免疫疗法
免疫系统
CD47型
肿瘤微环境
癌症研究
医学
伤口愈合
癌症免疫疗法
转移
免疫增强剂
巨噬细胞
免疫学
癌症
生物
内科学
生物化学
体外
作者
Shupei Sheng,Limin Jin,Yan Zhang,Weiting Sun,Lin Mei,Dunwan Zhu,Xia Dong,Feng Lv
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-01-09
卷期号:18 (6): 4981-4992
被引量:7
标识
DOI:10.1021/acsnano.3c10862
摘要
During wound healing after cancer surgery, platelets, neutrophils, and macrophages accumulate at the wound site and induce important pathophysiological features. Utilizing these pathophysiological features, the development of targeted delivery systems for postoperative tumor immunotherapy is an important strategy. Herein, a twindrive precise delivery system of hybrid membrane combined with CD47 blocking is developed for targeted delivery and targeted regulation to induce postoperative immunotherapy. The precise delivery system consists of IR820-modified platelet-neutrophil hybrid membranes loaded with R848 nanoparticles. Based on the pathological characteristics of platelet aggregation and neutrophil tendency caused by the wound inflammatory microenvironment after tumor surgery, the twindrive delivery system could achieve targeted delivery and targeted regulation of immune drugs to tumor sites. After precise delivery guided by fluorescence imaging, R848 is targeted to reprogram M2 macrophages into M1 macrophages, stimulate dendritic cell maturation as an adjuvant, and then activate T cell immunity. R848 polarization and CD47 blockade together enhanced the phagocytosis function of macrophages, which combined with T cell-mediated cellular immune response to finally effectively inhibit postsurgical tumor recurrence, metastasis, and prolonged survival time. It develops a targeted delivery and regulatory system for cell-specific responses to the pathophysiological features of wound healing for postoperative immunotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI