佐剂
癌症免疫疗法
免疫疗法
先天免疫系统
抗原
癌症
细胞毒性
免疫系统
癌症研究
免疫学
生物
体外
生物化学
遗传学
作者
Xuanbo Zhang,Kaiyuan Wang,Zhiqiang Zhao,Xinzhu Shan,Yuequan Wang,Zunyong Feng,Bingyu Li,Cong Luo,Xiaoyuan Chen,Jin Sun
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-02-26
卷期号:18 (9): 7136-7147
被引量:6
标识
DOI:10.1021/acsnano.3c11637
摘要
Tapping into the innate immune system's power, nanovaccines can induce tumor-specific immune responses, which is a promising strategy in cancer immunotherapy. However, traditional vaccine design, requiring simultaneous loading of antigens and adjuvants, is complex and poses challenges for mass production. Here, we developed a tumor nanovaccine platform that integrates adjuvant functions into the delivery vehicle, using branched polyguanidine (PolyGu) nanovaccines. These nanovaccines were produced by modifying polyethylenimine (PEI) with various guanidine groups, transforming PEI's cytotoxicity into innate immune activation. The PolyGu nanovaccines based on poly(phenyl biguanidine ) (Poly-PBG) effectively stimulated dendritic cells, promoted their maturation via the TLR4 and NLRP3 pathways, and displayed robust in vivo immune activity. They significantly inhibited tumor growth and extended mouse survival. The PolyGu also showed promise for constructing more potent mRNA-based nanovaccines, offering a platform for personalized cancer vaccine. This work advances cancer immunotherapy toward potential clinical application by introducing a paradigm for developing self-adjuvanting nanovaccines.
科研通智能强力驱动
Strongly Powered by AbleSci AI