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Activation-inducible CAR expression enables precise control over engineered CAR T cell function
CAR T cell therapy is a rapidly growing area of oncological treatments having a potential of becoming standard care for multiple indications. Coincidently, CRISPR/Cas gene-editing technology is entering next-generation CAR T cell product manufacturing with the promise of more precise and more contro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241805/ https://www.ncbi.nlm.nih.gov/pubmed/37277433 http://dx.doi.org/10.1038/s42003-023-04978-w |
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author | Fraessle, Simon P. Tschulik, Claudia Effenberger, Manuel Cletiu, Vlad Gerget, Maria Schober, Kilian Busch, Dirk H. Germeroth, Lothar Stemberger, Christian Poltorak, Mateusz P. |
author_facet | Fraessle, Simon P. Tschulik, Claudia Effenberger, Manuel Cletiu, Vlad Gerget, Maria Schober, Kilian Busch, Dirk H. Germeroth, Lothar Stemberger, Christian Poltorak, Mateusz P. |
author_sort | Fraessle, Simon P. |
collection | PubMed |
description | CAR T cell therapy is a rapidly growing area of oncological treatments having a potential of becoming standard care for multiple indications. Coincidently, CRISPR/Cas gene-editing technology is entering next-generation CAR T cell product manufacturing with the promise of more precise and more controllable cell modification methodology. The intersection of these medical and molecular advancements creates an opportunity for completely new ways of designing engineered cells to help overcome current limitations of cell therapy. In this manuscript we present proof-of-concept data for an engineered feedback loop. We manufactured activation-inducible CAR T cells with the help of CRISPR-mediated targeted integration. This new type of engineered T cells expresses the CAR gene dependent on their activation status. This artifice opens new possibilities to regulate CAR T cell function both in vitro and in vivo. We believe that such a physiological control system can be a powerful addition to the currently available toolbox of next-generation CAR constructs. |
format | Online Article Text |
id | pubmed-10241805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102418052023-06-07 Activation-inducible CAR expression enables precise control over engineered CAR T cell function Fraessle, Simon P. Tschulik, Claudia Effenberger, Manuel Cletiu, Vlad Gerget, Maria Schober, Kilian Busch, Dirk H. Germeroth, Lothar Stemberger, Christian Poltorak, Mateusz P. Commun Biol Article CAR T cell therapy is a rapidly growing area of oncological treatments having a potential of becoming standard care for multiple indications. Coincidently, CRISPR/Cas gene-editing technology is entering next-generation CAR T cell product manufacturing with the promise of more precise and more controllable cell modification methodology. The intersection of these medical and molecular advancements creates an opportunity for completely new ways of designing engineered cells to help overcome current limitations of cell therapy. In this manuscript we present proof-of-concept data for an engineered feedback loop. We manufactured activation-inducible CAR T cells with the help of CRISPR-mediated targeted integration. This new type of engineered T cells expresses the CAR gene dependent on their activation status. This artifice opens new possibilities to regulate CAR T cell function both in vitro and in vivo. We believe that such a physiological control system can be a powerful addition to the currently available toolbox of next-generation CAR constructs. Nature Publishing Group UK 2023-06-05 /pmc/articles/PMC10241805/ /pubmed/37277433 http://dx.doi.org/10.1038/s42003-023-04978-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fraessle, Simon P. Tschulik, Claudia Effenberger, Manuel Cletiu, Vlad Gerget, Maria Schober, Kilian Busch, Dirk H. Germeroth, Lothar Stemberger, Christian Poltorak, Mateusz P. Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title | Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title_full | Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title_fullStr | Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title_full_unstemmed | Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title_short | Activation-inducible CAR expression enables precise control over engineered CAR T cell function |
title_sort | activation-inducible car expression enables precise control over engineered car t cell function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241805/ https://www.ncbi.nlm.nih.gov/pubmed/37277433 http://dx.doi.org/10.1038/s42003-023-04978-w |
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