前药
免疫原性细胞死亡
免疫系统
肿瘤微环境
光动力疗法
癌症研究
连接器
化学
癌细胞
免疫疗法
癌症免疫疗法
医学
癌症
免疫学
肿瘤细胞
生物化学
有机化学
内科学
操作系统
计算机科学
作者
Jiaping Shen,Bin Xu,Yun Zheng,Xingyu Zhao,Huixuan Qi,Yongan Tang,Wenhai Lin,Shengliang Li,Zhiyuan Zhong
标识
DOI:10.1002/ange.202425309
摘要
Light‐activatable prodrugs have been applied in precision cancer therapy because of their spatiotemporal controllability and minimal toxic side effects. However, the reported prodrugs were limited by the ultraviolet and visible light regions, which seriously restricted their application in deep tissues. Developing a near‐infrared (NIR) light‐activatable release system remains a great challenge. Herein, the 808 nm light‐activatable prodrugs were constructed with imiquimod (R837) and NIR boron dipyrromethene (BODIPY) via a reactive oxygen species (ROS)‐cleavable linker for photoimmunotherapy of “cold” cancer. ROS produced by BODIPY could cleave the linker under 808 nm laser irradiation, and R837 was released spatiotemporally at the tumor site. The combination of the immune response produced by R837 and immunogenic cell death caused by phototherapy significantly potentiated adaptive antitumor immunity and enhanced cytotoxic CD8+ T cell infiltration for tumor metastasis and distant tumor inhibition. This work provides an effective NIR light‐activatable controlled release system for cancer immunotherapy and metastasis suppression.
科研通智能强力驱动
Strongly Powered by AbleSci AI