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Design of chimeric antigen receptors with integrated controllable transient functions
The ability to control T cells engineered to permanently express chimeric antigen receptors (CARs) is a key feature to improve safety. Here, we describe the development of a new CAR architecture with an integrated switch-on system that permits to control the CAR T-cell function. This system offers t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707440/ https://www.ncbi.nlm.nih.gov/pubmed/26750734 http://dx.doi.org/10.1038/srep18950 |
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author | Juillerat, Alexandre Marechal, Alan Filhol, Jean-Marie Valton, Julien Duclert, Aymeric Poirot, Laurent Duchateau, Philippe |
author_facet | Juillerat, Alexandre Marechal, Alan Filhol, Jean-Marie Valton, Julien Duclert, Aymeric Poirot, Laurent Duchateau, Philippe |
author_sort | Juillerat, Alexandre |
collection | PubMed |
description | The ability to control T cells engineered to permanently express chimeric antigen receptors (CARs) is a key feature to improve safety. Here, we describe the development of a new CAR architecture with an integrated switch-on system that permits to control the CAR T-cell function. This system offers the advantage of a transient CAR T-cell for safety while letting open the possibility of multiple cytotoxicity cycles using a small molecule drug. |
format | Online Article Text |
id | pubmed-4707440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47074402016-01-20 Design of chimeric antigen receptors with integrated controllable transient functions Juillerat, Alexandre Marechal, Alan Filhol, Jean-Marie Valton, Julien Duclert, Aymeric Poirot, Laurent Duchateau, Philippe Sci Rep Article The ability to control T cells engineered to permanently express chimeric antigen receptors (CARs) is a key feature to improve safety. Here, we describe the development of a new CAR architecture with an integrated switch-on system that permits to control the CAR T-cell function. This system offers the advantage of a transient CAR T-cell for safety while letting open the possibility of multiple cytotoxicity cycles using a small molecule drug. Nature Publishing Group 2016-01-11 /pmc/articles/PMC4707440/ /pubmed/26750734 http://dx.doi.org/10.1038/srep18950 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/ |
spellingShingle | Article Juillerat, Alexandre Marechal, Alan Filhol, Jean-Marie Valton, Julien Duclert, Aymeric Poirot, Laurent Duchateau, Philippe Design of chimeric antigen receptors with integrated controllable transient functions |
title | Design of chimeric antigen receptors with integrated controllable transient functions |
title_full | Design of chimeric antigen receptors with integrated controllable transient functions |
title_fullStr | Design of chimeric antigen receptors with integrated controllable transient functions |
title_full_unstemmed | Design of chimeric antigen receptors with integrated controllable transient functions |
title_short | Design of chimeric antigen receptors with integrated controllable transient functions |
title_sort | design of chimeric antigen receptors with integrated controllable transient functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707440/ https://www.ncbi.nlm.nih.gov/pubmed/26750734 http://dx.doi.org/10.1038/srep18950 |
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