Key result
Intracoronary delivery of Ad5.FGF4 improved regional myocardial function in a porcine model of ischemia despite preexisting anti-Ad5 antibodies or prior Ad5 exposure (p<0.001).
Why the study?
Does intracoronary delivery of Ad5.FGF4 improve regional myocardial function in a porcine model of ischemia despite preexisting anti-adenoviral antibodies?
Does intracoronary delivery of Ad5.FGF4 improve regional myocardial function in a porcine model of ischemia despite preexisting anti-adenoviral antibodies?
Intracoronary delivery of Ad5.FGF4 improves regional myocardial function in a porcine model of ischemia even in the presence of preexisting anti-adenoviral antibodies.
Supports preclinical advancement of Ad5.FGF4 for ischemia; leaves open clinical translation in patients with anti-adenoviral antibodies.
The presence of anti-adenoviral serotype 5 (Ad5) antibodies may limit the efficacy of Ad5-mediated gene transfer. We therefore tested the hypothesis that intracoronary delivery of an adenovirus encoding human fibroblast growth factor type 4 (Ad5.FGF4) would improve regional myocardial function in an animal model of ischemia when high antibody levels preexist or after a prior intracoronary dose of Ad5. High anti-Ad5 antibody levels were generated in pigs by subcutaneous immunization with an adenovirus encoding LacZ (Ad5.lacZ). Neutralizing antibody levels increased 648-fold (range, 82- to 2108-fold) above preimmunization levels, and persisted for the duration of the study. Myocardial function during pacing-induced ischemia was improved in the ischemic region (p<0.001) at both 2 and 4 weeks after Ad5.FGF4 administration despite the presence of preexisting antibodies to Ad5. In a second set of experiments, the efficacy of a second intracoronary administration of Ad5 was determined by exposing the animals first to an intracoronary dose of Ad5.lacZ, followed 7 weeks later by the therapeutic dose of Ad5.FGF4. After delivery of Ad5.lacZ, anti-Ad5 antibody levels increased 8-fold (range, 1- to 18-fold), but this prior exposure to Ad5 did not prevent the therapeutic effects after subsequent intracoronary dosing with Ad5.FGF4 (p<0.001). In the porcine Ameroid constrictor model of myocardial ischemia the presence of anti-Ad5 antibodies or prior intracoronary dosing with adenovirus does not prevent the ability of Ad5.FGF4, delivered by intracoronary injection, from normalizing regional myocardial function.
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Roth et al. (2006) studied Myocardial ischemia (animal model). Intracoronary delivery of Ad5.FGF4 was evaluated on Regional myocardial function during pacing-induced ischemia (p=<0.001). Intracoronary delivery of Ad5.FGF4 improved regional myocardial function in a porcine model of ischemia despite preexisting anti-Ad5 antibodies or prior Ad5 exposure (p<0.001).
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