内体
兴奋剂
TLR7型
受体
化学
癌症免疫疗法
细胞生物学
Toll样受体
免疫系统
癌症研究
免疫疗法
生物
药理学
生物化学
先天免疫系统
免疫学
作者
Heming Xia,Mengmeng Qin,Zenghui Wang,Yaoqi Wang,Binlong Chen,Fangjie Wan,Mingmei Tang,Xingquan Pan,Ye Yang,Jianxiong Liu,Ruiyang Zhao,Qiang Zhang,Yiguang Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-03-18
卷期号:22 (7): 2978-2987
被引量:55
标识
DOI:10.1021/acs.nanolett.2c00185
摘要
Toll-like receptor (TLR) agonists are potent immune-stimulators that hold great potential in vaccine adjuvants as well as cancer immunotherapy. However, TLR agonists in free form are prone to be eliminated quickly by the circulatory system and cause systemic inflammation side effects. It remains a challenge to achieve precise release of TLR7/8 agonist in the native form at the receptor site in the endosomal compartments while keeping stable encapsulation and inactive in nontarget environment. Here, we report a pH-/enzyme-responsive TLR7/8 agonist-conjugated nanovaccine (TNV), which responds intelligently to the acidic environment and cathepsin B in the endosome, precisely releases TLR7/8 agonist to activate its receptor signaling at the endosomal membrane, stimulates DCs maturation, and provokes specific cellular immunity. In vivo experiments demonstrate outstanding prophylactic and therapeutic efficacy of TNV in mouse melanoma and colon cancer. The endosome-targeted responsive nanoparticle strategy provides a potential delivery toolbox of adjuvants to advance the development of tumor nanovaccines.
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