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Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy

The approval of two chimeric antigen receptor-modified T cell types by the US Food and Drug Administration (FDA) for the treatment of hematologic malignancies is a milestone in immunotherapy; however, the application of CAR-T cells has been limited by antigen escape and on-target, off-tumor toxiciti...

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Detalles Bibliográficos
Autores principales: Han, Xiao, Wang, Yao, Wei, Jianshu, Han, Weidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884912/
https://www.ncbi.nlm.nih.gov/pubmed/31783889
http://dx.doi.org/10.1186/s13045-019-0813-7
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author Han, Xiao
Wang, Yao
Wei, Jianshu
Han, Weidong
author_facet Han, Xiao
Wang, Yao
Wei, Jianshu
Han, Weidong
author_sort Han, Xiao
collection PubMed
description The approval of two chimeric antigen receptor-modified T cell types by the US Food and Drug Administration (FDA) for the treatment of hematologic malignancies is a milestone in immunotherapy; however, the application of CAR-T cells has been limited by antigen escape and on-target, off-tumor toxicities. Therefore, it may be a potentially effective strategy to select appropriate targets and to combine multi-antigen-targeted CAR-T cells with “OR”, “AND” and “NOT” Boolean logic gates. We summarize the current limitations of CAR-T cells as well as the efficacy and safety of logic-gated CAR-T cells in antitumor therapy. This review will help to explore more optimized strategies to expand the CAR-T cell therapeutic window.
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spelling pubmed-68849122019-12-03 Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy Han, Xiao Wang, Yao Wei, Jianshu Han, Weidong J Hematol Oncol Review The approval of two chimeric antigen receptor-modified T cell types by the US Food and Drug Administration (FDA) for the treatment of hematologic malignancies is a milestone in immunotherapy; however, the application of CAR-T cells has been limited by antigen escape and on-target, off-tumor toxicities. Therefore, it may be a potentially effective strategy to select appropriate targets and to combine multi-antigen-targeted CAR-T cells with “OR”, “AND” and “NOT” Boolean logic gates. We summarize the current limitations of CAR-T cells as well as the efficacy and safety of logic-gated CAR-T cells in antitumor therapy. This review will help to explore more optimized strategies to expand the CAR-T cell therapeutic window. BioMed Central 2019-11-29 /pmc/articles/PMC6884912/ /pubmed/31783889 http://dx.doi.org/10.1186/s13045-019-0813-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Han, Xiao
Wang, Yao
Wei, Jianshu
Han, Weidong
Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title_full Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title_fullStr Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title_full_unstemmed Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title_short Multi-antigen-targeted chimeric antigen receptor T cells for cancer therapy
title_sort multi-antigen-targeted chimeric antigen receptor t cells for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884912/
https://www.ncbi.nlm.nih.gov/pubmed/31783889
http://dx.doi.org/10.1186/s13045-019-0813-7
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