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Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy

The genetic modification and characterization of T-cells with chimeric antigen receptors (CARs) allow functionally distinct T-cell subsets to recognize specific tumor cells. The incorporation of costimulatory molecules or cytokines can enable engineered T-cells to eliminate tumor cells. CARs are gen...

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Detalles Bibliográficos
Autores principales: Dai, Hanren, Wang, Yao, Lu, Xuechun, Han, Weidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948566/
https://www.ncbi.nlm.nih.gov/pubmed/26819347
http://dx.doi.org/10.1093/jnci/djv439
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author Dai, Hanren
Wang, Yao
Lu, Xuechun
Han, Weidong
author_facet Dai, Hanren
Wang, Yao
Lu, Xuechun
Han, Weidong
author_sort Dai, Hanren
collection PubMed
description The genetic modification and characterization of T-cells with chimeric antigen receptors (CARs) allow functionally distinct T-cell subsets to recognize specific tumor cells. The incorporation of costimulatory molecules or cytokines can enable engineered T-cells to eliminate tumor cells. CARs are generated by fusing the antigen-binding region of a monoclonal antibody (mAb) or other ligand to membrane-spanning and intracellular-signaling domains. They have recently shown clinical benefit in patients treated with CD19-directed autologous T-cells. Recent successes suggest that the modification of T-cells with CARs could be a powerful approach for developing safe and effective cancer therapeutics. Here, we briefly review early studies, consider strategies to improve the therapeutic potential and safety, and discuss the challenges and future prospects for CAR T-cells in cancer therapy.
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spelling pubmed-49485662016-07-20 Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy Dai, Hanren Wang, Yao Lu, Xuechun Han, Weidong J Natl Cancer Inst Review The genetic modification and characterization of T-cells with chimeric antigen receptors (CARs) allow functionally distinct T-cell subsets to recognize specific tumor cells. The incorporation of costimulatory molecules or cytokines can enable engineered T-cells to eliminate tumor cells. CARs are generated by fusing the antigen-binding region of a monoclonal antibody (mAb) or other ligand to membrane-spanning and intracellular-signaling domains. They have recently shown clinical benefit in patients treated with CD19-directed autologous T-cells. Recent successes suggest that the modification of T-cells with CARs could be a powerful approach for developing safe and effective cancer therapeutics. Here, we briefly review early studies, consider strategies to improve the therapeutic potential and safety, and discuss the challenges and future prospects for CAR T-cells in cancer therapy. Oxford University Press 2016-01-27 /pmc/articles/PMC4948566/ /pubmed/26819347 http://dx.doi.org/10.1093/jnci/djv439 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review
Dai, Hanren
Wang, Yao
Lu, Xuechun
Han, Weidong
Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title_full Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title_fullStr Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title_full_unstemmed Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title_short Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy
title_sort chimeric antigen receptors modified t-cells for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948566/
https://www.ncbi.nlm.nih.gov/pubmed/26819347
http://dx.doi.org/10.1093/jnci/djv439
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