FOXP3型
生物
淋巴系统
细胞生物学
祖细胞
先天性淋巴细胞
再生(生物学)
表型
功能(生物学)
细胞分化
免疫学
调节性T细胞
免疫系统
白细胞介素2受体
T细胞
干细胞
免疫
遗传学
基因
作者
Andrés R. Muñoz-Rojas,Diane Mathis
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2021-03-26
卷期号:21 (9): 597-611
被引量:125
标识
DOI:10.1038/s41577-021-00519-w
摘要
The FOXP3+CD4+ regulatory T (Treg) cells located in non-lymphoid tissues differ in phenotype and function from their lymphoid organ counterparts. Tissue Treg cells have distinct transcriptomes, T cell receptor repertoires and growth and survival factor dependencies that arm them to survive and operate in their home tissue. Their functions extend beyond immune surveillance to tissue homeostasis, including regulation of local and systemic metabolism, promotion of tissue repair and regeneration, and control of the proliferation, differentiation and fate of non-lymphoid cell progenitors. Treg cells in diverse tissues share a common FOXP3+CD4+ precursor located within lymphoid organs. This precursor undergoes definitive specialization once in the home tissue, following a multilayered array of common and tissue-distinct transcriptional programmes. Our deepening knowledge of tissue Treg cell biology will inform ongoing attempts to harness Treg cells for precision immunotherapeutics.
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