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Engineering Next-Generation CAR-T Cells for Better Toxicity Management

Immunoadoptive therapy with genetically modified T lymphocytes expressing chimeric antigen receptors (CARs) has revolutionized the treatment of patients with hematologic cancers. Although clinical outcomes in B-cell malignancies are impressive, researchers are seeking to enhance the activity, persis...

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Autores principales: Andrea, Alain E., Chiron, Andrada, Bessoles, Stéphanie, Hacein-Bey-Abina, Salima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696189/
https://www.ncbi.nlm.nih.gov/pubmed/33207607
http://dx.doi.org/10.3390/ijms21228620
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author Andrea, Alain E.
Chiron, Andrada
Bessoles, Stéphanie
Hacein-Bey-Abina, Salima
author_facet Andrea, Alain E.
Chiron, Andrada
Bessoles, Stéphanie
Hacein-Bey-Abina, Salima
author_sort Andrea, Alain E.
collection PubMed
description Immunoadoptive therapy with genetically modified T lymphocytes expressing chimeric antigen receptors (CARs) has revolutionized the treatment of patients with hematologic cancers. Although clinical outcomes in B-cell malignancies are impressive, researchers are seeking to enhance the activity, persistence, and also safety of CAR-T cell therapy—notably with a view to mitigating potentially serious or even life-threatening adverse events like on-target/off-tumor toxicity and (in particular) cytokine release syndrome. A variety of safety strategies have been developed by replacing or adding various components (such as OFF- and ON-switch CARs) or by combining multi-antigen-targeting OR-, AND- and NOT-gate CAR-T cells. This research has laid the foundations for a whole new generation of therapeutic CAR-T cells. Here, we review the most promising CAR-T cell safety strategies and the corresponding preclinical and clinical studies.
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spelling pubmed-76961892020-11-29 Engineering Next-Generation CAR-T Cells for Better Toxicity Management Andrea, Alain E. Chiron, Andrada Bessoles, Stéphanie Hacein-Bey-Abina, Salima Int J Mol Sci Review Immunoadoptive therapy with genetically modified T lymphocytes expressing chimeric antigen receptors (CARs) has revolutionized the treatment of patients with hematologic cancers. Although clinical outcomes in B-cell malignancies are impressive, researchers are seeking to enhance the activity, persistence, and also safety of CAR-T cell therapy—notably with a view to mitigating potentially serious or even life-threatening adverse events like on-target/off-tumor toxicity and (in particular) cytokine release syndrome. A variety of safety strategies have been developed by replacing or adding various components (such as OFF- and ON-switch CARs) or by combining multi-antigen-targeting OR-, AND- and NOT-gate CAR-T cells. This research has laid the foundations for a whole new generation of therapeutic CAR-T cells. Here, we review the most promising CAR-T cell safety strategies and the corresponding preclinical and clinical studies. MDPI 2020-11-16 /pmc/articles/PMC7696189/ /pubmed/33207607 http://dx.doi.org/10.3390/ijms21228620 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Andrea, Alain E.
Chiron, Andrada
Bessoles, Stéphanie
Hacein-Bey-Abina, Salima
Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title_full Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title_fullStr Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title_full_unstemmed Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title_short Engineering Next-Generation CAR-T Cells for Better Toxicity Management
title_sort engineering next-generation car-t cells for better toxicity management
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696189/
https://www.ncbi.nlm.nih.gov/pubmed/33207607
http://dx.doi.org/10.3390/ijms21228620
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