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Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment

There has been enormous progress this past decade in the understanding of the biology of dendritic cells (DCs) along with increasing attention for the development of novel dendritic cell (DC)-based cancer therapies. However, the clinical impact of DC-based vaccines remains to be established. This li...

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Detalles Bibliográficos
Autores principales: Gallois, Anne, Bhardwaj, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857536/
https://www.ncbi.nlm.nih.gov/pubmed/24339825
http://dx.doi.org/10.3389/fimmu.2013.00436
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author Gallois, Anne
Bhardwaj, Nina
author_facet Gallois, Anne
Bhardwaj, Nina
author_sort Gallois, Anne
collection PubMed
description There has been enormous progress this past decade in the understanding of the biology of dendritic cells (DCs) along with increasing attention for the development of novel dendritic cell (DC)-based cancer therapies. However, the clinical impact of DC-based vaccines remains to be established. This limited success could be explained by suboptimal conditions for generating potent immunostimulatory DCs as well as immune suppression mediated by the tumor microenvironment (TME). Therefore, strategies that optimize the potency of DC vaccines along with newly described therapies that target the TME in order to overcome immune dysfunction may provide durable tumor-specific immunity. These novel interventions hold the most promise for successful cancer immunotherapies.
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spelling pubmed-38575362013-12-11 Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment Gallois, Anne Bhardwaj, Nina Front Immunol Immunology There has been enormous progress this past decade in the understanding of the biology of dendritic cells (DCs) along with increasing attention for the development of novel dendritic cell (DC)-based cancer therapies. However, the clinical impact of DC-based vaccines remains to be established. This limited success could be explained by suboptimal conditions for generating potent immunostimulatory DCs as well as immune suppression mediated by the tumor microenvironment (TME). Therefore, strategies that optimize the potency of DC vaccines along with newly described therapies that target the TME in order to overcome immune dysfunction may provide durable tumor-specific immunity. These novel interventions hold the most promise for successful cancer immunotherapies. Frontiers Media S.A. 2013-12-10 /pmc/articles/PMC3857536/ /pubmed/24339825 http://dx.doi.org/10.3389/fimmu.2013.00436 Text en Copyright © 2013 Gallois and Bhardwaj. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Gallois, Anne
Bhardwaj, Nina
Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title_full Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title_fullStr Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title_full_unstemmed Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title_short Dendritic Cell-Targeted Approaches to Modulate Immune Dysfunction in the Tumor Microenvironment
title_sort dendritic cell-targeted approaches to modulate immune dysfunction in the tumor microenvironment
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857536/
https://www.ncbi.nlm.nih.gov/pubmed/24339825
http://dx.doi.org/10.3389/fimmu.2013.00436
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