Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality
Engineered T cells work as living therapeutics, but are prone to hyperreactivity and exhaustion. Here the authors improve CAR T cell antitumor responses by simultaneously targeting a CAR to TCR locus and IL-12 to PD1 locus, placing the transgenes under a naturally regulated transcriptional network w...
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Nature Portfolio
2019
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oai:doaj.org-article:981675c72a9b4f029d140df08e0be5fe2021-12-02T15:35:05ZRepurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality10.1038/s41467-019-13088-32041-1723https://doaj.org/article/981675c72a9b4f029d140df08e0be5fe2019-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-13088-3https://doaj.org/toc/2041-1723Engineered T cells work as living therapeutics, but are prone to hyperreactivity and exhaustion. Here the authors improve CAR T cell antitumor responses by simultaneously targeting a CAR to TCR locus and IL-12 to PD1 locus, placing the transgenes under a naturally regulated transcriptional network while disrupting unwanted signals.Mohit SachdevaBrian W. BusserSonal TemburniBillal JahangiriAnne-Sophie GautronAlan MaréchalAlexandre JuilleratAlan WilliamsStéphane DepilPhilippe DuchateauLaurent PoirotJulien ValtonNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-16 (2019) |
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Science Q Mohit Sachdeva Brian W. Busser Sonal Temburni Billal Jahangiri Anne-Sophie Gautron Alan Maréchal Alexandre Juillerat Alan Williams Stéphane Depil Philippe Duchateau Laurent Poirot Julien Valton Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
description |
Engineered T cells work as living therapeutics, but are prone to hyperreactivity and exhaustion. Here the authors improve CAR T cell antitumor responses by simultaneously targeting a CAR to TCR locus and IL-12 to PD1 locus, placing the transgenes under a naturally regulated transcriptional network while disrupting unwanted signals. |
format |
article |
author |
Mohit Sachdeva Brian W. Busser Sonal Temburni Billal Jahangiri Anne-Sophie Gautron Alan Maréchal Alexandre Juillerat Alan Williams Stéphane Depil Philippe Duchateau Laurent Poirot Julien Valton |
author_facet |
Mohit Sachdeva Brian W. Busser Sonal Temburni Billal Jahangiri Anne-Sophie Gautron Alan Maréchal Alexandre Juillerat Alan Williams Stéphane Depil Philippe Duchateau Laurent Poirot Julien Valton |
author_sort |
Mohit Sachdeva |
title |
Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
title_short |
Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
title_full |
Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
title_fullStr |
Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
title_full_unstemmed |
Repurposing endogenous immune pathways to tailor and control chimeric antigen receptor T cell functionality |
title_sort |
repurposing endogenous immune pathways to tailor and control chimeric antigen receptor t cell functionality |
publisher |
Nature Portfolio |
publishDate |
2019 |
url |
https://doaj.org/article/981675c72a9b4f029d140df08e0be5fe |
work_keys_str_mv |
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