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CAR models: next-generation CAR modifications for enhanced T-cell function

T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR...

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Detalles Bibliográficos
Autores principales: Abate-Daga, Daniel, Davila, Marco L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871190/
https://www.ncbi.nlm.nih.gov/pubmed/27231717
http://dx.doi.org/10.1038/mto.2016.14
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author Abate-Daga, Daniel
Davila, Marco L
author_facet Abate-Daga, Daniel
Davila, Marco L
author_sort Abate-Daga, Daniel
collection PubMed
description T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR technology to other cancers, as well as enhancing its efficacy and/or safety. The modular nature of the CAR, extracellular antigen-binding domain fused to a transmembrane domain and intracellular T-cell signaling domains, allows for optimization by replacement of the various components. These modifications are creating a whole new class of therapeutic CARs. In this review, we discuss the recent major advances in CAR design and how these modifications will impact its clinical application.
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spelling pubmed-48711902016-05-26 CAR models: next-generation CAR modifications for enhanced T-cell function Abate-Daga, Daniel Davila, Marco L Mol Ther Oncolytics Review Article T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR technology to other cancers, as well as enhancing its efficacy and/or safety. The modular nature of the CAR, extracellular antigen-binding domain fused to a transmembrane domain and intracellular T-cell signaling domains, allows for optimization by replacement of the various components. These modifications are creating a whole new class of therapeutic CARs. In this review, we discuss the recent major advances in CAR design and how these modifications will impact its clinical application. Nature Publishing Group 2016-05-18 /pmc/articles/PMC4871190/ /pubmed/27231717 http://dx.doi.org/10.1038/mto.2016.14 Text en Copyright © 2016 Official journal of the American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Review Article
Abate-Daga, Daniel
Davila, Marco L
CAR models: next-generation CAR modifications for enhanced T-cell function
title CAR models: next-generation CAR modifications for enhanced T-cell function
title_full CAR models: next-generation CAR modifications for enhanced T-cell function
title_fullStr CAR models: next-generation CAR modifications for enhanced T-cell function
title_full_unstemmed CAR models: next-generation CAR modifications for enhanced T-cell function
title_short CAR models: next-generation CAR modifications for enhanced T-cell function
title_sort car models: next-generation car modifications for enhanced t-cell function
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871190/
https://www.ncbi.nlm.nih.gov/pubmed/27231717
http://dx.doi.org/10.1038/mto.2016.14
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