Piao Wenji, Lee Zachariah L, Zapas Gregory, Wu Long, Jewell Christopher M, Abdi Reza, Bromberg Jonathan S
Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.
Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, USA.
Nat Rev Immunol. 2025 Apr 1. doi: 10.1038/s41577-025-01149-2.
Regulatory T (T) cells have a central role in the maintenance of immune surveillance and tolerance. They can migrate from lymphoid organs to blood and then into tissues and egress from tissues into draining lymph nodes. Specialized endothelial cells of blood and lymphatic vessels are the key gatekeepers for these processes. T cells that transmigrate across single-cell layers of endothelial cells engage in bidirectional crosstalk with these cells and regulate vascular permeability by promoting structural modifications of blood and lymphatic endothelial cells. In turn, blood and lymphatic endothelial cells can modulate T cell recirculation and residency. Here, we discuss recent insights into the cellular and molecular mechanisms of the crosstalk between T cells and endothelial cells and explore potential therapeutic strategies to target these interactions in autoimmunity, transplantation and cancer.
调节性T(Treg)细胞在维持免疫监视和免疫耐受中发挥着核心作用。它们可从淋巴器官迁移至血液,进而进入组织,并从组织进入引流淋巴结。血液和淋巴管的特化内皮细胞是这些过程的关键守门人。穿越内皮细胞单细胞层迁移的T细胞与这些细胞进行双向串扰,并通过促进血液和淋巴管内皮细胞的结构改变来调节血管通透性。反过来,血液和淋巴管内皮细胞可调节T细胞的再循环和驻留。在此,我们讨论了关于T细胞与内皮细胞之间串扰的细胞和分子机制的最新见解,并探索了针对自身免疫、移植和癌症中这些相互作用的潜在治疗策略。