Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wielgosz, Matthew M, Kim, Yoon-Sang, Carney, Gael G, Zhan, Jun, Reddivari, Muralidhar, Coop, Terry, Heath, Richard J, Brown, Scott A, Nienhuis, Arthur W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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
_version_ 1782373804308168704
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
work_keys_str_mv AT wielgoszmatthewm generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT kimyoonsang generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT carneygaelg generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT zhanjun generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT reddivarimuralidhar generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT coopterry generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT heathrichardj generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT brownscotta generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy
AT nienhuisarthurw generationofalentiviralvectorproducercellcloneforhumanwiskottaldrichsyndromegenetherapy