传出细胞增多
卵巢癌
癌症研究
微泡
转移
先天免疫系统
癌症
外体
免疫系统
医学
巨噬细胞
免疫学
生物
内科学
小RNA
基因
体外
生物化学
作者
Qian Li,Qingxu Song,Zhipeng Zhao,Lin Yang,Yufeng Cheng,Nathan Karin,Yuxia Luan
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-05-17
卷期号:17 (11): 10376-10392
被引量:25
标识
DOI:10.1021/acsnano.3c00804
摘要
Owing to the insidious onset of ovarian cancer, most patients are in the advanced stage with extensive peritoneal metastasis when they are diagnosed. Treatment of peritoneal metastasis from advanced ovarian cancer remains a significant challenge. Inspired by the massive macrophages in the peritoneal environment, here, we reported an artificial exosome-based peritoneal-localized hydrogel to domesticate peritoneal macrophages as the therapeutic target for realizing potent ovarian cancer therapy, where artificial exosomes derived from genetically sialic-acid-binding Ig-like lectin 10 (Siglec-10)-engineered M1-type macrophages were chemically designed as gelator. Upon triggering immunogenicity with X-ray radiation, our hydrogel encapsulating efferocytosis inhibitor MRX-2843 enabled a cascade regulation to orchestrate polarization, efferocytosis, and phagocytosis of peritoneal macrophages for realizing robust phagocytosis of tumor cells and powerful antigen presentation, offering a potent approach for ovarian cancer therapy via bridging the innate effector function of macrophages with their adaptive immune response. Moreover, our hydrogel is also applicable for potent treatment of inherent CD24-overexpressed triple-negative breast cancer, providing an emerging therapeutic regimen for the most lethal malignancies in women.
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