自噬
肿瘤微环境
免疫疗法
癌症研究
光动力疗法
免疫原性细胞死亡
免疫原性
癌症免疫疗法
线粒体
细胞毒性T细胞
细胞凋亡
化学
免疫系统
免疫学
生物
肿瘤细胞
细胞生物学
体外
生物化学
有机化学
作者
Hong Xiao,Xiaoxia Li,Bo Li,Shuguang Yang,Jingya Qin,Shisong Han,Jie Ren,Xintao Shuai
出处
期刊:Small
[Wiley]
日期:2023-04-14
卷期号:19 (30)
被引量:28
标识
DOI:10.1002/smll.202300280
摘要
Abstract Anticancer immunotherapy is hampered by the poor tumor immunogenicity and immunosuppressive tumor microenvironment (TME). Herein, a liposome nanodrug co‐encapsulating doxycycline hydrochloride (Doxy) and chlorin e6 (Ce6) to simultaneously induce autophagy inhibition and mitochondria dysfunction for potentiating tumor photo‐immunotherapy is developed. Under near infrared laser irradiation, Ce6 generates cytotoxic reactive oxygen species (ROS) and elicits robust photodynamic therapy (PDT)‐induced immunogenic cell death (ICD) for immunosuppressive TME remodeling. In addition, Doxy induced mitochondria dysfunction, which increases ROS generation and enhances PDT to exert more potent killing effect and more powerful ICD. Meanwhile, Doxy increases MHC‐I expression on tumor cells surface by efficient autophagy inhibition, leading to more efficient antigen presentation and CTLs recognition to increase tumor immunogenicity. The nanodrugs elicit remarkable antitumor therapy by combining Ce6‐mediated PDT and Doxy‐induced autophagy inhibition and mitochondria dysfunction. The developed nanodrugs represent a highly efficient strategy for improving cancer immunotherapy.
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