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Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors

The potential for adoptive cell immunotherapy as a treatment against cancers has been demonstrated by the remarkable response in some patients with hematological malignancies using autologous T cells endowed with chimeric antigen receptors (CARs) specific for CD19. Clinical efficacy of CAR-T cell th...

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Detalles Bibliográficos
Autores principales: Zhang, Erhao, Gu, Jieyi, Xu, Hanmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767005/
https://www.ncbi.nlm.nih.gov/pubmed/29329591
http://dx.doi.org/10.1186/s12943-018-0759-3
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author Zhang, Erhao
Gu, Jieyi
Xu, Hanmei
author_facet Zhang, Erhao
Gu, Jieyi
Xu, Hanmei
author_sort Zhang, Erhao
collection PubMed
description The potential for adoptive cell immunotherapy as a treatment against cancers has been demonstrated by the remarkable response in some patients with hematological malignancies using autologous T cells endowed with chimeric antigen receptors (CARs) specific for CD19. Clinical efficacy of CAR-T cell therapy for the treatment of solid tumors, however, is rare due to physical and biochemical factors. This review focuses on different aspects of multiple mechanisms of immunosuppression in solid tumors. We characterize the current state of CAR-modified T cell therapy and summarize the various strategies to combat the immunosuppressive microenvironment of solid tumors, with the aim of promoting T cell cytotoxicity and enhancing tumor cell eradication.
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spelling pubmed-57670052018-01-17 Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors Zhang, Erhao Gu, Jieyi Xu, Hanmei Mol Cancer Review The potential for adoptive cell immunotherapy as a treatment against cancers has been demonstrated by the remarkable response in some patients with hematological malignancies using autologous T cells endowed with chimeric antigen receptors (CARs) specific for CD19. Clinical efficacy of CAR-T cell therapy for the treatment of solid tumors, however, is rare due to physical and biochemical factors. This review focuses on different aspects of multiple mechanisms of immunosuppression in solid tumors. We characterize the current state of CAR-modified T cell therapy and summarize the various strategies to combat the immunosuppressive microenvironment of solid tumors, with the aim of promoting T cell cytotoxicity and enhancing tumor cell eradication. BioMed Central 2018-01-12 /pmc/articles/PMC5767005/ /pubmed/29329591 http://dx.doi.org/10.1186/s12943-018-0759-3 Text en © The Author(s). 2018 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
Zhang, Erhao
Gu, Jieyi
Xu, Hanmei
Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title_full Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title_fullStr Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title_full_unstemmed Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title_short Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors
title_sort prospects for chimeric antigen receptor-modified t cell therapy for solid tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767005/
https://www.ncbi.nlm.nih.gov/pubmed/29329591
http://dx.doi.org/10.1186/s12943-018-0759-3
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