免疫系统
免疫疗法
癌症免疫疗法
癌细胞
抗原呈递
树突状细胞
癌症研究
抗原
癌症
细胞
免疫原性细胞死亡
交叉展示
材料科学
T细胞
生物
免疫学
生物化学
遗传学
作者
Zhixiang Lu,Shuang Bai,Yonghe Jiang,Shuaiying Wu,Dazhuang Xu,Jianzhong Zhang,Xuqi Peng,Hongrui Zhang,Yesi Shi,Gang Liu
出处
期刊:Small
[Wiley]
日期:2022-09-23
卷期号:18 (44)
被引量:29
标识
DOI:10.1002/smll.202203952
摘要
Despite recent advancements of sonodynamic therapy (SDT) in cancer immunotherapy, challenges have yet to be surmounted to further boost its immunotherapeutic efficacy due to the low-level tumor antigens presentation of dendritic cells (DCs). Cell membrane camouflaged-nanoparticles can integrate the neoantigens of the cancer cell membrane with the multifunctionalities of synthetic nanocores. Herein, sono-responsive nanoparticles coated with DC-targeted antibody chimeric cancer cell membrane are investigated for multimodal therapy. The nanometal organic frameworks (MOFs) that respond to ultrasound are loaded successfully inside the vesicles displaying an anti-DEC205 antibody. The anti-DEC205 chimeric vesicles can directly target and activate DCs, promote tumor antigens cross-presentation, and then produce a cascade amplified T-cell immune response. Upon deep tissue-penetrating sonication, [email protected] generates large amounts of reactive oxygen species that directly kill cancer cells, further initiating an anti-cancer T cell immune response. Such synergistic sono-immunotherapies effectually inhibit tumor growth and induce strong systemic and long-term immune memory against cancer recurrence and distant metastasis. The authors findings provide DCs and tumor cells of a dual active-targeting cell membrane-coated sono-immunotherapeutic nanoplatform for cancer therapy.
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