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RNA-electroporated T cells for cancer immunotherapy
Adoptive T cell therapy has proven effective against hematologic malignancies and demonstrated efficacy against a variety of solid tumors in preclinical studies and clinical trials. Nonetheless, antitumor responses against solid tumors remain modest, highlighting the need to enhance the effectivenes...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553534/ https://www.ncbi.nlm.nih.gov/pubmed/33101771 http://dx.doi.org/10.1080/2162402X.2020.1792625 |
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author | Pohl-Guimarães, Fernanda Hoang-Minh, Lan B. Mitchell, Duane A. |
author_facet | Pohl-Guimarães, Fernanda Hoang-Minh, Lan B. Mitchell, Duane A. |
author_sort | Pohl-Guimarães, Fernanda |
collection | PubMed |
description | Adoptive T cell therapy has proven effective against hematologic malignancies and demonstrated efficacy against a variety of solid tumors in preclinical studies and clinical trials. Nonetheless, antitumor responses against solid tumors remain modest, highlighting the need to enhance the effectiveness of this therapy. Genetic modification of T cells with RNA has been explored to enhance T-cell antigen specificity, effector function, and migration to tumor sites, thereby potentiating antitumor immunity. This review describes the rationale for RNA-electroporated T cell modifications and provides an overview of their applications in preclinical and clinical investigations for the treatment of hematologic malignancies and solid tumors. |
format | Online Article Text |
id | pubmed-7553534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75535342020-10-23 RNA-electroporated T cells for cancer immunotherapy Pohl-Guimarães, Fernanda Hoang-Minh, Lan B. Mitchell, Duane A. Oncoimmunology Review Adoptive T cell therapy has proven effective against hematologic malignancies and demonstrated efficacy against a variety of solid tumors in preclinical studies and clinical trials. Nonetheless, antitumor responses against solid tumors remain modest, highlighting the need to enhance the effectiveness of this therapy. Genetic modification of T cells with RNA has been explored to enhance T-cell antigen specificity, effector function, and migration to tumor sites, thereby potentiating antitumor immunity. This review describes the rationale for RNA-electroporated T cell modifications and provides an overview of their applications in preclinical and clinical investigations for the treatment of hematologic malignancies and solid tumors. Taylor & Francis 2020-10-07 /pmc/articles/PMC7553534/ /pubmed/33101771 http://dx.doi.org/10.1080/2162402X.2020.1792625 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Pohl-Guimarães, Fernanda Hoang-Minh, Lan B. Mitchell, Duane A. RNA-electroporated T cells for cancer immunotherapy |
title | RNA-electroporated T cells for cancer immunotherapy |
title_full | RNA-electroporated T cells for cancer immunotherapy |
title_fullStr | RNA-electroporated T cells for cancer immunotherapy |
title_full_unstemmed | RNA-electroporated T cells for cancer immunotherapy |
title_short | RNA-electroporated T cells for cancer immunotherapy |
title_sort | rna-electroporated t cells for cancer immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553534/ https://www.ncbi.nlm.nih.gov/pubmed/33101771 http://dx.doi.org/10.1080/2162402X.2020.1792625 |
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