免疫原性细胞死亡
免疫疗法
免疫系统
肿瘤微环境
癌症研究
癌症免疫疗法
纳米医学
CD8型
转移
细胞毒性
医学
癌症
化学
免疫学
纳米技术
材料科学
纳米颗粒
内科学
生物化学
体外
作者
Xinping Kuai,Yuefei Zhu,Zheng Yuan,Shengyu Wang,Lin Lin,Xiaodan Ye,Yiping Lu,Yu Luo,Zhiqing Pang,Daoying Geng,Bo Yin
标识
DOI:10.1016/j.apsb.2021.07.025
摘要
Tumor-targeted immunotherapy is a remarkable breakthrough, offering the inimitable advantage of specific tumoricidal effects with reduced immune-associated cytotoxicity. However, existing platforms suffer from low efficacy, inability to induce strong immunogenic cell death (ICD), and restrained capacity of transforming immune-deserted tumors into immune-cultivated ones. Here, an innovative platform, perfluorooctyl bromide (PFOB) nanoemulsions holding MnO2 nanoparticles (MBP), was developed to orchestrate cancer immunotherapy, serving as a theranostic nanoagent for MRI/CT dual-modality imaging and advanced ICD. By simultaneously depleting the GSH and eliciting the ICD effect via high-intensity focused ultrasound (HIFU) therapy, the MBP nanomedicine can regulate the tumor immune microenvironment by inducing maturation of dendritic cells (DCs) and facilitating the activation of CD8+ and CD4+ T cells. The synergistic GSH depletion and HIFU ablation also amplify the inhibition of tumor growth and lung metastasis. Together, these findings inaugurate a new strategy of tumor-targeted immunotherapy, realizing a novel therapeutics paradigm with great clinical significance.
科研通智能强力驱动
Strongly Powered by AbleSci AI