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Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors

Adoptive cell transfer (ACT) is an emerging anticancer therapy that has shown promise in various malignancies. Redirecting antigen specificity by genetically engineering T cells to stably express receptors has become an effective variant of ACT. A novel extension of this approach is to utilize engin...

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Detalles Bibliográficos
Autores principales: Tsai, Alexander K., Davila, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910704/
https://www.ncbi.nlm.nih.gov/pubmed/27467930
http://dx.doi.org/10.1080/2162402X.2015.1122158
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author Tsai, Alexander K.
Davila, Eduardo
author_facet Tsai, Alexander K.
Davila, Eduardo
author_sort Tsai, Alexander K.
collection PubMed
description Adoptive cell transfer (ACT) is an emerging anticancer therapy that has shown promise in various malignancies. Redirecting antigen specificity by genetically engineering T cells to stably express receptors has become an effective variant of ACT. A novel extension of this approach is to utilize engineered T cells to produce and deliver anticancer therapeutics that enhance cytotoxic T cell function and simultaneously inhibit immunosuppressive processes. Here, we review the potential of using T cells as therapeutic-secreting vehicles for immunotherapies and present theoretical and established arguments in support of further development of this unique cell-based immunotherapy.
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spelling pubmed-49107042016-06-29 Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors Tsai, Alexander K. Davila, Eduardo Oncoimmunology Review Adoptive cell transfer (ACT) is an emerging anticancer therapy that has shown promise in various malignancies. Redirecting antigen specificity by genetically engineering T cells to stably express receptors has become an effective variant of ACT. A novel extension of this approach is to utilize engineered T cells to produce and deliver anticancer therapeutics that enhance cytotoxic T cell function and simultaneously inhibit immunosuppressive processes. Here, we review the potential of using T cells as therapeutic-secreting vehicles for immunotherapies and present theoretical and established arguments in support of further development of this unique cell-based immunotherapy. Taylor & Francis 2016-01-15 /pmc/articles/PMC4910704/ /pubmed/27467930 http://dx.doi.org/10.1080/2162402X.2015.1122158 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Review
Tsai, Alexander K.
Davila, Eduardo
Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title_full Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title_fullStr Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title_full_unstemmed Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title_short Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors
title_sort producer t cells: using genetically engineered t cells as vehicles to generate and deliver therapeutics to tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910704/
https://www.ncbi.nlm.nih.gov/pubmed/27467930
http://dx.doi.org/10.1080/2162402X.2015.1122158
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