细胞外小泡
树突状细胞
免疫疗法
小泡
化学
双特异性抗体
细胞生物学
微泡
细胞外
癌症研究
纳米技术
生物物理学
医学
免疫系统
免疫学
生物
材料科学
生物化学
小RNA
抗体
基因
单克隆抗体
膜
作者
Fang Xu,Dongpeng Jiang,Jialu Xu,Huaxing Dai,Qin Fan,Ziying Fei,Beilei Wang,Shouxin Zhang,Qingle Ma,Qianyu Yang,Yitong Chen,Edikan A. Ogunnaike,Jianhong Chu,Chao Wang
出处
期刊:Cell Reports
[Cell Press]
日期:2023-09-21
卷期号:42 (10): 113138-113138
被引量:10
标识
DOI:10.1016/j.celrep.2023.113138
摘要
Advances in the development of therapeutic extracellular vesicles (EVs) for cancer immunotherapy have allowed them to emerge as an alternative to cell therapy. In this proof-of-concept work, we develop bispecific EVs (BsEVs) by genetically engineering EV-producing dendritic cells (DCs) with aCD19 scFv and PD1 for targeting tumor antigens and blocking immune checkpoint proteins simultaneously. We find that these bispecific EVs (EVs-PD1-aCD19) have an impressive ability to accumulate in huCD19-expressing solid tumors following intravenous injection. In addition, EVs-PD1-aCD19 can remarkably reverse the immune landscape of the solid tumor by blocking PD-L1. Furthermore, EVs-PD1-aCD19 can also target tumor-derived EVs in circulation, which prevents the formation of a premetastatic niche in other tissues. Our technology is a demonstration of bispecific EV-based cancer immunotherapy, which may inspire treatments against various types of tumors with different surface antigens and even a patient-tailored therapy.
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