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Tremelimumab: research and clinical development

The immune checkpoint therapy is a relatively recent strategy that aims to tweak the immune system to effectively attack cancer cells. The understanding of the immune responses and their regulation at the intracellular level and the development of fully humanized monoclonal antibodies are the pillar...

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Autores principales: Comin-Anduix, Begoña, Escuin-Ordinas, Helena, Ibarrondo, Francisco Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4809326/
https://www.ncbi.nlm.nih.gov/pubmed/27042127
http://dx.doi.org/10.2147/OTT.S65802
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author Comin-Anduix, Begoña
Escuin-Ordinas, Helena
Ibarrondo, Francisco Javier
author_facet Comin-Anduix, Begoña
Escuin-Ordinas, Helena
Ibarrondo, Francisco Javier
author_sort Comin-Anduix, Begoña
collection PubMed
description The immune checkpoint therapy is a relatively recent strategy that aims to tweak the immune system to effectively attack cancer cells. The understanding of the immune responses and their regulation at the intracellular level and the development of fully humanized monoclonal antibodies are the pillars of an approach that could elicit durable clinical responses and even remission in some patients with cancer. Most of the immune checkpoints that regulate the T-cell responses (activation and inhibition) operate through proteins present on the cytoplasmic membrane of the immune cells. Therefore, specific antibodies capable of blocking the inhibitory signals should lead to unrestrained immune responses that supersede the inhibitory mechanisms, which are naturally present in the tumor microenviroment. The best-known and most successful targets for immune checkpoint therapy are the cytotoxic T-lymphocyte antigen-4 and programmed cell death-1 coreceptors. Tremelimumab (CP-675,206) is a fully humanized monoclonal antibody specific for cytotoxic T-lymphocyte antigen-4, which has been successfully used to treat patients with metastatic melanoma and some other cancers. Although still a work in progress, the use of tremelimumab as an immune checkpoint therapeutic agent is a promising approach alone or in combination with other anticancer drugs. Here, we review the use of this antibody in a number of clinical trials against solid tumors.
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spelling pubmed-48093262016-04-01 Tremelimumab: research and clinical development Comin-Anduix, Begoña Escuin-Ordinas, Helena Ibarrondo, Francisco Javier Onco Targets Ther Review The immune checkpoint therapy is a relatively recent strategy that aims to tweak the immune system to effectively attack cancer cells. The understanding of the immune responses and their regulation at the intracellular level and the development of fully humanized monoclonal antibodies are the pillars of an approach that could elicit durable clinical responses and even remission in some patients with cancer. Most of the immune checkpoints that regulate the T-cell responses (activation and inhibition) operate through proteins present on the cytoplasmic membrane of the immune cells. Therefore, specific antibodies capable of blocking the inhibitory signals should lead to unrestrained immune responses that supersede the inhibitory mechanisms, which are naturally present in the tumor microenviroment. The best-known and most successful targets for immune checkpoint therapy are the cytotoxic T-lymphocyte antigen-4 and programmed cell death-1 coreceptors. Tremelimumab (CP-675,206) is a fully humanized monoclonal antibody specific for cytotoxic T-lymphocyte antigen-4, which has been successfully used to treat patients with metastatic melanoma and some other cancers. Although still a work in progress, the use of tremelimumab as an immune checkpoint therapeutic agent is a promising approach alone or in combination with other anticancer drugs. Here, we review the use of this antibody in a number of clinical trials against solid tumors. Dove Medical Press 2016-03-23 /pmc/articles/PMC4809326/ /pubmed/27042127 http://dx.doi.org/10.2147/OTT.S65802 Text en © 2016 Comin-Anduix et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Comin-Anduix, Begoña
Escuin-Ordinas, Helena
Ibarrondo, Francisco Javier
Tremelimumab: research and clinical development
title Tremelimumab: research and clinical development
title_full Tremelimumab: research and clinical development
title_fullStr Tremelimumab: research and clinical development
title_full_unstemmed Tremelimumab: research and clinical development
title_short Tremelimumab: research and clinical development
title_sort tremelimumab: research and clinical development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4809326/
https://www.ncbi.nlm.nih.gov/pubmed/27042127
http://dx.doi.org/10.2147/OTT.S65802
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