纳米器件
适体
纳米技术
DNA
免疫疗法
癌症免疫疗法
免疫系统
寡核苷酸
Toll样受体9
肿瘤微环境
癌症研究
免疫刺激剂
化学
材料科学
免疫学
生物
生物化学
基因
分子生物学
DNA甲基化
基因表达
作者
Dejie Lu,Zhenghan Di,Lele Li,Jian Zhao,Li Zheng
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-04-30
卷期号:17 (10): 9078-9083
被引量:6
标识
DOI:10.1007/s12274-024-6632-3
摘要
Efficient delivery of therapeutics to immune cells remains a formidable challenge for cancer immunotherapy. In this work, we demonstrate that an aptamer-driven DNA nanodevice, constructed through linkage of a synthetic immunostimulant (Toll-like receptor 9 agonist: CpG motif) to an aptamer, could significantly enhance the immunostimulatory activity by facilitating the uptake and retention of therapeutics in macrophages. Systemic administration of the DNA nanodevice results in efficient tumor growth inhibition in both breast cancer and melanoma mouse models. Our studies suggest that the DNA nanodevice leads to reeducation of tumor-associated macrophages and ultimately to reversing the tumor immune microenvironment. The strategy for aptamer-mediated and vehicle-free delivery of immunostimulatory oligonucleotides provides a potential platform for cancer immunotherapy.
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