James J. Pilla1, Jabaris D. Swain, Michael
G. Katz, Anthony Fargnoli, Marina Sumaroka, Catherine Tomasulo, Mihail
Petrov, Rose Nolen-Walston, JanLee Jensen, Hansell Stedman, Walter J. Koch2,
Joseph Rabinowitz2, Charles R. Bridges
1University of Pennsylvania,
Philadelphia, PA,
United States; 2Thomas
Jefferson University
Genetic
modulation of ventricular function and remodeling may offer a novel therapeutic
strategy for patients with acute ischemic left ventricular (LV) dysfunction. We hypothesize that ARKct
gene therapy will amplify the cardiac response to a beta-adrenergic agonist
resulting in improved function and efficiency as measured by MRI. MRI generated PV loops demonstrated that
ARKct expression improves global LV
systolic performance and efficiency relative to controls. These results in a normal ovine subject,
using a novel, cardiac-specific gene delivery platform (MCARDTM) are
predictive of long term efficacy in a clinically relevant large animal HF
model.