化学
药物输送
免疫系统
靶向给药
细胞生物学
药品
小泡
细胞外小泡
输送系统
纳米技术
药理学
基因传递
药物发现
毒品携带者
体内
细胞培养
微泡
作者
Fang Zhou,Saichao Wei,S Wang,Jiaqi Xu,M Zhang,Mingyu Yin,Jun Wang,Kehai Liu
标识
DOI:10.1186/s12951-026-04699-2
摘要
To overcome the critical challenges of insufficient drug targeting and restricted dendritic cell (DC) activation in chemo-immunotherapy, this study developed an innovative cross-species hybrid vesicle delivery system. By fusing extracellular vesicles derived from 4T1 tumor cells (TEV) with kiwifruit-derived extracellular vesicles (KEV), we constructed a homologous targeting hybrid vesicle carrier (TKEV). This platform was co-loaded with chemotherapeutic agent doxorubicin (DOX) and Bcl-2 siRNA (siBcl2) to form a combination therapeutic system (TKDS). Key findings demonstrate: (1) TKDS achieves precise tumor-targeted delivery, significantly enhancing tumor cell apoptosis through combined chemo-gene therapy; (2) The KEV component effectively stimulated DC maturation, enhanced antigen presentation, and increased CD8+ T cell infiltration in tumors; (3) In a 4T1 murine breast cancer models, TKDS significantly enhanced antitumor efficacy through synergistic immunochemotherapy. To our knowledge, this work provides the first evidence that a cross-species vesicle fusion strategy can simultaneously enhance drug targeting and immune activation, offering a versatile and promising platform for developing highly effective and safer immunochemotherapy regimens.
科研通智能强力驱动
Strongly Powered by AbleSci AI