自噬
纳米载体
免疫系统
癌症研究
免疫疗法
免疫原性细胞死亡
癌症免疫疗法
抗原呈递
树突状细胞
医学
化学
免疫学
T细胞
细胞凋亡
药理学
生物化学
药品
作者
Wei Ma,Danqi Li,Zhuoran Yang,Li Wang,Rong Chen,Niannian Lv,Kehan Du,Huimin Qin,Juan Tao,Hao Chen,Jintao Zhu
标识
DOI:10.1016/j.jconrel.2024.10.009
摘要
Mild autophagy accompanied with immunogenic cell death (ICD) effect destructs immune-associated antigens, weakening the immune response against tumor growth. To address this dilemma, we develop a peptide-based bicomponent nanocarrier with encapsulation of a cellular hyperautophagy activator (STF-62247) for near-infrared (NIR) photo/immunotherapy to eliminate primary and metastatic breast tumors. The electrostatic-driven nanodrug (PPNPs@STF) with active-targeting and efficient endosomal escape can induce specific ICD effect upon NIR laser irradiation, and trigger autophagy to a mild activation state. Notably, the simultaneously released STF-62247 precisely promotes autophagy to an overactivated state, resulting in autophagic death of tumor cells and further boosting ICD-related antigen presentation. More importantly, the combined photo/immunotherapy of PPNPs@STF not only inhibits tumor cell proliferation, but also promotes dendritic cells (DCs)-associated immune response. In 4 T1 tumor-bearing mice, PPNPs@STF effectively inhibits growth of primary and distant tumors, and suppresses lung metastasis with a minimized side effect. This study provides a hyperautophagy activator-assisted strategy that can enhance ICD-based antitumor immune response for the treatment of metastatic breast cancer.
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