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Chimeric antigen receptor T cells: a novel therapy for solid tumors
The chimeric antigen receptor T (CAR-T) cell therapy is a newly developed adoptive antitumor treatment. Theoretically, CAR-T cells can specifically localize and eliminate tumor cells by interacting with the tumor-associated antigens (TAAs) expressing on tumor cell surface. Current studies demonstrat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372296/ https://www.ncbi.nlm.nih.gov/pubmed/28356156 http://dx.doi.org/10.1186/s13045-017-0444-9 |
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author | Yu, Shengnan Li, Anping Liu, Qian Li, Tengfei Yuan, Xun Han, Xinwei Wu, Kongming |
author_facet | Yu, Shengnan Li, Anping Liu, Qian Li, Tengfei Yuan, Xun Han, Xinwei Wu, Kongming |
author_sort | Yu, Shengnan |
collection | PubMed |
description | The chimeric antigen receptor T (CAR-T) cell therapy is a newly developed adoptive antitumor treatment. Theoretically, CAR-T cells can specifically localize and eliminate tumor cells by interacting with the tumor-associated antigens (TAAs) expressing on tumor cell surface. Current studies demonstrated that various TAAs could act as target antigens for CAR-T cells, for instance, the type III variant epidermal growth factor receptor (EGFRvIII) was considered as an ideal target for its aberrant expression on the cell surface of several tumor types. CAR-T cell therapy has achieved gratifying breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. The third generation of CAR-T demonstrates increased antitumor cytotoxicity and persistence through modification of CAR structure. In this review, we summarized the preclinical and clinical progress of CAR-T cells targeting EGFR, human epidermal growth factor receptor 2 (HER2), and mesothelin (MSLN), as well as the challenges for CAR-T cell therapy. |
format | Online Article Text |
id | pubmed-5372296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53722962017-03-31 Chimeric antigen receptor T cells: a novel therapy for solid tumors Yu, Shengnan Li, Anping Liu, Qian Li, Tengfei Yuan, Xun Han, Xinwei Wu, Kongming J Hematol Oncol Review The chimeric antigen receptor T (CAR-T) cell therapy is a newly developed adoptive antitumor treatment. Theoretically, CAR-T cells can specifically localize and eliminate tumor cells by interacting with the tumor-associated antigens (TAAs) expressing on tumor cell surface. Current studies demonstrated that various TAAs could act as target antigens for CAR-T cells, for instance, the type III variant epidermal growth factor receptor (EGFRvIII) was considered as an ideal target for its aberrant expression on the cell surface of several tumor types. CAR-T cell therapy has achieved gratifying breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. The third generation of CAR-T demonstrates increased antitumor cytotoxicity and persistence through modification of CAR structure. In this review, we summarized the preclinical and clinical progress of CAR-T cells targeting EGFR, human epidermal growth factor receptor 2 (HER2), and mesothelin (MSLN), as well as the challenges for CAR-T cell therapy. BioMed Central 2017-03-29 /pmc/articles/PMC5372296/ /pubmed/28356156 http://dx.doi.org/10.1186/s13045-017-0444-9 Text en © The Author(s). 2017 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 Yu, Shengnan Li, Anping Liu, Qian Li, Tengfei Yuan, Xun Han, Xinwei Wu, Kongming Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title | Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title_full | Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title_fullStr | Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title_full_unstemmed | Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title_short | Chimeric antigen receptor T cells: a novel therapy for solid tumors |
title_sort | chimeric antigen receptor t cells: a novel therapy for solid tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372296/ https://www.ncbi.nlm.nih.gov/pubmed/28356156 http://dx.doi.org/10.1186/s13045-017-0444-9 |
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