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Delivery technologies for T cell gene editing: Applications in cancer immunotherapy
While initial approaches to adoptive T cell therapy relied on the identification and expansion of rare tumour-reactive T cells, genetic engineering has transformed cancer immunotherapy by enabling the modification of primary T cells to increase their therapeutic potential. Specifically, gene editing...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099660/ https://www.ncbi.nlm.nih.gov/pubmed/33910123 http://dx.doi.org/10.1016/j.ebiom.2021.103354 |
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author | Atsavapranee, Ella S. Billingsley, Margaret M. Mitchell, Michael J. |
author_facet | Atsavapranee, Ella S. Billingsley, Margaret M. Mitchell, Michael J. |
author_sort | Atsavapranee, Ella S. |
collection | PubMed |
description | While initial approaches to adoptive T cell therapy relied on the identification and expansion of rare tumour-reactive T cells, genetic engineering has transformed cancer immunotherapy by enabling the modification of primary T cells to increase their therapeutic potential. Specifically, gene editing technologies have been utilized to create T cell populations with improved responses to antigens, lower rates of exhaustion, and potential for use in allogeneic applications. In this review, we provide an overview of T cell therapy gene editing strategies and the delivery technologies utilized to genetically engineer T cells. We also discuss recent investigations and clinical trials that have utilized gene editing to enhance the efficacy of T cells and broaden the application of cancer immunotherapies. |
format | Online Article Text |
id | pubmed-8099660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80996602021-05-13 Delivery technologies for T cell gene editing: Applications in cancer immunotherapy Atsavapranee, Ella S. Billingsley, Margaret M. Mitchell, Michael J. EBioMedicine Review While initial approaches to adoptive T cell therapy relied on the identification and expansion of rare tumour-reactive T cells, genetic engineering has transformed cancer immunotherapy by enabling the modification of primary T cells to increase their therapeutic potential. Specifically, gene editing technologies have been utilized to create T cell populations with improved responses to antigens, lower rates of exhaustion, and potential for use in allogeneic applications. In this review, we provide an overview of T cell therapy gene editing strategies and the delivery technologies utilized to genetically engineer T cells. We also discuss recent investigations and clinical trials that have utilized gene editing to enhance the efficacy of T cells and broaden the application of cancer immunotherapies. Elsevier 2021-04-25 /pmc/articles/PMC8099660/ /pubmed/33910123 http://dx.doi.org/10.1016/j.ebiom.2021.103354 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Atsavapranee, Ella S. Billingsley, Margaret M. Mitchell, Michael J. Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title | Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title_full | Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title_fullStr | Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title_full_unstemmed | Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title_short | Delivery technologies for T cell gene editing: Applications in cancer immunotherapy |
title_sort | delivery technologies for t cell gene editing: applications in cancer immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099660/ https://www.ncbi.nlm.nih.gov/pubmed/33910123 http://dx.doi.org/10.1016/j.ebiom.2021.103354 |
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