Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis

Mol Ther. 2014 Aug;22(8):1472-1483. doi: 10.1038/mt.2014.87. Epub 2014 May 29.

Abstract

Regulated transgene expression may improve the safety and efficacy of hematopoietic stem cell (HSC) gene therapy. Clinical trials for X-linked chronic granulomatous disease (X-CGD) employing gammaretroviral vectors were limited by insertional oncogenesis or lack of persistent engraftment. Our novel strategy, based on regulated lentiviral vectors (LV), targets gp91(phox) expression to the differentiated myeloid compartment while sparing HSC, to reduce the risk of genotoxicity and potential perturbation of reactive oxygen species levels. Targeting was obtained by a myeloid-specific promoter (MSP) and posttranscriptional, microRNA-mediated regulation. We optimized both components in human bone marrow (BM) HSC and their differentiated progeny in vitro and in a xenotransplantation model, and generated therapeutic gp91(phox) expressing LVs for CGD gene therapy. All vectors restored gp91(phox) expression and function in human X-CGD myeloid cell lines, primary monocytes, and differentiated myeloid cells. While unregulated LVs ectopically expressed gp91(phox) in CD34(+) cells, transcriptionally and posttranscriptionally regulated LVs substantially reduced this off-target expression. X-CGD mice transplanted with transduced HSC restored gp91(phox) expression, and MSP-driven vectors maintained regulation during BM development. Combining transcriptional (SP146.gp91-driven) and posttranscriptional (miR-126-restricted) targeting, we achieved high levels of myeloid-specific transgene expression, entirely sparing the CD34(+) HSC compartment. This dual-targeted LV construct represents a promising candidate for further clinical development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD34 / metabolism
  • Cell Line
  • Cells, Cultured
  • Combined Modality Therapy
  • Disease Models, Animal
  • Genetic Therapy / methods*
  • Genetic Vectors / therapeutic use
  • Granulomatous Disease, Chronic / pathology
  • Granulomatous Disease, Chronic / therapy*
  • Hematopoietic Stem Cell Transplantation / methods*
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / virology*
  • Humans
  • Lentivirus / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • MicroRNAs / genetics*
  • Myeloid Cells / metabolism
  • NADPH Oxidase 2
  • NADPH Oxidases / metabolism*

Substances

  • Antigens, CD34
  • Membrane Glycoproteins
  • MicroRNAs
  • CYBB protein, human
  • NADPH Oxidase 2
  • NADPH Oxidases