癌症免疫疗法
抗原
癌症研究
癌症疫苗
免疫系统
先天免疫系统
免疫疗法
癌症
CD8型
免疫学
黑色素瘤
T细胞
生物
氮杂环丁烷
免疫
癌细胞
抗体
获得性免疫系统
淋巴
细胞毒性T细胞
树突状细胞
医学
接种疫苗
细胞
表位
信号转导衔接蛋白
受体
免疫耐受
化学
主动免疫治疗
抗原提呈细胞
作者
Junbin Chen,Miao Su,Boya Yu,Mingda Yang,Huiye Wang,X L Yang,Jun Wang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-03-20
卷期号:12 (12): eaeb2465-eaeb2465
标识
DOI:10.1126/sciadv.aeb2465
摘要
Therapeutic cancer vaccines show great promise for de novo induction of antigen-specific T cell responses against tumors. However, weak coordination between innate immune activation and antigen delivery remains a major obstacle to vaccine efficacy. Here, we present a cholesterol azetidine derivative-assisted polymeric carrier, Aze-Chol NP, which stimulates innate immunity and primes tumor-specific CD8+ T cell responses. Mechanistically, Aze-Chol NP induces maturation and activation of dendritic cells (DCs) through the Toll-like receptor 9 (TLR9) pathway while simultaneously delivering protein or peptide antigens to DCs in lymph nodes. The Aze-Chol NP-based nanovaccines markedly inhibited tumor growth and prolonged survival in melanoma and human papillomavirus tumor models. Moreover, combining the nanovaccine with an anti-PD-L1 antibody produced a strong synergistic effect and long-term immune memory, achieving 80% survival beyond 100 days and complete rejection of tumor cell rechallenge. Overall, our study demonstrates that this TLR9-activating carrier provides an effective and straightforward strategy for developing potent cancer vaccines.
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