Dendritic Cell–Derived Exosomes as Immunotherapies in the Fight against Cancer
Author(s) -
Jonathan M. Pitt,
Mélinda Charrier,
Sophie Viaud,
Fabrice André,
Benjamin Besse,
Nathalie Chaput,
Laurence Zitvogel
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1400703
Subject(s) - microvesicles , dendritic cell , cancer immunotherapy , cancer , immunotherapy , medicine , cancer research , immunology , biology , immune system , microrna , gene , genetics
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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