A rationally designed cancer vaccine based on NIR-II fluorescence image-guided light-triggered remote control of antigen cross-presentation and autophagy

被引:0
|
作者
Aihua Wu [1 ]
Afeng Yang [1 ]
Qinli Tong [1 ]
Guoguang Wei [1 ]
Sihang Zhang [1 ]
Sheng Yu [1 ]
Chen Zhang [1 ]
Jiaojiao Xu [1 ]
Wei Lu [1 ]
机构
[1] School of Pharmacy & Minhang Hospital, Key Laboratory of Smart Drug Delivery, Ministry of Education, & State Key Laboratory of Molecular Engineering of Polymers, Fudan University
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TQ464 [生物制品药物的生产]; R730.51 [免疫疗法];
学科分类号
100214 ; 100705 ;
摘要
Cancer vaccines represent a promising immunotherapeutic treatment modality. The promotion of cross-presentation of extracellular tumor-associated antigens on the major histocompatibility complex(MHC) class I molecules and dendritic cell maturation at the appropriate time and place is crucial for cancer vaccines to prime cytolytic T cell response with reduced side effects. Current vaccination strategies, however, are not able to achieve the spatiotemporal control of antigen cross-presentation. Here, we report a liposomal vaccine loading the second near-infrared window(NIR-II, 1000—1700 nm) fluorophore BPBBT with an efficient photothermal conversion effect that offers an NIR-light-triggered endolysosomal escape under the imaging guidance. The NIR-II image-guided vaccination strategy specifically controls the cytosolic delivery of antigens for cross-presentation in the draining lymph nodes(DLNs). Moreover, the photothermally induced endolysosomal rupture initiates autophagy. We also find that the adjuvant simvastatin acts as an autophagy activator through inhibiting the PI3K/AKT/m TOR pathway. The light-induced autophagy in the DLNs together with simvastatin treatment cooperatively increase MHC class II expression by activating autophagy machinery for dendritic cell maturation. This study presents a paradigm of NIR-II image-guided light-triggered vaccination. The approach for remote control of antigen cross-presentation and autophagy represents a new strategy for vaccine development.
引用
收藏
页码:3121 / 3136
页数:16
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