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Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy
We have developed a producer cell line that generates lentiviral vector particles of high titer. The vector encodes the Wiskott-Aldrich syndrome (WAS) protein. An insulator element has been added to the long terminal repeats of the integrated vector to limit proto-oncogene activation. The vector pro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449020/ https://www.ncbi.nlm.nih.gov/pubmed/26052531 http://dx.doi.org/10.1038/mtm.2014.63 |
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author | Wielgosz, Matthew M Kim, Yoon-Sang Carney, Gael G Zhan, Jun Reddivari, Muralidhar Coop, Terry Heath, Richard J Brown, Scott A Nienhuis, Arthur W |
author_facet | Wielgosz, Matthew M Kim, Yoon-Sang Carney, Gael G Zhan, Jun Reddivari, Muralidhar Coop, Terry Heath, Richard J Brown, Scott A Nienhuis, Arthur W |
author_sort | Wielgosz, Matthew M |
collection | PubMed |
description | We have developed a producer cell line that generates lentiviral vector particles of high titer. The vector encodes the Wiskott-Aldrich syndrome (WAS) protein. An insulator element has been added to the long terminal repeats of the integrated vector to limit proto-oncogene activation. The vector provides high-level, stable expression of WAS protein in transduced murine and human hematopoietic cells. We have also developed a monoclonal antibody specific for intracellular WAS protein. This antibody has been used to monitor expression in blood and bone marrow cells after transfer into lineage negative bone marrow cells from WAS mice and in a WAS negative human B-cell line. Persistent expression of the transgene has been observed in transduced murine cells 12–20 weeks following transplantation. The producer cell line and the specific monoclonal antibody will facilitate the development of a clinical protocol for gene transfer into WAS protein deficient stem cells. |
format | Online Article Text |
id | pubmed-4449020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44490202015-06-05 Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy Wielgosz, Matthew M Kim, Yoon-Sang Carney, Gael G Zhan, Jun Reddivari, Muralidhar Coop, Terry Heath, Richard J Brown, Scott A Nienhuis, Arthur W Mol Ther Methods Clin Dev Article We have developed a producer cell line that generates lentiviral vector particles of high titer. The vector encodes the Wiskott-Aldrich syndrome (WAS) protein. An insulator element has been added to the long terminal repeats of the integrated vector to limit proto-oncogene activation. The vector provides high-level, stable expression of WAS protein in transduced murine and human hematopoietic cells. We have also developed a monoclonal antibody specific for intracellular WAS protein. This antibody has been used to monitor expression in blood and bone marrow cells after transfer into lineage negative bone marrow cells from WAS mice and in a WAS negative human B-cell line. Persistent expression of the transgene has been observed in transduced murine cells 12–20 weeks following transplantation. The producer cell line and the specific monoclonal antibody will facilitate the development of a clinical protocol for gene transfer into WAS protein deficient stem cells. Nature Publishing Group 2015-01-21 /pmc/articles/PMC4449020/ /pubmed/26052531 http://dx.doi.org/10.1038/mtm.2014.63 Text en Copyright © 2015 American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Wielgosz, Matthew M Kim, Yoon-Sang Carney, Gael G Zhan, Jun Reddivari, Muralidhar Coop, Terry Heath, Richard J Brown, Scott A Nienhuis, Arthur W Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title | Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title_full | Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title_fullStr | Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title_full_unstemmed | Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title_short | Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy |
title_sort | generation of a lentiviral vector producer cell clone for human wiskott-aldrich syndrome gene therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449020/ https://www.ncbi.nlm.nih.gov/pubmed/26052531 http://dx.doi.org/10.1038/mtm.2014.63 |
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