Mempel Thorsten R, Malehmir Mohsen
Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Curr Opin Immunol. 2025 Feb;92:102510. doi: 10.1016/j.coi.2024.102510. Epub 2024 Dec 11.
Local regulation of T cell-mediated immunity to solid tumors occurs at multiple levels, including their recruitment from the bloodstream to the tumor microenvironment (TME), coordinated crosstalk with different subsets of antigen-presenting cells (APCs) controlling their local survival, proliferation, and effector differentiation, as well as their egress from tumors via lymphatics. At each level, chemokines play essential roles, for instance, by guiding directional T cell migration across blood and lymphatic endothelial barriers or by promoting their spatial proximity and direct physical interactions with APCs to enable functional crosstalk. In this article, we will review recent mechanistic insights into the chemokine axes that guide T cell functions in TMEs in light of the emerging functional state heterogeneity of CD8 effector T cells and our growing understanding of how regulatory T cells restrain antitumor activity.
T细胞介导的针对实体瘤免疫的局部调节发生在多个层面,包括从血液招募至肿瘤微环境(TME)、与不同亚群的抗原呈递细胞(APC)进行协调串扰以控制其局部存活、增殖和效应分化,以及通过淋巴管从肿瘤中逸出。在每个层面,趋化因子都发挥着重要作用,例如,引导T细胞定向迁移穿过血液和淋巴管内皮屏障,或促进其与APC在空间上的接近以及直接的物理相互作用,以实现功能性串扰。在本文中,鉴于CD8效应T细胞新出现的功能状态异质性以及我们对调节性T细胞如何抑制抗肿瘤活性的日益了解,我们将综述关于趋化因子轴引导TME中T细胞功能的最新机制见解。