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Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy

Anti-PD-1/PD-L1 antibodies are emerging as promising anticancer therapeutics. Interestingly, elevated response rates to these agents are mostly documented among patients with tumors that bear high level of somatic mutations, like melanoma or non-small cell lung carcinoma. We herein formulate the hyp...

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Detalles Bibliográficos
Autores principales: Champiat, Stéphane, Ferté, Charles, Lebel-Binay, Sophie, Eggermont, Alexander, Soria, Jean Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937193/
https://www.ncbi.nlm.nih.gov/pubmed/24605269
http://dx.doi.org/10.4161/onci.27817
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author Champiat, Stéphane
Ferté, Charles
Lebel-Binay, Sophie
Eggermont, Alexander
Soria, Jean Charles
author_facet Champiat, Stéphane
Ferté, Charles
Lebel-Binay, Sophie
Eggermont, Alexander
Soria, Jean Charles
author_sort Champiat, Stéphane
collection PubMed
description Anti-PD-1/PD-L1 antibodies are emerging as promising anticancer therapeutics. Interestingly, elevated response rates to these agents are mostly documented among patients with tumors that bear high level of somatic mutations, like melanoma or non-small cell lung carcinoma. We herein formulate the hypothesis that high levels of mutational heterogeneity in the tumor could be the key for the success of immune checkpoint-targeting therapies.
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spelling pubmed-39371932014-03-06 Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy Champiat, Stéphane Ferté, Charles Lebel-Binay, Sophie Eggermont, Alexander Soria, Jean Charles Oncoimmunology Point of View Anti-PD-1/PD-L1 antibodies are emerging as promising anticancer therapeutics. Interestingly, elevated response rates to these agents are mostly documented among patients with tumors that bear high level of somatic mutations, like melanoma or non-small cell lung carcinoma. We herein formulate the hypothesis that high levels of mutational heterogeneity in the tumor could be the key for the success of immune checkpoint-targeting therapies. Landes Bioscience 2014-01-16 /pmc/articles/PMC3937193/ /pubmed/24605269 http://dx.doi.org/10.4161/onci.27817 Text en Copyright © 2014 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 Point of View
Champiat, Stéphane
Ferté, Charles
Lebel-Binay, Sophie
Eggermont, Alexander
Soria, Jean Charles
Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title_full Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title_fullStr Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title_full_unstemmed Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title_short Exomics and immunogenics: Bridging mutational load and immune checkpoints efficacy
title_sort exomics and immunogenics: bridging mutational load and immune checkpoints efficacy
topic Point of View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937193/
https://www.ncbi.nlm.nih.gov/pubmed/24605269
http://dx.doi.org/10.4161/onci.27817
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