High ionic strength vector formulations enhance gene transfer to airway epithelia.
Ashley L CooneyLaura Marquez LozaKenan NajdawiChristian M BrommelPaul B McCrayPatrick L SinnPublished in: Nucleic acids research (2024)
A fundamental challenge for cystic fibrosis (CF) gene therapy is ensuring sufficient transduction of airway epithelia to achieve therapeutic correction. Hypertonic saline (HTS) is frequently administered to people with CF to enhance mucus clearance. HTS transiently disrupts epithelial cell tight junctions, but its ability to improve gene transfer has not been investigated. Here, we asked if increasing the concentration of NaCl enhances the transduction efficiency of three gene therapy vectors: adenovirus, AAV, and lentiviral vectors. Vectors formulated with 3-7% NaCl exhibited markedly increased transduction for all three platforms, leading to anion channel correction in primary cultures of human CF epithelial cells and enhanced gene transfer in mouse and pig airways in vivo. The mechanism of transduction enhancement involved tonicity but not osmolarity or pH. Formulating vectors with a high ionic strength solution is a simple strategy to greatly enhance efficacy and immediately improve preclinical or clinical applications.
Keyphrases
- gene therapy
- cystic fibrosis
- pseudomonas aeruginosa
- genome wide
- lung function
- ionic liquid
- genome wide identification
- endothelial cells
- blood brain barrier
- dna methylation
- gene expression
- stem cells
- solid state
- single molecule
- mesenchymal stem cells
- genome wide analysis
- chronic obstructive pulmonary disease
- transcription factor
- mass spectrometry
- pluripotent stem cells