细胞毒性T细胞
CD8型
T细胞
癌症研究
生物
细胞因子
免疫系统
白细胞介素2受体
细胞生物学
腺苷受体
免疫学
化学
干扰素γ
嘌呤能信号
腺苷
腺苷A3受体
促炎细胞因子
白细胞介素15
作者
Altay Koyas,Suat Tucer,Merve Kayhan,Ali Can Savas,Imran Akdemir,Caglar Cekic
出处
期刊:Science Signaling
[American Association for the Advancement of Science (AAAS)]
日期:2021-03-16
卷期号:14 (674)
被引量:3
标识
DOI:10.1126/scisignal.abb1269
摘要
The nucleoside adenosine accumulates extracellularly in solid tumors and inhibits CD8+ T cells by activating adenosine receptors. The cytokine interleukin-7 (IL-7), which is produced by various tissues and tumors, promotes the survival and maintenance of T cells. Adenosine and IL-7 signaling are being clinically targeted separately or in combination with other therapies for solid tumor indications. Here, we found that IL-7 signaling promoted the accumulation of tumor-associated CD8+ T cells, in part, by preventing adenosine-mediated immunosuppression. Inhibition of the transcription factor FoxO1 downstream of IL-7 receptor signaling was important for protecting CD8+ T cells from suppression by adenosine. These findings have implications for the development of new approaches for cancer immunotherapies that target the adenosine pathway.
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