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Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy
T-cell therapy using genetically engineered T cells modified with either T cell receptor or chi-meric antigen receptor holds great promise for cancer immunotherapy. The concerns about its toxicities still remain despite recent successes in clinical trials. Temporal and spatial control of the enginee...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876919/ https://www.ncbi.nlm.nih.gov/pubmed/29283058 http://dx.doi.org/10.2174/1381612824666171227222624 |
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author | Ren, Yan-Bei Sun, Shang-Jun Han, Shuang-Yin |
author_facet | Ren, Yan-Bei Sun, Shang-Jun Han, Shuang-Yin |
author_sort | Ren, Yan-Bei |
collection | PubMed |
description | T-cell therapy using genetically engineered T cells modified with either T cell receptor or chi-meric antigen receptor holds great promise for cancer immunotherapy. The concerns about its toxicities still remain despite recent successes in clinical trials. Temporal and spatial control of the engineered therapeutic T cells may improve the safety profile of these treatment regimens. To achieve these goals, numerous approaches have been tested and utilized including the incorporation of a suicide gene, the switch-mediated activation, the combinatorial antigen recognition, etc. This review will summarize the toxicities caused by engineered T cells and novel strategies to overcome them. |
format | Online Article Text |
id | pubmed-5876919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-58769192018-04-11 Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy Ren, Yan-Bei Sun, Shang-Jun Han, Shuang-Yin Curr Pharm Des Article T-cell therapy using genetically engineered T cells modified with either T cell receptor or chi-meric antigen receptor holds great promise for cancer immunotherapy. The concerns about its toxicities still remain despite recent successes in clinical trials. Temporal and spatial control of the engineered therapeutic T cells may improve the safety profile of these treatment regimens. To achieve these goals, numerous approaches have been tested and utilized including the incorporation of a suicide gene, the switch-mediated activation, the combinatorial antigen recognition, etc. This review will summarize the toxicities caused by engineered T cells and novel strategies to overcome them. Bentham Science Publishers 2018-01 2018-01 /pmc/articles/PMC5876919/ /pubmed/29283058 http://dx.doi.org/10.2174/1381612824666171227222624 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Ren, Yan-Bei Sun, Shang-Jun Han, Shuang-Yin Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title | Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title_full | Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title_fullStr | Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title_full_unstemmed | Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title_short | Safety Strategies of Genetically Engineered T Cells in Cancer Immunotherapy |
title_sort | safety strategies of genetically engineered t cells in cancer immunotherapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876919/ https://www.ncbi.nlm.nih.gov/pubmed/29283058 http://dx.doi.org/10.2174/1381612824666171227222624 |
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