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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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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. |
format | Online Article Text |
id | pubmed-4809326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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