溶瘤病毒
免疫疗法
癌症研究
癌症免疫疗法
T细胞
病毒
肿瘤细胞
化学
肿瘤微环境
细胞凋亡
细胞
病毒学
生物
免疫系统
免疫学
生物化学
作者
Fan Wu,Yanli Li,Yun Meng,Xuechao Cai,Jieyun Shi,Jinjin Li,Yang Chen,Li Zhang,Xianfu Meng,Huiyan Li,Xingwu Jiang,Zhenxiao Fu,Yelin Wu,Wenbo Bu
标识
DOI:10.1002/anie.202210487
摘要
T lymphocytes (T cells) are essential for tumor immunotherapy. However, the insufficient number of activated T cells greatly limits the efficacy of tumor immunotherapy. Herein, we proposed an oncolytic virus-mimicking strategy to enhance T cell recruitment and activation for tumor treatment. We constructed an oncolytic virus-like nanoplatform (PolyIC@ZIF-8) that was degraded in the acidic tumor environment to release PolyIC and Zn2+ . The released PolyIC exhibited an oncolytic virus-like function that induced tumor cell apoptosis and promoted T cell recruitment and activation through a tumor antigen-dependent manner. More importantly, the released Zn2+ not only enhanced T cell recruitment by inducing CXCL9/10/11 expression but also promoted T cell activation to increase interferon-γ (INF-γ) expression by inducing the phosphorylation of ZAP-70 via a tumor antigen-independent manner. This Zn2+ -enhanced oncolytic virus-mimicking strategy provides a new approach for tumor immunotherapy.
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