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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...

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Detalles Bibliográficos
Autores principales: Pohl-Guimarães, Fernanda, Hoang-Minh, Lan B., Mitchell, Duane A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
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.
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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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