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Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy
Gamma delta (γδ) T cells are the all-rounders of our immune-system with their major histocompatibility complex-unrestricted cytotoxicity, capacity to secrete immunosti-mulatory cytokines and ability to promote the generation of tumor antigen-specific CD8(+) and CD4(+) T cell responses. Dendritic cel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570126/ https://www.ncbi.nlm.nih.gov/pubmed/26405575 http://dx.doi.org/10.1080/2162402X.2015.1021538 |
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author | Van Acker, Heleen H Anguille, Sébastien Van Tendeloo, Viggo F Lion, Eva |
author_facet | Van Acker, Heleen H Anguille, Sébastien Van Tendeloo, Viggo F Lion, Eva |
author_sort | Van Acker, Heleen H |
collection | PubMed |
description | Gamma delta (γδ) T cells are the all-rounders of our immune-system with their major histocompatibility complex-unrestricted cytotoxicity, capacity to secrete immunosti-mulatory cytokines and ability to promote the generation of tumor antigen-specific CD8(+) and CD4(+) T cell responses. Dendritic cell (DC)-based vaccine therapy has the prospective to harness these unique features of the γδ T cells in the fight against cancer. In this review, we will discuss our current knowledge on DC-mediated γδ T cell activation and related opportunities for tumor immunologists. |
format | Online Article Text |
id | pubmed-4570126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-45701262016-02-03 Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy Van Acker, Heleen H Anguille, Sébastien Van Tendeloo, Viggo F Lion, Eva Oncoimmunology Review Gamma delta (γδ) T cells are the all-rounders of our immune-system with their major histocompatibility complex-unrestricted cytotoxicity, capacity to secrete immunosti-mulatory cytokines and ability to promote the generation of tumor antigen-specific CD8(+) and CD4(+) T cell responses. Dendritic cell (DC)-based vaccine therapy has the prospective to harness these unique features of the γδ T cells in the fight against cancer. In this review, we will discuss our current knowledge on DC-mediated γδ T cell activation and related opportunities for tumor immunologists. Taylor & Francis 2015-04-01 /pmc/articles/PMC4570126/ /pubmed/26405575 http://dx.doi.org/10.1080/2162402X.2015.1021538 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Review Van Acker, Heleen H Anguille, Sébastien Van Tendeloo, Viggo F Lion, Eva Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title | Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title_full | Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title_fullStr | Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title_full_unstemmed | Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title_short | Empowering gamma delta T cells with antitumor immunity by dendritic cell-based immunotherapy |
title_sort | empowering gamma delta t cells with antitumor immunity by dendritic cell-based immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570126/ https://www.ncbi.nlm.nih.gov/pubmed/26405575 http://dx.doi.org/10.1080/2162402X.2015.1021538 |
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