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Genetic Engineering and Manufacturing of Hematopoietic Stem Cells

The marketing approval of genetically engineered hematopoietic stem cells (HSCs) as the first-line therapy for the treatment of severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID) is a tribute to the substantial progress that has been made regarding HSC engineering in t...

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Detalles Bibliográficos
Autores principales: Wang, Xiuyan, Rivière, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415326/
https://www.ncbi.nlm.nih.gov/pubmed/28480310
http://dx.doi.org/10.1016/j.omtm.2017.03.003
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author Wang, Xiuyan
Rivière, Isabelle
author_facet Wang, Xiuyan
Rivière, Isabelle
author_sort Wang, Xiuyan
collection PubMed
description The marketing approval of genetically engineered hematopoietic stem cells (HSCs) as the first-line therapy for the treatment of severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID) is a tribute to the substantial progress that has been made regarding HSC engineering in the past decade. Reproducible manufacturing of high-quality, clinical-grade, genetically engineered HSCs is the foundation for broadening the application of this technology. Herein, the current state-of-the-art manufacturing platforms to genetically engineer HSCs as well as the challenges pertaining to production standardization and product characterization are addressed in the context of primary immunodeficiency diseases (PIDs) and other monogenic disorders.
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spelling pubmed-54153262017-05-05 Genetic Engineering and Manufacturing of Hematopoietic Stem Cells Wang, Xiuyan Rivière, Isabelle Mol Ther Methods Clin Dev Review The marketing approval of genetically engineered hematopoietic stem cells (HSCs) as the first-line therapy for the treatment of severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID) is a tribute to the substantial progress that has been made regarding HSC engineering in the past decade. Reproducible manufacturing of high-quality, clinical-grade, genetically engineered HSCs is the foundation for broadening the application of this technology. Herein, the current state-of-the-art manufacturing platforms to genetically engineer HSCs as well as the challenges pertaining to production standardization and product characterization are addressed in the context of primary immunodeficiency diseases (PIDs) and other monogenic disorders. American Society of Gene & Cell Therapy 2017-03-18 /pmc/articles/PMC5415326/ /pubmed/28480310 http://dx.doi.org/10.1016/j.omtm.2017.03.003 Text en © 2017 The Authors http://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
Wang, Xiuyan
Rivière, Isabelle
Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title_full Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title_fullStr Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title_full_unstemmed Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title_short Genetic Engineering and Manufacturing of Hematopoietic Stem Cells
title_sort genetic engineering and manufacturing of hematopoietic stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415326/
https://www.ncbi.nlm.nih.gov/pubmed/28480310
http://dx.doi.org/10.1016/j.omtm.2017.03.003
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