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Engineering CAR-T Cells for Improved Function Against Solid Tumors
Genetic engineering T cells to create clinically applied chimeric antigen receptor (CAR) T cells has led to improved patient outcomes for some forms of hematopoietic malignancies. While this has inspired the biomedical community to develop similar strategies to treat solid tumor patients, challenges...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217729/ https://www.ncbi.nlm.nih.gov/pubmed/30420856 http://dx.doi.org/10.3389/fimmu.2018.02493 |
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author | Morgan, Michael A. Schambach, Axel |
author_facet | Morgan, Michael A. Schambach, Axel |
author_sort | Morgan, Michael A. |
collection | PubMed |
description | Genetic engineering T cells to create clinically applied chimeric antigen receptor (CAR) T cells has led to improved patient outcomes for some forms of hematopoietic malignancies. While this has inspired the biomedical community to develop similar strategies to treat solid tumor patients, challenges such as the immunosuppressive character of the tumor microenvironment, CAR-T cell persistence and trafficking to the tumor seem to limit CAR-T cell efficacy in solid cancers. This review provides an overview of mechanisms that tumors exploit to evade eradication by CAR-T cells as well as emerging approaches that incorporate genetic engineering technologies to improve CAR-T cell activity against solid tumors. |
format | Online Article Text |
id | pubmed-6217729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62177292018-11-12 Engineering CAR-T Cells for Improved Function Against Solid Tumors Morgan, Michael A. Schambach, Axel Front Immunol Immunology Genetic engineering T cells to create clinically applied chimeric antigen receptor (CAR) T cells has led to improved patient outcomes for some forms of hematopoietic malignancies. While this has inspired the biomedical community to develop similar strategies to treat solid tumor patients, challenges such as the immunosuppressive character of the tumor microenvironment, CAR-T cell persistence and trafficking to the tumor seem to limit CAR-T cell efficacy in solid cancers. This review provides an overview of mechanisms that tumors exploit to evade eradication by CAR-T cells as well as emerging approaches that incorporate genetic engineering technologies to improve CAR-T cell activity against solid tumors. Frontiers Media S.A. 2018-10-29 /pmc/articles/PMC6217729/ /pubmed/30420856 http://dx.doi.org/10.3389/fimmu.2018.02493 Text en Copyright © 2018 Morgan and Schambach. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Morgan, Michael A. Schambach, Axel Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title | Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title_full | Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title_fullStr | Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title_full_unstemmed | Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title_short | Engineering CAR-T Cells for Improved Function Against Solid Tumors |
title_sort | engineering car-t cells for improved function against solid tumors |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217729/ https://www.ncbi.nlm.nih.gov/pubmed/30420856 http://dx.doi.org/10.3389/fimmu.2018.02493 |
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