Single-dose lentiviral gene transfer for lifetime airway gene expression

J Gene Med. 2009 Oct;11(10):861-7. doi: 10.1002/jgm.1368.

Abstract

Background: Cystic fibrosis (CF) is caused by a defect in cystic fibrosis transmembrane conductance regulator (CFTR) activity, often resulting in an incurable airway disease. Gene therapy into the conducting airway epithelium is a potential cure for CF; however, most gene vectors do not result in long-lived expression, and require re-dosing. Perversely, intrinsic host immune responses can then block renewed gene transfer.

Methods: To investigate whether persistent gene expression could be achieved after a single dosing event, thus avoiding the issue of blocking host responses, we used a gene transfer protocol that combined an airway pretreatment using lysophosphatidylcholine with a human immunodeficiency virus type-1 (vesicular stomatitis virus G pseudotype) derived lentiviral vector to test whether an integrating vector could produce gene expression able to last for a substantial part of the lifetime of the laboratory mouse.

Results: We found that a single dose of LV-LacZ produced immediate as well as lifetime mouse airway expression, confirming our hypothesis that use of an integrating vector extends transgene expression. Importantly, LV-CFTR dosing achieved at least 12 months of CFTR expression, representing partial functional correction of the CFTR defect in CF-null mice.

Conclusions: These findings validate the potential of this methodology for developing a gene transfer treatment for CF airway disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / metabolism
  • Cystic Fibrosis / therapy*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Gene Expression
  • Gene Transfer Techniques*
  • Genetic Therapy / methods
  • Genetic Vectors / administration & dosage*
  • Genetic Vectors / genetics
  • Genetic Vectors / metabolism*
  • HIV-1 / genetics
  • Humans
  • Lentivirus / genetics*
  • Lysophosphatidylcholines / administration & dosage
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CFTR
  • Respiratory Mucosa / drug effects
  • Respiratory Mucosa / metabolism*
  • Time Factors

Substances

  • Lysophosphatidylcholines
  • Cystic Fibrosis Transmembrane Conductance Regulator