Division of Molecular Oncology and Immunology, Oncode Institute, The Netherlands Cancer Institute, 1066 Amsterdam, the Netherlands.
Cold Spring Harb Perspect Biol. 2021 Aug 2;13(8):a038117. doi: 10.1101/cshperspect.a038117.
Resident memory CD8 T (Trm) cells permanently reside in nonlymphoid tissues where they act as a first line of defense against recurrent pathogens. How and when antigen-inexperienced CD8 T cells differentiate into Trm has been a topic of major interest, as knowledge on how to steer this process may be exploited in the development of vaccines and anticancer therapies. Here, we first review the current understanding of the early signals that CD8 T cells receive before they have entered the tissue and that govern their capacity to develop into tissue-resident memory T cells. Subsequently, we discuss the tissue-derived factors that promote Trm maturation in situ. Combined, these data sketch a model in which a subset of responding T cells develops a heightened capacity to respond to local cues present in the tissue microenvironment, which thereby imprints their ability to contribute to the tissue-resident memory CD8 T-cell pool that provide local control against pathogens.
常驻记忆 CD8 T(Trm)细胞永久存在于非淋巴组织中,它们是抵抗复发性病原体的第一道防线。抗原未经验证的 CD8 T 细胞如何以及何时分化为 Trm 一直是一个主要研究课题,因为了解如何引导这一过程可能会被应用于疫苗和抗癌疗法的开发。在这里,我们首先回顾了 CD8 T 细胞在进入组织之前接收到的早期信号的现有理解,这些信号决定了它们发展为组织驻留记忆 T 细胞的能力。随后,我们讨论了促进 Trm 原位成熟的组织衍生因子。综合这些数据,我们可以构建一个模型,其中一部分反应性 T 细胞发展出对组织微环境中存在的局部线索的更高反应能力,从而赋予它们为提供局部病原体控制的组织驻留记忆 CD8 T 细胞池做出贡献的能力。