Cargando…

Trial Watch: Peptide vaccines in cancer therapy

Throughout the past 3 decades, along with the recognition that the immune system not only influences oncogenesis and tumor progression, but also determines how established neoplastic lesions respond therapy, renovated enthusiasm has gathered around the possibility of using vaccines as anticancer age...

Descripción completa

Detalles Bibliográficos
Autores principales: Aranda, Fernando, Vacchelli, Erika, Eggermont, Alexander, Galon, Jerome, Sautès-Fridman, Catherine, Tartour, Eric, Zitvogel, Laurence, Kroemer, Guido, Galluzzi, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902120/
https://www.ncbi.nlm.nih.gov/pubmed/24498550
http://dx.doi.org/10.4161/onci.26621
_version_ 1782300949679702016
author Aranda, Fernando
Vacchelli, Erika
Eggermont, Alexander
Galon, Jerome
Sautès-Fridman, Catherine
Tartour, Eric
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
author_facet Aranda, Fernando
Vacchelli, Erika
Eggermont, Alexander
Galon, Jerome
Sautès-Fridman, Catherine
Tartour, Eric
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
author_sort Aranda, Fernando
collection PubMed
description Throughout the past 3 decades, along with the recognition that the immune system not only influences oncogenesis and tumor progression, but also determines how established neoplastic lesions respond therapy, renovated enthusiasm has gathered around the possibility of using vaccines as anticancer agents. Such an enthusiasm quickly tempered when it became clear that anticancer vaccines would have to be devised as therapeutic, rather than prophylactic, measures, and that malignant cells often fail to elicit (or actively suppress) innate and adaptive immune responses. Nonetheless, accumulating evidence indicates that a variety of anticancer vaccines, including cell-based, DNA-based, and purified component-based preparations, are capable of circumventing the poorly immunogenic and highly immunosuppressive nature of most tumors and elicit (at least under some circumstances) therapeutically relevant immune responses. Great efforts are currently being devoted to the identification of strategies that may provide anticancer vaccines with the capacity of breaking immunological tolerance and eliciting tumor-associated antigen-specific immunity in a majority of patients. In this sense, promising results have been obtained by combining anticancer vaccines with a relatively varied panels of adjuvants, including multiple immunostimulatory cytokines, Toll-like receptor agonists as well as inhibitors of immune checkpoints. One year ago, in the December issue of OncoImmunology, we discussed the biological mechanisms that underlie the antineoplastic effects of peptide-based vaccines and presented an abundant literature demonstrating the prominent clinical potential of such an approach. Here, we review the latest developments in this exciting area of research, focusing on high-profile studies that have been published during the last 13 mo and clinical trials launched in the same period to evaluate purified peptides or full-length proteins as therapeutic anticancer agents.
format Online
Article
Text
id pubmed-3902120
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Landes Bioscience
record_format MEDLINE/PubMed
spelling pubmed-39021202014-02-04 Trial Watch: Peptide vaccines in cancer therapy Aranda, Fernando Vacchelli, Erika Eggermont, Alexander Galon, Jerome Sautès-Fridman, Catherine Tartour, Eric Zitvogel, Laurence Kroemer, Guido Galluzzi, Lorenzo Oncoimmunology Review Throughout the past 3 decades, along with the recognition that the immune system not only influences oncogenesis and tumor progression, but also determines how established neoplastic lesions respond therapy, renovated enthusiasm has gathered around the possibility of using vaccines as anticancer agents. Such an enthusiasm quickly tempered when it became clear that anticancer vaccines would have to be devised as therapeutic, rather than prophylactic, measures, and that malignant cells often fail to elicit (or actively suppress) innate and adaptive immune responses. Nonetheless, accumulating evidence indicates that a variety of anticancer vaccines, including cell-based, DNA-based, and purified component-based preparations, are capable of circumventing the poorly immunogenic and highly immunosuppressive nature of most tumors and elicit (at least under some circumstances) therapeutically relevant immune responses. Great efforts are currently being devoted to the identification of strategies that may provide anticancer vaccines with the capacity of breaking immunological tolerance and eliciting tumor-associated antigen-specific immunity in a majority of patients. In this sense, promising results have been obtained by combining anticancer vaccines with a relatively varied panels of adjuvants, including multiple immunostimulatory cytokines, Toll-like receptor agonists as well as inhibitors of immune checkpoints. One year ago, in the December issue of OncoImmunology, we discussed the biological mechanisms that underlie the antineoplastic effects of peptide-based vaccines and presented an abundant literature demonstrating the prominent clinical potential of such an approach. Here, we review the latest developments in this exciting area of research, focusing on high-profile studies that have been published during the last 13 mo and clinical trials launched in the same period to evaluate purified peptides or full-length proteins as therapeutic anticancer agents. Landes Bioscience 2013-12-01 2013-11-04 /pmc/articles/PMC3902120/ /pubmed/24498550 http://dx.doi.org/10.4161/onci.26621 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 Review
Aranda, Fernando
Vacchelli, Erika
Eggermont, Alexander
Galon, Jerome
Sautès-Fridman, Catherine
Tartour, Eric
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
Trial Watch: Peptide vaccines in cancer therapy
title Trial Watch: Peptide vaccines in cancer therapy
title_full Trial Watch: Peptide vaccines in cancer therapy
title_fullStr Trial Watch: Peptide vaccines in cancer therapy
title_full_unstemmed Trial Watch: Peptide vaccines in cancer therapy
title_short Trial Watch: Peptide vaccines in cancer therapy
title_sort trial watch: peptide vaccines in cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902120/
https://www.ncbi.nlm.nih.gov/pubmed/24498550
http://dx.doi.org/10.4161/onci.26621
work_keys_str_mv AT arandafernando trialwatchpeptidevaccinesincancertherapy
AT vacchellierika trialwatchpeptidevaccinesincancertherapy
AT eggermontalexander trialwatchpeptidevaccinesincancertherapy
AT galonjerome trialwatchpeptidevaccinesincancertherapy
AT sautesfridmancatherine trialwatchpeptidevaccinesincancertherapy
AT tartoureric trialwatchpeptidevaccinesincancertherapy
AT zitvogellaurence trialwatchpeptidevaccinesincancertherapy
AT kroemerguido trialwatchpeptidevaccinesincancertherapy
AT galluzzilorenzo trialwatchpeptidevaccinesincancertherapy