Key result
AAV9.IGF-1Ea improves LVEF and reduces adverse cardiac remodeling post-MI in mice.
Why the study?
The therapeutic potential of IGF-1Ea for improving cardiac repair and preventing adverse remodelling after myocardial infarction was investigated using targeted gene delivery.
Does intravenous AAV9-mediated IGF-1Ea gene therapy improve left ventricular remodelling in mice after myocardial infarction?
Does intravenous AAV9-mediated IGF-1Ea gene therapy improve left ventricular remodelling in mice after myocardial infarction?
Intravenous AAV9-mediated IGF-1Ea gene therapy improves post-infarct cardiac remodelling and left ventricular function in a mouse model.
The insulin-like growth factor Ea propeptide (IGF-1Ea) is a powerful enhancer of cardiac muscle growth and regeneration, also blocking age-related atrophy and beneficial in multiple skeletal muscle diseases. The therapeutic potential of IGF-1Ea compared with mature IGF-1 derives from its local action in the area of synthesis. We have developed an adeno-associated virus (AAV) vector for IGF-1Ea delivery to the heart to treat mice after myocardial infarction and examine the reparative effects of local IGF-1Ea production on left ventricular remodelling. A cardiotropic AAV9 vector carrying a cardiomyocyte-specific IGF-1Ea-luciferase bi-cistronic gene expression cassette (AAV9.IGF-1Ea) was administered intravenously to infarcted mice, 5 h after ischemia followed by reperfusion (I/R), as a model of myocardial infarction. Virally encoded IGF-1Ea in the heart improved global left ventricular function and remodelling, as measured by wall motion and thickness, 28 days after delivery, with higher viral titers yielding better improvement. The present study demonstrates that single intravenous AAV9-mediated IGF-1Ea Gene Therapy represents a tissue-targeted therapeutic approach to prevent the adverse remodelling after myocardial infarct.
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Gallego-Colón et al. (2016) studied Myocardial Infarction (n=140). AAV9.IGF-1Ea vs. No viral treatment (I/R) and AAV9.GFP was evaluated on Left ventricular ejection fraction and cardiac remodelling at 28 days post-infarction (p=<0.05). A single intravenous injection of AAV9.IGF-1Ea significantly improved left ventricular ejection fraction and reduced adverse cardiac remodelling 28 days after myocardial infarction in mice.
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