Comparison of insulators and promoters for expression of the Wiskott-Aldrich syndrome protein using lentiviral vectors.

Abstract

Gene therapy for the treatment of Wiskott-Aldrich syndrome (WAS) presents an alternative to the current use of allogeneic bone marrow transplantation. We describe the development of a self-inactivating lentiviral vector containing chromatin insulators for treatment of WAS and compare a gammaretroviral (MND), human cellular (EF1α), and the human WASp gene promoter for expression patterns in vivo during murine hematopoiesis using the green fluorescent protein (GFP) marker. Compared with the EF1α and the WASp promoters, expression from the MND promoter in mouse transplant recipients was much higher in all lineages examined. Importantly, there was sustained expression in the platelets of secondary recipient animals, necessary to correct the thrombocytopenia defect in WAS patients. Analysis of WAS protein expression in transduced human EBV-immortalized B-cells and transduced patient peripheral blood mononuclear cells also demonstrated stronger expression per copy from the MND promoter compared with the other promoters. In addition, when analyzed in an LM02 activation assay, the addition of an insulator to MND-promoter-containing constructs reduced transactivation of the LM02 gene. We propose a clinical trial design in which cytokine-mobilized, autologous, transduced CD34(+) cells are administered after myelosuppression.

• Authors: Rachel M Koldej, Gael Carney, Matthew M Wielgosz, Sheng Zhou, Jun Zhan, Brian P Sorrentino, Arthur W Nienhuis
• Journal: Human gene therapy. Clinical development (Hum Gene Ther Clin Dev) Vol. 24 Issue 2 Pg. 77-85 (Jun 2013) ISSN: 2324-8645 [Electronic] United States
• PMID: 23786330 (Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• CCAAT-Enhancer-Binding Protein-alpha
• Chromatin
• Recombinant Fusion Proteins
• Wiskott-Aldrich Syndrome Protein
• Green Fluorescent Proteins

Topics

• Animals
• B-Lymphocytes (cytology, metabolism)
• Blood Platelets (cytology)
• CCAAT-Enhancer-Binding Protein-alpha (genetics, metabolism)
• Cells, Cultured
• Chromatin (metabolism)
• Gammaretrovirus (genetics)
• Genetic Therapy
• Genetic Vectors (genetics, metabolism)
• Green Fluorescent Proteins (genetics, metabolism)
• Humans
• Lentivirus (genetics)
• Leukocytes, Mononuclear (cytology, metabolism)
• Mice
• Platelet Count
• Promoter Regions, Genetic
• Recombinant Fusion Proteins (biosynthesis, genetics)
• T-Lymphocytes (cytology, metabolism)
• Transduction, Genetic
• Wiskott-Aldrich Syndrome (therapy)
• Wiskott-Aldrich Syndrome Protein (genetics, metabolism)