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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.
Afiliação
  • Wielgosz MM; Division of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Kim YS; Division of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Carney GG; Division of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Zhan J; Division of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Reddivari M; Department of Infectious Diseases, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Coop T; Department of Infectious Diseases, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Heath RJ; Department of Infectious Diseases, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Brown SA; Immunology Department, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
  • Nienhuis AW; Division of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee, USA.
Mol Ther Methods Clin Dev ; 2: 14063, 2015.
Article em En | MEDLINE | ID: mdl-26052531
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Mol Ther Methods Clin Dev Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Mol Ther Methods Clin Dev Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos