头颈部鳞状细胞癌
毛皮
化学
免疫原性细胞死亡
细胞生物学
原卟啉IX
光敏剂
高尔基体
癌症研究
程序性细胞死亡
细胞
光动力疗法
生物
头颈部癌
生物化学
细胞凋亡
癌症
有机化学
遗传学
酶
作者
Zhi-Hang Zhou,Xin‐yu Zhou,Yi‐yi Zhang,Tongchao Zhao,Jiang Li,Lai‐ping Zhong,Yichuan Pang
标识
DOI:10.1002/adhm.202400012
摘要
Abstract Head and neck carcinoma treatment is shifted toward the combination of therapy causing immune checkpoint blockade (ICB) and immunogenic cell death. In this study, a CSFRi‐chimeric TAM CSFR+ ‐targeting extracellular vesicle (EV@CSFRi) platform is developed and designed an intracellular protoporphyrin conjugated with RVRR peptide sequence for furin‐cleavage to perform Golgi‐targeting and generating ROS (GT‐RG). The graphical abstract illustrates the self‐assembly of GT‐RG nanoparticles into nanofiber through the hydrophily of RVRR and hydrophobicity of RG, and the red line indicates the site of furin cleavage. As is shown in the Graphical abstract, the Golgi‐targeting Protoporphyrin‐RVRR platform is composed with CSFRi‐chimeric extracellular vesicles and forms the tumor‐responsive TAM‐reprogramming bilayers (GT‐RG EV @CSFRi). The GT‐RG EV @CSFRi acted as a multifunctional theranostic platform, which can induce immunogenic cell death and further help modulate TAM, thus suppressing the HNC xenograft model by combination therapy with anti‐PD‐1.
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