Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Front Immunol. 2021 Mar 19;11:624199. doi: 10.3389/fimmu.2020.624199. eCollection 2020.
Resident memory CD8 T (T) cells are a lymphocyte lineage distinct from circulating memory CD8 T cells. T lodge within peripheral tissues and secondary lymphoid organs where they provide rapid, local protection from pathogens and control tumor growth. However, dysregulation of CD8 T formation and/or activation may contribute to the pathogenesis of autoimmune diseases. Intrinsic mechanisms, including transcriptional networks and inhibitory checkpoint receptors control T differentiation and response. Additionally, extrinsic stimuli such as cytokines, cognate antigen, fatty acids, and damage signals regulate T formation, maintenance, and expansion. In this review, we will summarize knowledge of CD8 T generation and highlight mechanisms that regulate the persistence and responses of heterogeneous T populations in different tissues and distinct microenvironments.
常驻记忆性 CD8 T(T)细胞是一种与循环记忆性 CD8 T 细胞不同的淋巴细胞谱系。T 细胞驻留在外周组织和次级淋巴器官中,在那里它们提供对病原体的快速、局部保护,并控制肿瘤生长。然而,CD8 T 细胞形成和/或激活的失调可能导致自身免疫性疾病的发病机制。内在机制,包括转录网络和抑制性检查点受体,控制 T 细胞的分化和反应。此外,外在刺激,如细胞因子、同源抗原、脂肪酸和损伤信号,调节 T 细胞的形成、维持和扩增。在这篇综述中,我们将总结 CD8 T 细胞生成的知识,并强调调节不同组织和不同微环境中异质性 T 细胞群体的持久性和反应的机制。