State Key Laboratory of Drug Research and Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Nano Lett. 2021 Mar 10;21(5):2094-2103. doi: 10.1021/acs.nanolett.0c04783. Epub 2021 Feb 23.
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.
纳米级人工抗原呈递细胞(aAPCs)有望直接激活 T 细胞用于癌症免疫治疗,而开发纳米级 aAPCs 的可行且灵活的策略仍然非常需要。代谢糖基工程用于在细胞上修饰化学标记物,从而能够进行功能性分子的生物正交化学偶联。在此,我们通过代谢树突状细胞(DC)标记来开发纳米级 aAPC,以调动基于 T 细胞的抗肿瘤免疫。我们在负载咪喹莫特的聚合物纳米颗粒上涂覆叠氮标记的 DC 膜,并通过点击化学顺序修饰抗 CD3ε 抗体。纳米级 aAPC 在淋巴结中的分布得到改善,并刺激 T 细胞和固有 APC。接种后观察到肿瘤接种和生长的显著抑制,通过结合抗程序性细胞死亡受体 1(PD1)治疗可以进一步改善。我们的结果表明,代谢标记的 DC 可用于设计纳米级 aAPC,为增强癌症免疫治疗提供了一种简单而通用的策略。