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Potentiating antitumor immunity with αGC-loaded exosomes

Anticancer immunotherapy is a promising treatment modality since it bears the potential of being highly specific, but effective clinical applications are still under development. We have recently described an exosome-based strategy for co-delivery of α-galactosylceramide and a tumor-associated antig...

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Autores principales: Gehrmann, Ulf, Hiltbrunner, Stefanie, Näslund, Tanja I, Gabrielsson, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862686/
https://www.ncbi.nlm.nih.gov/pubmed/24353911
http://dx.doi.org/10.4161/onci.26261
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author Gehrmann, Ulf
Hiltbrunner, Stefanie
Näslund, Tanja I
Gabrielsson, Susanne
author_facet Gehrmann, Ulf
Hiltbrunner, Stefanie
Näslund, Tanja I
Gabrielsson, Susanne
author_sort Gehrmann, Ulf
collection PubMed
description Anticancer immunotherapy is a promising treatment modality since it bears the potential of being highly specific, but effective clinical applications are still under development. We have recently described an exosome-based strategy for co-delivery of α-galactosylceramide and a tumor-associated antigen that synergistically potentiates tumor-specific adaptive immune responses while preventing the anergy of invariant natural killer T (iNKT) cells. We propose that the next generation of exosome-based immunotherapies should involve iNKT-cell ligands to induce a broad, amplified and sustainable antitumor immune response.
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spelling pubmed-38626862013-12-18 Potentiating antitumor immunity with αGC-loaded exosomes Gehrmann, Ulf Hiltbrunner, Stefanie Näslund, Tanja I Gabrielsson, Susanne Oncoimmunology Author's View Anticancer immunotherapy is a promising treatment modality since it bears the potential of being highly specific, but effective clinical applications are still under development. We have recently described an exosome-based strategy for co-delivery of α-galactosylceramide and a tumor-associated antigen that synergistically potentiates tumor-specific adaptive immune responses while preventing the anergy of invariant natural killer T (iNKT) cells. We propose that the next generation of exosome-based immunotherapies should involve iNKT-cell ligands to induce a broad, amplified and sustainable antitumor immune response. Landes Bioscience 2013-10-01 2013-10-10 /pmc/articles/PMC3862686/ /pubmed/24353911 http://dx.doi.org/10.4161/onci.26261 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Author's View
Gehrmann, Ulf
Hiltbrunner, Stefanie
Näslund, Tanja I
Gabrielsson, Susanne
Potentiating antitumor immunity with αGC-loaded exosomes
title Potentiating antitumor immunity with αGC-loaded exosomes
title_full Potentiating antitumor immunity with αGC-loaded exosomes
title_fullStr Potentiating antitumor immunity with αGC-loaded exosomes
title_full_unstemmed Potentiating antitumor immunity with αGC-loaded exosomes
title_short Potentiating antitumor immunity with αGC-loaded exosomes
title_sort potentiating antitumor immunity with αgc-loaded exosomes
topic Author's View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862686/
https://www.ncbi.nlm.nih.gov/pubmed/24353911
http://dx.doi.org/10.4161/onci.26261
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