癌症免疫疗法
电穿孔
癌症研究
免疫疗法
化学
信使核糖核酸
适体
癌细胞
体内
癌症治疗
免疫系统
转染
淋巴结
免疫原性
嵌合抗原受体
癌症治疗
前药
抗原
指南针
癌症
树突状细胞
分子生物学
细胞凋亡
细胞生物学
生物
癌症疫苗
内体
靶向治疗
医学
作者
Xueliang Liu,Yuqing Li,Xinfeng Dai,Zhicheng Huang,Jiabei Li,Chuhuang Dong,Ziliang Dong,Dali Wei,Huayuan Zhou,Zhuang Liu,Yu Yang,Weihong Tan
标识
DOI:10.1002/anie.202519216
摘要
Abstract mRNA vaccines hold remarkable promise for cancer immunotherapy, yet current nanoparticle systems face challenges in efficacy, dendritic cell (DC) targeting, and safety. Herein, we report a nanoplatform, Manganese‐Coordinated Polyvalent Aptameric System (COMPASS), enabling targeted co‐delivery of mRNA and Mn 2 + to lymph node dendritic cells (DC) to boost potent antitumor immunity. The COMPASS employed rolling circle amplification to generate single‐stranded DNA scaffolds with multivalent DC‐targeting aptamers and polyT domains, enabling stable mRNA hybridization via A‐T pairing. Various metal ions were screened, and Mn 2 + was found to enhance mRNA endosomal escape and activate the STING pathway in DCs, promoting their maturation and antigen presentation. Controlled nanoparticle size (∼200 nm) and aptamer‐mediated DC targeting markedly enhanced lymphatic accumulation. In vivo evaluations revealed that COMPASS achieved potent prophylactic and therapeutic antitumor efficacy comparable to commercial LNPs (e.g., SM‐102), while exhibiting significantly enhanced safety profiles. Importantly, lyophilized COMPASS formulations retained their structural integrity and bioactivity for at least three months at room temperature. Overall, COMPASS represents a promising next‐generation nanoplatform with significant translational potential for safe and effective cancer immunotherapy.
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