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Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies
Engineered T cells are at the leading edge of clinical cell therapy. T cell therapies have had a remarkable impact on patient care for a subset of hematological malignancies. This foundation has motivated the development of off-the-shelf engineered cell therapies for a broad range of devastating ind...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624212/ https://www.ncbi.nlm.nih.gov/pubmed/37928777 http://dx.doi.org/10.1089/genbio.2023.0008 |
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author | Michaels, Yale S. Durland, Lauren J. Zandstra, Peter W. |
author_facet | Michaels, Yale S. Durland, Lauren J. Zandstra, Peter W. |
author_sort | Michaels, Yale S. |
collection | PubMed |
description | Engineered T cells are at the leading edge of clinical cell therapy. T cell therapies have had a remarkable impact on patient care for a subset of hematological malignancies. This foundation has motivated the development of off-the-shelf engineered cell therapies for a broad range of devastating indications. Achieving this vision will require cost-effective manufacturing of precision cell products capable of addressing multiple process and clinical-design challenges. Pluripotent stem cell (PSC)-derived engineered T cells are emerging as a solution of choice. To unleash the full potential of PSC-derived T cell therapies, the field will require technologies capable of robustly orchestrating the complex series of time- and dose-dependent signaling events needed to recreate functional T cell development in the laboratory. In this article, we review the current state of allogenic T cell therapies, focusing on strategies to generate engineered lymphoid cells from PSCs. We highlight exciting recent progress in this field and outline timely opportunities for advancement with an emphasis on niche engineering and synthetic biology. |
format | Online Article Text |
id | pubmed-10624212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-106242122023-11-04 Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies Michaels, Yale S. Durland, Lauren J. Zandstra, Peter W. GEN Biotechnol Review Engineered T cells are at the leading edge of clinical cell therapy. T cell therapies have had a remarkable impact on patient care for a subset of hematological malignancies. This foundation has motivated the development of off-the-shelf engineered cell therapies for a broad range of devastating indications. Achieving this vision will require cost-effective manufacturing of precision cell products capable of addressing multiple process and clinical-design challenges. Pluripotent stem cell (PSC)-derived engineered T cells are emerging as a solution of choice. To unleash the full potential of PSC-derived T cell therapies, the field will require technologies capable of robustly orchestrating the complex series of time- and dose-dependent signaling events needed to recreate functional T cell development in the laboratory. In this article, we review the current state of allogenic T cell therapies, focusing on strategies to generate engineered lymphoid cells from PSCs. We highlight exciting recent progress in this field and outline timely opportunities for advancement with an emphasis on niche engineering and synthetic biology. Mary Ann Liebert, Inc., publishers 2023-04-01 2023-04-18 /pmc/articles/PMC10624212/ /pubmed/37928777 http://dx.doi.org/10.1089/genbio.2023.0008 Text en © Yale S. Michaels et al. 2023; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Michaels, Yale S. Durland, Lauren J. Zandstra, Peter W. Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title | Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title_full | Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title_fullStr | Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title_full_unstemmed | Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title_short | Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies |
title_sort | engineering t cell development for the next generation of stem cell-derived immunotherapies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624212/ https://www.ncbi.nlm.nih.gov/pubmed/37928777 http://dx.doi.org/10.1089/genbio.2023.0008 |
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