先天免疫系统
免疫学
免疫
免疫系统
医学
淋巴结
癌症研究
癌症
免疫检查点
接种疫苗
先天性淋巴细胞
封锁
佐剂
生物
模式识别受体
免疫疗法
信号转导
经典补体途径
获得性免疫系统
细胞凋亡
癌症疫苗
刺激
巨噬细胞
淋巴
CCL18型
作者
Fangmin Chen,Huijuan Zhang,Shuang Li,Siyuan Ren,Lujia Huang,Yu Guo,Yi Lai,Zhixiong Cai,Xiaolong Liu,Zhiai Xu,Haijun Yu
标识
DOI:10.1038/s41467-025-66976-2
摘要
Spatiotemporally-controllable regulation of innate immunity in lymph node remains a critical challenge to implement effective cancer vaccination. Here we report an ultrasound-activatable strategy to precisely stimulate innate immunity activation in vivo. Mechanistically, ultrasound-triggered mechanical and oxidative forces synchronously activate innate immune pathways in antigen-presenting cells via calcium ion influx and mitochondria DNA release. We next design a polypeptide sono-adjuvant (SONA) library with adjustable physicochemical properties for lymph node-targeting delivery. The top-performed SONA specifically activates robust and durable innate immune responses in lymph node upon localized ultrasound stimulation. The combination of SONA-based vaccine with ultrasound stimulation induces about 3.0-fold higher antigen-specific T cell responses than conventional adjuvant-based vaccines. Moreover, in syngeneic mouse models of orthotopic breast and liver tumors, the combination of SONA-based neoantigen vaccine with ultrasound stimulation markedly boosts immune checkpoint blockade therapy to suppress tumor growth and distant metastasis. Collectively, the polypeptide sono-adjuvant offers great promise for precise regulation of innate immunity and cancer vaccine therapy.
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