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Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects

Chimeric antigen receptors (CARs) are recombinant receptors that combine the specificity of an antigen-specific antibody with the T-cell’s activating functions. Initial clinical trials of genetically engineered CAR T cells have significantly raised the profile of T cell therapy, and great efforts ha...

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Detalles Bibliográficos
Autores principales: Shi, Huan, Sun, Meili, Liu, Lin, Wang, Zhehai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177696/
https://www.ncbi.nlm.nih.gov/pubmed/25241075
http://dx.doi.org/10.1186/1476-4598-13-219
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author Shi, Huan
Sun, Meili
Liu, Lin
Wang, Zhehai
author_facet Shi, Huan
Sun, Meili
Liu, Lin
Wang, Zhehai
author_sort Shi, Huan
collection PubMed
description Chimeric antigen receptors (CARs) are recombinant receptors that combine the specificity of an antigen-specific antibody with the T-cell’s activating functions. Initial clinical trials of genetically engineered CAR T cells have significantly raised the profile of T cell therapy, and great efforts have been made to improve this approach. In this review, we provide a structural overview of the development of CAR technology and highlight areas that require further refinement. We also discuss critical issues related to CAR therapy, including the optimization of CAR T cells, the route of administration, CAR toxicity and the blocking of inhibitory molecules.
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spelling pubmed-41776962014-09-29 Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects Shi, Huan Sun, Meili Liu, Lin Wang, Zhehai Mol Cancer Review Chimeric antigen receptors (CARs) are recombinant receptors that combine the specificity of an antigen-specific antibody with the T-cell’s activating functions. Initial clinical trials of genetically engineered CAR T cells have significantly raised the profile of T cell therapy, and great efforts have been made to improve this approach. In this review, we provide a structural overview of the development of CAR technology and highlight areas that require further refinement. We also discuss critical issues related to CAR therapy, including the optimization of CAR T cells, the route of administration, CAR toxicity and the blocking of inhibitory molecules. BioMed Central 2014-09-21 /pmc/articles/PMC4177696/ /pubmed/25241075 http://dx.doi.org/10.1186/1476-4598-13-219 Text en © Shi et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Shi, Huan
Sun, Meili
Liu, Lin
Wang, Zhehai
Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title_full Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title_fullStr Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title_full_unstemmed Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title_short Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
title_sort chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177696/
https://www.ncbi.nlm.nih.gov/pubmed/25241075
http://dx.doi.org/10.1186/1476-4598-13-219
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