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...

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Autores: Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f, Vacchelli, E. (Erika)|||/items/1db2a15b-f58b-4abf-833e-3785f69eb053, Eggermont, A.M. (Alexander M.)|||/items/d3a7f6a5-500d-4855-bde6-8fccf21aad37, Galon, J. (Jerome)|||/items/6a1adda1-b579-4f93-9a3d-5a8c7fc03939, Sautès-Fridman, C. (Catherine)|||/items/861ea7f2-0e92-4dd5-bb78-65169622fb43, Tartour, E. (Eric)|||/items/f3b1d85b-6bd5-446b-aad2-9cc79975059e, Zitvogel, L. (Laurence)|||/items/ad85ff59-7ca2-4f87-8931-a921648eb97b, Kroemer, G. (Guido)|||/items/ae5c18f3-0594-4a44-b71d-a367305f464f, Galluzzi, L. (Lorenzo)|||/items/a8408d1f-8344-4d64-82a7-a8775587ef8d
Tipo de recurso: artículo
Fecha de publicación:2013
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/120183
Acceso en línea:https://hdl.handle.net/10171/120183
Access Level:acceso abierto
Palabra clave:Adjuvants
Dendritic cells
Ipilimumab
NY-ESO-1
Survivin
TLR agonists
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repository_id_str
spelling Trial Watch: Peptide vaccines in cancer therapyAranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995fVacchelli, E. (Erika)|||/items/1db2a15b-f58b-4abf-833e-3785f69eb053Eggermont, A.M. (Alexander M.)|||/items/d3a7f6a5-500d-4855-bde6-8fccf21aad37Galon, J. (Jerome)|||/items/6a1adda1-b579-4f93-9a3d-5a8c7fc03939Sautès-Fridman, C. (Catherine)|||/items/861ea7f2-0e92-4dd5-bb78-65169622fb43Tartour, E. (Eric)|||/items/f3b1d85b-6bd5-446b-aad2-9cc79975059eZitvogel, L. (Laurence)|||/items/ad85ff59-7ca2-4f87-8931-a921648eb97bKroemer, G. (Guido)|||/items/ae5c18f3-0594-4a44-b71d-a367305f464fGalluzzi, L. (Lorenzo)|||/items/a8408d1f-8344-4d64-82a7-a8775587ef8dAdjuvantsDendritic cellsIpilimumabNY-ESO-1SurvivinTLR agonistsThroughout 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.Taylor & Francis GroupDadun. Depósito Académico Digital Universidad de Navarra20132013-01-0120132013-01-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10171/120183reponame:Dadun. Depósito Académico Digital de la Universidad de Navarrainstname:Universidad de NavarraInglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:dadun.unav.edu:10171/1201832026-06-21T12:47:57Z
dc.title.none.fl_str_mv Trial Watch: Peptide vaccines in cancer therapy
title Trial Watch: Peptide vaccines in cancer therapy
spellingShingle Trial Watch: Peptide vaccines in cancer therapy
Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f
Adjuvants
Dendritic cells
Ipilimumab
NY-ESO-1
Survivin
TLR agonists
title_short 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_sort Trial Watch: Peptide vaccines in cancer therapy
dc.creator.none.fl_str_mv Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f
Vacchelli, E. (Erika)|||/items/1db2a15b-f58b-4abf-833e-3785f69eb053
Eggermont, A.M. (Alexander M.)|||/items/d3a7f6a5-500d-4855-bde6-8fccf21aad37
Galon, J. (Jerome)|||/items/6a1adda1-b579-4f93-9a3d-5a8c7fc03939
Sautès-Fridman, C. (Catherine)|||/items/861ea7f2-0e92-4dd5-bb78-65169622fb43
Tartour, E. (Eric)|||/items/f3b1d85b-6bd5-446b-aad2-9cc79975059e
Zitvogel, L. (Laurence)|||/items/ad85ff59-7ca2-4f87-8931-a921648eb97b
Kroemer, G. (Guido)|||/items/ae5c18f3-0594-4a44-b71d-a367305f464f
Galluzzi, L. (Lorenzo)|||/items/a8408d1f-8344-4d64-82a7-a8775587ef8d
author Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f
author_facet Aranda-Vega, F. (Fernando)|||/items/967c4675-0318-4d3c-97dc-b5b09026995f
Vacchelli, E. (Erika)|||/items/1db2a15b-f58b-4abf-833e-3785f69eb053
Eggermont, A.M. (Alexander M.)|||/items/d3a7f6a5-500d-4855-bde6-8fccf21aad37
Galon, J. (Jerome)|||/items/6a1adda1-b579-4f93-9a3d-5a8c7fc03939
Sautès-Fridman, C. (Catherine)|||/items/861ea7f2-0e92-4dd5-bb78-65169622fb43
Tartour, E. (Eric)|||/items/f3b1d85b-6bd5-446b-aad2-9cc79975059e
Zitvogel, L. (Laurence)|||/items/ad85ff59-7ca2-4f87-8931-a921648eb97b
Kroemer, G. (Guido)|||/items/ae5c18f3-0594-4a44-b71d-a367305f464f
Galluzzi, L. (Lorenzo)|||/items/a8408d1f-8344-4d64-82a7-a8775587ef8d
author_role author
author2 Vacchelli, E. (Erika)|||/items/1db2a15b-f58b-4abf-833e-3785f69eb053
Eggermont, A.M. (Alexander M.)|||/items/d3a7f6a5-500d-4855-bde6-8fccf21aad37
Galon, J. (Jerome)|||/items/6a1adda1-b579-4f93-9a3d-5a8c7fc03939
Sautès-Fridman, C. (Catherine)|||/items/861ea7f2-0e92-4dd5-bb78-65169622fb43
Tartour, E. (Eric)|||/items/f3b1d85b-6bd5-446b-aad2-9cc79975059e
Zitvogel, L. (Laurence)|||/items/ad85ff59-7ca2-4f87-8931-a921648eb97b
Kroemer, G. (Guido)|||/items/ae5c18f3-0594-4a44-b71d-a367305f464f
Galluzzi, L. (Lorenzo)|||/items/a8408d1f-8344-4d64-82a7-a8775587ef8d
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Dadun. Depósito Académico Digital Universidad de Navarra
dc.subject.none.fl_str_mv Adjuvants
Dendritic cells
Ipilimumab
NY-ESO-1
Survivin
TLR agonists
topic Adjuvants
Dendritic cells
Ipilimumab
NY-ESO-1
Survivin
TLR agonists
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.
publishDate 2013
dc.date.none.fl_str_mv 2013
2013-01-01
2013
2013-01-01
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10171/120183
url https://hdl.handle.net/10171/120183
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Taylor & Francis Group
publisher.none.fl_str_mv Taylor & Francis Group
dc.source.none.fl_str_mv reponame:Dadun. Depósito Académico Digital de la Universidad de Navarra
instname:Universidad de Navarra
instname_str Universidad de Navarra
reponame_str Dadun. Depósito Académico Digital de la Universidad de Navarra
collection Dadun. Depósito Académico Digital de la Universidad de Navarra
repository.name.fl_str_mv
repository.mail.fl_str_mv
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