heterogeneity among different tissues, as well as identified specialized subsets within individual tissues, that are time and infection dependent. T cell phenotypic and transcriptional heterogeneity has implications for understanding T function and longevity. This review aims to summarize and discuss the latest findings on CD8 T heterogeneity using single-cell molecular profiling and explore the potential implications for immune protection and the design of immune therapies.
细胞毒性 CD8 T 细胞识别并清除受感染或癌变的细胞。称为组织驻留记忆 T 细胞 (T ) 的 CD8 记忆 T 细胞亚群存在于外周组织中,监测外周组织中病原体的入侵,并在潜在的再感染部位提供快速而有效的第一道防线。T 细胞几乎存在于所有组织中,在转录和表观遗传上与循环记忆群体不同,这表明它们能够适应组织环境以实现长期存活。最近的工作和单细胞分析的广泛应用突出了不同组织之间 T 细胞的异质性,并确定了个体组织内的专门亚群,这些亚群依赖于时间和感染。T 细胞表型和转录组异质性对理解 T 细胞功能和寿命具有重要意义。本综述旨在总结和讨论使用单细胞分子分析技术研究 CD8 T 细胞异质性的最新发现,并探讨其对免疫保护和免疫治疗设计的潜在影响。