Biological therapies for conduction system disorders

International Meeting on Clinical Case Reports

April 18-20, 2016 Dubai, UAE

Cingolani Eugenio

Cedars Sinai Heart Institute, USA

Posters & Accepted Abstracts: J Clin Case Rep

Abstract :

Gene based BioP were first described more than a decade ago; somatic gene transfer of various constructs (a dominant negative mutant of the inward rectifier channel [Kir2.1AAA], wild type HCN channels and a transcription factor [Tbx18]) have all been shown to create BioP activity. However, until recently, in vivo preclinical applications have been mostly limited to highly invasive open chest models. We have developed a clinically realistic minimally invasive delivery technique and used it to create BioP in a porcine model of complete heart block. Here, we propose to use this approach to compare two â�?�?finalistâ�? therapeutic candidates with fundamentally different mechanisms of action. The first one is a wild type ion channel (HCN2) that artificially induces automaticity in ventricular cardiomyocytes by functional re-engineering. The goal is not to create a faithful replica of a pacemaker cell, but rather to manipulate a single component of the membrane channel repertoire so as to induce spontaneous firing in an excitable but normally quiescent cell. The active principle of the second therapeutic candidate, Tbx18, reprograms ventricular cardiomyocytes into sinoatrial node (SAN) like pacemaker cells (induced SAN [iSAN] cells). No one determinant of excitability is selectively overexpressed: The entire gene expression program is altered with resultant changes in fundamental cell physiology and morphology. The proposal utilizes the above mentioned percutaneous delivery method to reduce to refine and validate in a large animal model of bradycardia, the approaches required for translation to the clinic. We will characterize and compare the pacing efficacy and safety of HCN2 and Tbx18 derived BioP, testing the hypothesis that iSAN cells will provide superior chronotropic support as compared to HCN2. We will go on to perform long term efficacy, toxicology and bio distribution studies with the more promising therapeutic candidate and then prepare and obtain approval of an Investigational New Drug (IND) application for a first-in-human BioP trial. While the ultimate goal may be to render obsolete the electronic pacemaker, it is important to be realistic in thinking about potential first-inhuman applications. Therefore, we have chosen to develop a bridge to device product that will temporarily provide hardware free chronotropic support in infected patients who are pacemaker dependent. To make BioP temporary, we deliver the genes in adenoviral vectors, relying on immunological clearance to limit bioactivity. Nevertheless, we will test catheter ablation of the BioP as a backup rescue strategy in case of persistent undesired BioP activity. This research proposal is designed to lay the groundwork for clinical testing of an optimized BioP in a needy patient population. Device related infections continue to rise in the USA. A temporary BioP could represent a future alternative hardware free â�?�?bridgeâ�? for those afflicted by device related complications.

Biography :

Email: Eugenio.Cingolani@csmc.edu