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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

To maximize the potential benefits of pulmonary gene therapy, widespread and uniform topical delivery of a viral vector across the surface epithelium is an important goal. Here, we demonstrate an aerosolization technique using a microsprayer positioned intratracheally to deliver a viral vector to newborn pig airways.

Abstract

Gene therapy for airway diseases requires efficient delivery of nucleic acids to the intrapulmonary airways. In small animal models such as mice, gene delivery reagents are commonly delivered as a bolus dose. Routes of delivery may include either nasal sniffing or direct tracheal instillation. However, using a large animal model for preclinical applications is relevant for translation to human trials. Widespread and uniform distribution of transgene expression is critical for developing a successful lung gene therapy treatment. Aerosolizing viral vectors to the lungs of large animals, such as pigs or sheep, is a strategy to maximize gene transfer efficiency and results in greater airway distribution than a liquid bolus dose. Here we demonstrate a technique for direct aerosolization of a viral vector to the airways of newborn pigs. Briefly, a pig is anesthetized, intubated with an endotracheal tube, and a microsprayer is passed through the endotracheal tube. A syringe is used to push the vector through the microsprayer, resulting in a fine mist being released into the distal trachea. The microsprayer produces ~15-16 μm size particles that deposit across the proximal and distal regions of the lung. Using a microsprayer to deliver an adenoviral-based vector, we previously observed ~30-50% of surface epithelial cells transduced in both the large and small airways of newborn pigs.

Introduction

Gene transfer to the lung holds great potential for treating many genetic diseases, such as cystic fibrosis or alpha-1 antitrypsin deficiency. However, developing gene therapy approaches to successfully deliver genes of interest to the airways has been challenging. Animal models play a major role in driving innovation of viral vector design and delivery strategies to the intrapulmonary airways. Indeed, we and others have developed methods to overcome many gene delivery hurdles using large animal models. Many examples of delivery challenges have been previously reviewed1,2,3

Protocol

All animal experiments performed following this protocol must be approved by the respective Institutional Animal Care and Use Committee (IACUC). All procedures described here were approved by the University of Iowa IACUC.

1. Prepare the procedure space and vector delivery materials.

  1. Place a heating pad covered by a disposable underpad to warm the procedure area.
  2. Set up the pulse oximeter to measure the heart rate and peripheral capillary oxygen saturation (SpO2.......

Representative Results

We previously validated this technique for delivering gene transfer vectors to pig lungs and showed widespread and uniform airway distribution following delivery of an adenoviral vector expressing green fluorescent protein (GFP)6. To assess transduction, all six lung lobes were separated into two to four segments. From each segment, tissue was designated for DNA or mRNA isolation and transduction was quantified by real-time PCR to detect the GFP sequence. GFP-posit.......

Discussion

Widespread airway distribution of a viral vector would help ensure the success of a gene therapy approach for treating pulmonary diseases. Here, we demonstrate an aerosolization technique that leads to whole lung expression of large and small pig airways. We describe the steps for sedating a pig, intubating with an ET tube, and aerosolizing a viral vector through the microsprayer aerosolization device. This technique is important as a preclinical approach to testing viral vector efficacy.

Ther.......

Acknowledgements

We thank Christian Brommel for aiding with the airway dissection and Raul Villacreses Rada with the supplemental movie. We thank the University of Iowa Office of Animal Resources and the animal caretakers. We thank the Viral Vector Core for vector production. This work was supported by the National Institutes of Health [NIH P01 HL-51670, NIH P01 HL-091842, NIH R01 HL-133089, NIH R01 HL-105821], the Center for Gene Therapy of Cystic Fibrosis [NIH P30 DK-054759], and the Cystic Fibrosis Foundation [SINN19XX0] and [COONEY18F0].

....

Materials

NameCompanyCatalog NumberComments
AtomizerTeleflexMAD700MADgic Laryngo-Tracheal Mucosal Atomization Device
Compressed Oxygen (O2) gasPraxairAlso need pressure regulator and flowmeter
Disposable underpadGeneral stores
Endotracheal (ET) tube 2.0 mm I.D.Teleflex Medical5-10404Hudson RCI; Sheridan Uncuffed
Fluorescent Dissecting MicroscopeLeicaMDG41
Heating padGeneral stores
IsofluranePharmacy
Isoflurane F/Air Filter CanisterVetamac AnesthesiaSKU VAD020
Isoflurane regulator (vaporizer)Vetamac Anesthesia
Laryngoscope traditional setDarvallVet#80704" blade used for delivery
Leur locking syringe (3 ml)General stores
Lubricating jellyGeneral stores
MicrosprayerPennCenturyAerosolizing catheter; No longer available
Pressurized aerosolizing catheterTrudell Medical CorporationAeroprobe; No longer available
Pulse oximeterPacific Medical SupplyUQNE4600
SpO2 sensor bandHospital stores
StyletHospital stores5 Fr (1.7 mm O.D.)
Thermometer (Digital)General stores
Veterinary anesthesia maskHospital stores
Viral vectorsUniversity of Iowa Viral Vector CoreAdenoviral vector; fee for service

References

  1. Koehler, D. R., Hitt, M. M., Hu, J. Challenges and strategies for cystic fibrosis lung gene therapy. Molecular Therapy. 4 (2), 84-91 (2001).
  2. Oakland, M., Sinn, P. L., McCray, P. B. Advances in cell and gene-based t....

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porcinegene transfermicrosprayerintubationviral vector deliverygene therapy

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