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Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer

Two decades of clinical cancer research with dendritic cell (DC)-based vaccination have proved that this type of personalized medicine is safe and has the capacity to improve survival, but monotherapy is unlikely to cure the cancer. Designed to empower the patient’s antitumor immunity, huge research...

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Autores principales: Versteven, Maarten, Van den Bergh, Johan M. J., Marcq, Elly, Smits, Evelien L. J., Van Tendeloo, Viggo F. I., Hobo, Willemijn, Lion, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863527/
https://www.ncbi.nlm.nih.gov/pubmed/29599770
http://dx.doi.org/10.3389/fimmu.2018.00394
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author Versteven, Maarten
Van den Bergh, Johan M. J.
Marcq, Elly
Smits, Evelien L. J.
Van Tendeloo, Viggo F. I.
Hobo, Willemijn
Lion, Eva
author_facet Versteven, Maarten
Van den Bergh, Johan M. J.
Marcq, Elly
Smits, Evelien L. J.
Van Tendeloo, Viggo F. I.
Hobo, Willemijn
Lion, Eva
author_sort Versteven, Maarten
collection PubMed
description Two decades of clinical cancer research with dendritic cell (DC)-based vaccination have proved that this type of personalized medicine is safe and has the capacity to improve survival, but monotherapy is unlikely to cure the cancer. Designed to empower the patient’s antitumor immunity, huge research efforts are set to improve the efficacy of next-generation DC vaccines and to find synergistic combinations with existing cancer therapies. Immune checkpoint approaches, aiming to breach immune suppression and evasion to reinforce antitumor immunity, have been a revelation in the immunotherapy field. Early success of therapeutic antibodies blocking the programmed death-1 (PD-1) pathway has sparked the development of novel inhibitors and combination therapies. Hence, merging immunoregulatory tumor-specific DC strategies with PD-1-targeted approaches is a promising path to explore. In this review, we focus on the role of PD-1-signaling in DC-mediated antitumor immunity. In the quest of exploiting the full potential of DC therapy, different strategies to leverage DC immunopotency by impeding PD-1-mediated immune regulation are discussed, including the most advanced research on targeted therapeutic antibodies, lessons learned from chemotherapy-induced immune activation, and more recent developments with soluble molecules and gene-silencing techniques. An overview of DC/PD-1 immunotherapy combinations that are currently under preclinical and clinical investigation substantiates the clinical potential of such combination strategies.
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spelling pubmed-58635272018-03-29 Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer Versteven, Maarten Van den Bergh, Johan M. J. Marcq, Elly Smits, Evelien L. J. Van Tendeloo, Viggo F. I. Hobo, Willemijn Lion, Eva Front Immunol Immunology Two decades of clinical cancer research with dendritic cell (DC)-based vaccination have proved that this type of personalized medicine is safe and has the capacity to improve survival, but monotherapy is unlikely to cure the cancer. Designed to empower the patient’s antitumor immunity, huge research efforts are set to improve the efficacy of next-generation DC vaccines and to find synergistic combinations with existing cancer therapies. Immune checkpoint approaches, aiming to breach immune suppression and evasion to reinforce antitumor immunity, have been a revelation in the immunotherapy field. Early success of therapeutic antibodies blocking the programmed death-1 (PD-1) pathway has sparked the development of novel inhibitors and combination therapies. Hence, merging immunoregulatory tumor-specific DC strategies with PD-1-targeted approaches is a promising path to explore. In this review, we focus on the role of PD-1-signaling in DC-mediated antitumor immunity. In the quest of exploiting the full potential of DC therapy, different strategies to leverage DC immunopotency by impeding PD-1-mediated immune regulation are discussed, including the most advanced research on targeted therapeutic antibodies, lessons learned from chemotherapy-induced immune activation, and more recent developments with soluble molecules and gene-silencing techniques. An overview of DC/PD-1 immunotherapy combinations that are currently under preclinical and clinical investigation substantiates the clinical potential of such combination strategies. Frontiers Media S.A. 2018-03-01 /pmc/articles/PMC5863527/ /pubmed/29599770 http://dx.doi.org/10.3389/fimmu.2018.00394 Text en Copyright © 2018 Versteven, Van den Bergh, Marcq, Smits, Van Tendeloo, Hobo and Lion. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner 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
Versteven, Maarten
Van den Bergh, Johan M. J.
Marcq, Elly
Smits, Evelien L. J.
Van Tendeloo, Viggo F. I.
Hobo, Willemijn
Lion, Eva
Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title_full Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title_fullStr Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title_full_unstemmed Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title_short Dendritic Cells and Programmed Death-1 Blockade: A Joint Venture to Combat Cancer
title_sort dendritic cells and programmed death-1 blockade: a joint venture to combat cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863527/
https://www.ncbi.nlm.nih.gov/pubmed/29599770
http://dx.doi.org/10.3389/fimmu.2018.00394
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