纳米医学
癌症研究
免疫疗法
免疫原性细胞死亡
转移
阿霉素
黑色素瘤
免疫系统
癌症
遗传增强
CD8型
癌症免疫疗法
医学
乳腺癌
癌细胞
化疗
免疫学
化学
材料科学
内科学
纳米技术
基因
纳米颗粒
生物化学
作者
Qingyan Zhang,Pengkai Wu,Jicheng Wu,Hao Shou,Xinliang Ming,Shuqi Wang,Ben Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-04-03
卷期号:17 (8): 7498-7510
被引量:16
标识
DOI:10.1021/acsnano.2c12600
摘要
Classical chemotherapeutic drugs may cause immunogenic cell death (ICD), followed by activating CD8+ T cells to promote cell-mediated antitumor immune responses. However, CD8+ T cells become exhausted due to tumor antigens' continuous stimulation, creating a major obstacle to effectively suppressing tumor growth and metastasis. Here, we develop an approach of chemo-gene combinational nanomedicine to bridge and reprogram chemotherapy and immunotherapy. The dually loaded nanomedicine induces ICD in tumor cells through doxorubicin and reverses the antitumor effects of exhausted CD8+ T cells through the small interfering RNA. The synergistic chemo-gene and fluorine assembly nanomedicine enriched in reactive oxygen species and acid-sensitive bonds results in enhanced cancer immunotherapy to inhibit tumor growth and the lung metastasis of breast cancer in a mouse model of breast cancer and melanoma. This study provides an efficient strategy and insights into chemoimmunological cascade therapy for combating malignant metastatic tumors.
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