免疫疗法
免疫系统
癌症研究
癌症免疫疗法
先天免疫系统
癌症
免疫
免疫学
生物
医学
内科学
作者
Pei Pei,Yu Zhang,Yunchun Jiang,Wenhao Shen,Hua Chen,Yang Sai,Shouxin Zhang,Xuan Yi,Kai Yang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-07-12
卷期号:16 (7): 11325-11337
被引量:38
标识
DOI:10.1021/acsnano.2c04982
摘要
Biomaterial-based pleiotropic immune activation may effectively improve the response rate of immunotherapy and enhance the therapeutic effect of the tumor. Bacteria as a natural carrier have demonstrated great advantages in tumor targeted delivery and immune activation of the body. Herein, we construct an inactivated bacteria vector with 125I/131I labeling (125I-VNP/131I-VNP), which could retain radioiodine at the tumor site for a long time and deliver it into tumor cells and a tumor-associated macrophage (TAM), thus achieving efficient internal radioisotope therapy (IRT) of the primary tumor with good biosafety. More importantly, 131I-VNP-mediated local IRT could further stimulate robust systemic antitumor immune responses via activation of the cGAS-STING pathway of innate immunity and promotion of the maturation of DC cells for T-cell-dominated adaptive immunity. After combination with systemic checkpoint blockade therapy (αPD-L1), 131I-VNP, which induces the up-regulation of PD-L1 expression in the distant tumor, could lead to the inhibition of in situ colon cancer and protection against tumor rechallenge. Our strategy pioneers the use of an inactivated bacteria vector as a bridge to cleverly connect radiotherapy and immunotherapy and provide an enlightening idea for radio-immunotherapy mediated by pleiotropic immune activation functions of bacterial vectors.
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