免疫疗法
肝细胞癌
医学
肿瘤微环境
癌症研究
免疫系统
免疫原性细胞死亡
体内
灯盏乙素
药理学
免疫学
生物
生物技术
作者
Linlin Li,Yifang Zou,Lingzhi Wang,Leilei Yang,Yutong Li,Anqi Liao,Zheng Chen,Zhuo Yu,Jianfeng Guo,Shulan Han
标识
DOI:10.1016/j.ijpharm.2023.123114
摘要
Hepatocellular carcinoma (HCC) causes the immunosuppressive tumor microenvironment (TME) resistant to current immunotherapy. The immunogenic apoptosis (currently termed immunogenic cell death, ICD) of cancer cells may induce the adaptive immunity against tumors, thereby providing great potential for treating HCC. In this study, we have confirmed the potential of scutellarin (SCU, a flavonoid found in Erigeron breviscapus) for triggering ICD in HCC cells. To facilitate in vivo application of SCU for HCC immunotherapy, an aminoethyl anisamide-targeted polyethylene glycol-modified poly(lactide-co-glycolide) (PLGA-PEG-AEAA) was produced to facilitate SCU delivery in this study. The resultant nanoformulation (PLGA-PEG-AEAA.SCU) remarkably promoted blood circulation and tumor delivery in the orthotopic HCC mouse model. Consequently, PLGA-PEG-AEAA.SCU reversed the immune suppressive TME and achieved the immunotherapeutic efficacy, resulting in significantly longer survival of mice, without inducing toxicity. These findings uncover the ICD potential of SCU and provide a promising strategy for HCC immunotherapy.
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