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
药品
生物化学
作者
Teng Ma,Danqi Li,Zhuo-Ran Yang,Qi Wang,Rong Chen,Niannian Lv,Kehan Du,Huimin Qin,Juan Tao,Hao Jiang,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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