生物
自身免疫
白细胞介素2受体
细胞毒性T细胞
T细胞
CD8型
癌症免疫疗法
细胞因子
免疫学
白细胞介素15
癌症研究
免疫疗法
细胞生物学
白细胞介素
免疫系统
遗传学
体外
作者
Acacia N. Shouse,Kathryn M LaPorte,Thomas R. Malek
出处
期刊:Immunity
[Elsevier]
日期:2024-03-01
卷期号:57 (3): 414-428
被引量:9
标识
DOI:10.1016/j.immuni.2024.02.001
摘要
Summary
Interleukin-2 (IL-2) is a critical cytokine for T cell peripheral tolerance and immunity. Here, we review how IL-2 interaction with the high-affinity IL-2 receptor (IL-2R) supports the development and homeostasis of regulatory T cells and contributes to the differentiation of helper, cytotoxic, and memory T cells. A critical element for each T cell population is the expression of CD25 (Il2rα), which heightens the receptor affinity for IL-2. Signaling through the high-affinity IL-2R also reinvigorates CD8+ exhausted T (Tex) cells in response to checkpoint blockade. We consider the molecular underpinnings reflecting how IL-2R signaling impacts these various T cell subsets and the implications for enhancing IL-2-dependent immunotherapy of autoimmunity, other inflammatory disorders, and cancer.
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