Abstract |
Dendritic cell vaccine (DCV) holds great potential in tumor immunotherapy owing to its potent ability in eliciting tumor-specific immune responses. Aiming at engineering enhanced DCV, we report the first effort to construct a glycopolymer-engineered DC vaccine (G-DCV) via metabolicglycoengineering and copper-free click-chemistry. Model G-DCV was prepared by firstly delivering tumor antigens, ovalbumin (OVA) into dendritic cells (DC) with fluoroalkane-grafted polyethyleneimines, followed by conjugating glycopolymers with a terminal group of dibenzocyclooctyne (DBCO) onto dendritic cells. Compared to unmodified DCV, our G-DCV could induce stronger T cell activation due to the enhanced adhesion between DCs and T cells. Notably, such G-DCV could more effectively inhibit the growth of the mouse B16-OVA (expressing OVA antigen) tumor model after adoptive transfer. Moreover, by combination with an immune checkpoint inhibitor, G-DCV showed further increased anti- tumor effects in treating different tumor models. Thus, our work provides a novel strategy to enhance the therapeutic effectiveness of DC vaccines.
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Authors | He Yang, Zijian Xiong, Xingyu Heng, Xiaomeng Niu, Yichen Wang, Lihua Yao, Lele Sun, Zhuang Liu, Hong Chen |
Journal | Angewandte Chemie (International ed. in English)
(Angew Chem Int Ed Engl)
Vol. 63
Issue 2
Pg. e202315782
(Jan 08 2024)
ISSN: 1521-3773 [Electronic] Germany |
PMID | 38018480
(Publication Type: Journal Article)
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Copyright | © 2023 Wiley-VCH GmbH. |
Chemical References |
- Antigens, Neoplasm
- Ovalbumin
- Vaccines
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Topics |
- Mice
- Animals
- T-Lymphocytes
- Antigens, Neoplasm
- Neoplasms
(metabolism)
- Ovalbumin
- Cell Membrane
- Dendritic Cells
(metabolism)
- Vaccines
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