癌症免疫疗法
免疫疗法
癌症研究
免疫系统
化学
癌细胞
抗原
细胞生物学
抗原提呈细胞
纳米技术
T细胞
癌症
生物
免疫学
材料科学
遗传学
作者
Ping Xiao,Jue Wang,Zitong Zhao,Xiaochen Liu,Xiangshi Sun,Dangge Wang,Yaping Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-02-24
卷期号:21 (5): 2094-2103
被引量:64
标识
DOI:10.1021/acs.nanolett.0c04783
摘要
Nanoscale artificial antigen-presenting cells (aAPCs) are promising to activate T cells directly for cancer immunotherapy, while feasible and flexible strategy to develop nanoscale aAPCs remains highly desirable. Metabolic glycoengineering is used to decorate chemical tags on cells which enables bioorthogonal chemical conjugation of functional molecules. Herein, we develop a nanoscale aAPC by metabolic dendritic cell (DC) labeling to mobilize T-cell based antitumor immunity. We coat azido-labeled DC membrane on imiquimod-loaded polymeric nanoparticles and sequentially modify anti-CD3ε antibody via click chemistry. The nanoscale aAPCs perform improved distribution in lymph nodes and stimulate T cells and resident APCs. Significant inhibition of tumor inoculation and growth is observed after the vaccination, which can be further improved by combining antiprogrammed cell death receptor 1 (PD1) therapy. Our results demonstrate the promising application of metabolically labeled DCs for designing nanoscale aAPCs, which provide a simple and general strategy to potentiate cancer immunotherapy.
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