佐剂
卵清蛋白
抗原
癌症免疫疗法
免疫疗法
免疫系统
癌症研究
免疫增强剂
免疫原
癌症
化学
CD8型
免疫学
生物
医学
抗体
内科学
单克隆抗体
作者
Zhen-Lin Gao,Wei Xu,Sui-Juan Zheng,Qi-Jia Duan,Rong Liu,Jin‐Zhi Du
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-02-21
卷期号:23 (5): 1904-1913
被引量:27
标识
DOI:10.1021/acs.nanolett.2c04970
摘要
Cancer vaccines have received tremendous attention in cancer immunotherapy due to their capability to induce a tumor-specific immune response. However, their effectiveness is compromised by the insufficient spatiotemporal delivery of antigens and adjuvants in the subcellular level to induce a robust CD8+ T cell response. Herein, a cancer nanovaccine G5-pBA/OVA@Mn is prepared through multiple interactions of manganese ions (Mn2+), benzoic acid (BA)-modified fifth generation polyamidoamine (G5-PAMAM) dendrimer, and the model protein antigen ovalbumin (OVA). In the nanovaccine, Mn2+ not only exerts a structural function to assist OVA loading as well as its endosomal escape, but works as an adjuvant of stimulator of interferon genes (STING) pathway. These collaboratively facilitate the orchestrated codelivery of OVA antigen and Mn2+ into cell cytoplasm. Vaccination with G5-pBA/OVA@Mn not only shows a prophylactic effect, but also significantly inhibits growth against B16-OVA tumors, indicating its great potential for cancer immunotherapy.
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