封锁
免疫检查点
细胞毒性T细胞
肿瘤微环境
免疫系统
CD8型
T细胞
胶质瘤
生物
癌症研究
CXCR3型
免疫学
免疫疗法
趋化因子
趋化因子受体
受体
体外
生物化学
作者
Haofei Liu,Qiwen Zhao,Leyong Tan,Xin Wu,Rui Huang,Yonglin Zuo,Longjuan Chen,Ji-gui Yang,Zuo‐Xin Zhang,Wenchen Ruan,Jiayang Wu,Fei He,Yiliang Fang,Fangyuan Mao,Peipei Zhang,Xiaoning Zhang,Peidi Yin,Zexuan Yan,Wenwen Xu,Huimin Lu
出处
期刊:Cancer Cell
[Cell Press]
日期:2023-03-23
卷期号:41 (4): 693-710.e8
被引量:132
标识
DOI:10.1016/j.ccell.2023.03.004
摘要
T, myeloid, and tumor cells orchestrate myeloid-derived suppressor cell infiltration and angiogenesis, which results in enhanced tumor growth but reduced ICB efficacy. Antibody-mediated IL-8 blockade or the inhibition of its receptor, CXCR1/2, unleashes anti-PD-1-mediated antitumor immunity. Our findings thus highlight IL-8 as a combinational immunotherapy target for glioma.
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