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Versatile CAR T-cells for cancer immunotherapy

Chimeric antigen receptor (CAR) T-cell therapy has been clinically proven to efficiently combat haematological malignancies. However, continuous efforts are required to increase the specificity of CAR T-cells against tumour versus normal tissues, and are essential to improve their antitumour activit...

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Detalles Bibliográficos
Autores principales: Chu, Fuliang, Cao, Jingjing, Neelalpu, Sattva S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885071/
https://www.ncbi.nlm.nih.gov/pubmed/29628798
http://dx.doi.org/10.5114/wo.2018.73892
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author Chu, Fuliang
Cao, Jingjing
Neelalpu, Sattva S
author_facet Chu, Fuliang
Cao, Jingjing
Neelalpu, Sattva S
author_sort Chu, Fuliang
collection PubMed
description Chimeric antigen receptor (CAR) T-cell therapy has been clinically proven to efficiently combat haematological malignancies. However, continuous efforts are required to increase the specificity of CAR T-cells against tumour versus normal tissues, and are essential to improve their antitumour activity in solid tumours. This review summarises the structure of major CAR designs, and strategies to overcome immunosuppressive tumour microenvironment, and reduce toxicities. Along with reviewing currently available techniques that allow the elimination of CAR T-cells after they fulfil their desired functions, using suicide genes, drug elimination strategies are also introduced. A better understanding of the strengths and pitfalls of CAR T-cell therapy will provide fundamental knowledge for the improvement of engineered T-cell therapy in the near future.
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spelling pubmed-58850712018-04-06 Versatile CAR T-cells for cancer immunotherapy Chu, Fuliang Cao, Jingjing Neelalpu, Sattva S Contemp Oncol (Pozn) Review Chimeric antigen receptor (CAR) T-cell therapy has been clinically proven to efficiently combat haematological malignancies. However, continuous efforts are required to increase the specificity of CAR T-cells against tumour versus normal tissues, and are essential to improve their antitumour activity in solid tumours. This review summarises the structure of major CAR designs, and strategies to overcome immunosuppressive tumour microenvironment, and reduce toxicities. Along with reviewing currently available techniques that allow the elimination of CAR T-cells after they fulfil their desired functions, using suicide genes, drug elimination strategies are also introduced. A better understanding of the strengths and pitfalls of CAR T-cell therapy will provide fundamental knowledge for the improvement of engineered T-cell therapy in the near future. Termedia Publishing House 2018-03-05 2018-03 /pmc/articles/PMC5885071/ /pubmed/29628798 http://dx.doi.org/10.5114/wo.2018.73892 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Review
Chu, Fuliang
Cao, Jingjing
Neelalpu, Sattva S
Versatile CAR T-cells for cancer immunotherapy
title Versatile CAR T-cells for cancer immunotherapy
title_full Versatile CAR T-cells for cancer immunotherapy
title_fullStr Versatile CAR T-cells for cancer immunotherapy
title_full_unstemmed Versatile CAR T-cells for cancer immunotherapy
title_short Versatile CAR T-cells for cancer immunotherapy
title_sort versatile car t-cells for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885071/
https://www.ncbi.nlm.nih.gov/pubmed/29628798
http://dx.doi.org/10.5114/wo.2018.73892
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