微泡
树突状细胞
癌症免疫疗法
癌症
免疫疗法
医学
癌症研究
免疫学
生物
免疫系统
小RNA
内科学
基因
遗传学
作者
Jonathan M. Pitt,Mélinda Charrier,Sophie Viaud,Fabrice André,Benjamin Besse,Nathalie Chaput,Laurence Zitvogel
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2014-07-21
卷期号:193 (3): 1006-1011
被引量:281
标识
DOI:10.4049/jimmunol.1400703
摘要
Exosomes are nanometric membrane vesicles of late endosomal origin released by most, if not all, cell types as a means of sophisticated intercellular communication. A multitude of studies showed how exosomes can mediate and regulate immune responses against tumors. Dendritic cell-derived exosomes (Dex) have received much attention as immunotherapeutic anticancer agents since the discovery that they harbor functional MHC-peptide complexes, in addition to various other immune-stimulating components, that together facilitate immune cell-dependent tumor rejection. The therapeutic potential of Dex has been substantiated with their development and clinical testing in the treatment of cancer. This review focuses on mechanisms by which Dex interact with and influence immune cells and describes how they can be engineered to promote their immunogenic capacity as novel and dynamic anticancer agents.
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