Generation of novel AAV variants by directed evolution for improved CFTR delivery to human ciliated airway epithelium

Mol Ther. 2009 Dec;17(12):2067-77. doi: 10.1038/mt.2009.155. Epub 2009 Jul 14.

Abstract

Recombinant adeno-associated virus (AAV) vectors expressing the cystic fibrosis transmembrane conductance regulator (CFTR) gene have been used to deliver CFTR to the airway epithelium of cystic fibrosis (CF) patients. However, no significant CFTR function has been demonstrated likely due to low transduction efficiencies of the AAV vectors. To improve AAV transduction efficiency for human airway epithelium (HAE), we generated a chimeric AAV library and performed directed evolution of AAV on an in vitro model of human ciliated airway epithelium. Two independent and novel AAV variants were identified that contained capsid components from AAV-1, AAV-6, and/or AAV-9. The transduction efficiencies of the two novel AAV variants for human ciliated airway epithelium were three times higher than that for AAV-6. The novel variants were then used to deliver CFTR to ciliated airway epithelium from CF patients. Here we show that our novel AAV variants, but not the parental, AAV provide sufficient CFTR delivery to correct the chloride ion transport defect to ~25% levels measured in non-CF cells. These results suggest that directed evolution of AAV on relevant in vitro models will enable further improvements in CFTR gene transfer efficiency and the development of an efficacious and safe gene transfer vector for CF lung disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cells, Cultured
  • Chlorides / metabolism
  • Cilia / metabolism
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / therapy*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism
  • Dependovirus / genetics*
  • Epithelium / metabolism*
  • Genetic Therapy*
  • Genetic Vectors / therapeutic use*
  • HeLa Cells
  • Humans
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Respiratory System / cytology
  • Respiratory System / metabolism*
  • Transduction, Genetic
  • Transfection

Substances

  • CFTR protein, human
  • Chlorides
  • Recombinant Proteins
  • Cystic Fibrosis Transmembrane Conductance Regulator