Wu Aihua, Yang Afeng, Tong Qinli, Wei Guoguang, Zhang Sihang, Yu Sheng, Zhang Chen, Xu Jiaojiao, Lu Wei
School of Pharmacy & Minhang Hospital, Key Laboratory of Smart Drug Delivery, Ministry of Education, & State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai 201203, China.
Acta Pharm Sin B. 2023 Jul;13(7):3121-3136. doi: 10.1016/j.apsb.2022.11.027. Epub 2022 Dec 1.
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/mTOR 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.
癌症疫苗是一种很有前景的免疫治疗方式。在适当的时间和地点促进细胞外肿瘤相关抗原在主要组织相容性复合体(MHC)I类分子上的交叉呈递以及树突状细胞成熟,对于癌症疫苗引发细胞溶解T细胞反应并减少副作用至关重要。然而,目前的疫苗接种策略无法实现对抗原交叉呈递的时空控制。在此,我们报告了一种负载具有高效光热转换效应的第二近红外窗口(NIR-II,1000 - 1700纳米)荧光团BPBBT的脂质体疫苗,该疫苗在成像引导下可实现近红外光触发的内溶酶体逃逸。NIR-II图像引导的疫苗接种策略特异性地控制抗原在引流淋巴结(DLN)中的胞质递送以进行交叉呈递。此外,光热诱导的内溶酶体破裂引发自噬。我们还发现佐剂辛伐他汀通过抑制PI3K/AKT/mTOR途径作为自噬激活剂。DLN中光诱导的自噬与辛伐他汀治疗协同作用,通过激活树突状细胞成熟的自噬机制共同增加MHC II类分子的表达。本研究提出了一种NIR-II图像引导的光触发疫苗接种模式。这种远程控制抗原交叉呈递和自噬的方法代表了一种新的疫苗开发策略。