树突状细胞
免疫
胰腺癌
获得性免疫系统
肿瘤微环境
CD8型
T细胞
CD40
免疫疗法
调节性T细胞
免疫学
免疫系统
生物
癌症
癌症研究
白细胞介素2受体
细胞毒性T细胞
遗传学
体外
生物化学
作者
Graham D. Hogg,Alyssa G. Weinstein,Natalie L. Kingston,Xiuting Liu,Olivia M. Dres,Liang‐I Kang,Varintra E. Lander,Yu‐Lan Kao,Faiz Ahmad,Brett L. Knolhoff,Varun Shenoy,Blake Sells,Reyka G. Jayasinghe,Andrew Houston,Tiantian Liu,John M. Herndon,Kenneth M. Murphy,Li Ding,Ryan C. Fields,Roheena Z. Panni
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2025-08-15
卷期号:10 (110): eadp3978-eadp3978
被引量:12
标识
DOI:10.1126/sciimmunol.adp3978
摘要
T cell expansion, and in turn, T cell-derived IFN-γ enhanced cDC1 survival. Nevertheless, Flt3L and CD40 agonism increased regulatory T cells through the activation of cDC2s, dampening immunity. These findings advocate further exploration of DC-centered approaches to enhance antitumor immunity in PDAC.
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