微泡
重编程
化学
癌症免疫疗法
细胞毒性T细胞
细胞生物学
单克隆抗体
癌细胞
免疫疗法
体外
抗体
癌症研究
细胞
免疫系统
癌症
生物
免疫学
小RNA
生物化学
遗传学
基因
作者
Qinqin Cheng,Xiaojing Shi,Menglu Han,Goar Smbatyan,Heinz‐Josef Lenz,Yong Zhang
摘要
Exosomes are naturally occurring membranous vesicles secreted by various types of cells. Given their unique and important biological and pharmacological properties, exosomes have been emerging as a promising form of nanomedicine acting via efficient delivery of endogenous and exogenous therapeutics. Here we explore a new concept of utilizing endogenously derived exosomes as artificial controllers of cellular immunity to redirect and activate cytotoxic T cells toward cancer cells for killing. This was achieved through genetically displaying two distinct types of antibodies on exosomal surface. The resulting synthetic multivalent antibodies retargeted exosomes (SMART-Exos), which express monoclonal antibodies specific for T-cell CD3 and cancer cell-associated epidermal growth factor receptor (EGFR), were shown to not only induce cross-linking of T cells and EGFR-expressing breast cancer cells but also elicit potent antitumor immunity both in vitro and in vivo. This proof-of-concept study demonstrates a novel application of exosomes in cancer immunotherapy and may provide a general and versatile approach for the development of a new class of cell-free therapy.
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