Catheter-based intramyocardial delivery (NavX) of adenovirus achieves safe and accurate gene transfer in pigs

PLoS One. 2013;8(1):e53007. doi: 10.1371/journal.pone.0053007. Epub 2013 Jan 3.

Abstract

Background: Hepatocyte growth factor (HGF) is one of the major angiogenic factors being studied for the treatment of ischemic heart diseases. Our previous study demonstrated adenovirus-HGF was effective in myocardial ischemia models. The first clinical safety study showed a positive effect in patients with severe and diffused triple coronary disease.

Methods: 12 Pigs were randomized (1:1) to receive HGF, which was administered as five injections into the infarcted myocardium, or saline (control group). The injections were guided by EnSite NavX left ventricular electroanatomical mapping.

Results: The catheter-based injections caused no pericardial effusion, malignant arrhythmia or death. During mapping and injection, alanine aminotransferase, aspartate aminotransferase, blood urea nitrogen, serum creatinine and creatine kinase-MB levels have no significant increase as compared to those before and after the injection in HGF group(P>0.05). HGF group has high HGF expression with Western blot, less myocardial infarct sizes by electroanatomical mapping (HGF group versus after saline group, 5.28 ± 0.55 cm(2) versus 9.06 ± 1.06 cm(2), P<0.01), better cardiac function with Gated-Single Photon Emission Computed Tomography compared with those in saline group. Histological, strongly increased lectin-positive microvessels and microvessel density were found in the myocardial ischemic regions in HGF group.

Conclusion: Intramyocardial injection guided by NavX system provides a method of feasible and safe percutaneous gene transfer to myocardial infarct regions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Catheterization
  • Gene Transfer Techniques*
  • Genetic Therapy / methods
  • Genetic Vectors
  • HEK293 Cells
  • Heart Ventricles / pathology
  • Hepatocyte Growth Factor / genetics*
  • Humans
  • Male
  • Myocardial Ischemia / pathology
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Random Allocation
  • Reproducibility of Results
  • Swine
  • Swine, Miniature
  • Tomography, Emission-Computed, Single-Photon / methods

Substances

  • Hepatocyte Growth Factor

Grants and funding

This work was financially supported by grants from National Nature Science Foundation of China (30971254), Supporting Program of Science and Technology of Jiangsu (Social Development, BE2009686), the Innovative Project of Clamber Scholar of Jiangsu (BK2010021), Chinese National Basic Research and Development Grants ‘973’ (2008CB517303), the National Mega-Project of Science Research of China (No.2009ZX09301-002) and Chinese High-Tech Grant‘863’(2007AA021007), and a Project Funded by the Priority Acadamic Program Development of Jiangsu Higher Education Institutions. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.