Aerosol delivery of an enhanced helper-dependent adenovirus formulation to rabbit lung using an intratracheal catheter
✍ Scribed by David R. Koehler; Helena Frndova; Kitty Leung; Emily Louca; Donna Palmer; Philip Ng; Colin McKerlie; Peter Cox; Allan L. Coates; Jim Hu
- Book ID
- 102891335
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 607 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1099-498X
- DOI
- 10.1002/jgm.797
No coin nor oath required. For personal study only.
✦ Synopsis
Background Poor transduction of the ciliated airway epithelium and inefficient airway delivery of viral vectors are common difficulties encountered in lung gene therapy trials with large animals and humans.
Methods
We delivered a helper-dependent adenovirus vector, incorporating a human epithelial cell-specific expression cassette, to rabbit lung. An intratracheal device was used to aerosolize a moderate dose of virus (5 × 10 11 particles), mixed with the enhancing agent LPC (L-αlysophosphatidylcholine), directly into the airways. Lung mechanics, body weight and temperature, transgene expression and histopathology were studied at day 5.
Results
Transgene expression was seen in the epithelium of large and small airways, from trachea to terminal bronchioles, with a strong tendency toward the right lung. All cell types of the surface epithelium were transduced. Extensive transduction of the epithelium (66% of cells in trachea) was obtained using virus formulated in isotonic 0.1% LPC, while virus formulated in 0.01% LPC transduced fewer cells (24% in trachea). A transient decrease in dynamic lung compliance was observed immediately following aerosol delivery. Fever and mild-to-moderate patchy pneumonia without edema were also observed.
Conclusion
These data demonstrate a strategy for efficient and effective transduction of airway epithelium in a large animal.