| Literature DB >> 24831844 |
Samuel Chauveau1, Peter R Brink1, Ira S Cohen2.
Abstract
Electronic pacemakers are the standard therapy for bradycardia-related symptoms but have shortcomings. Over the past 15 years, experimental evidence has demonstrated that gene and cell-based therapies can create a biological pacemaker. Recently, physiologically acceptable rates have been reported with an adenovirus-based approach. However, adenovirus-based protein expression does not last more than 4 weeks, which limits its clinical applicability. Cell-based platforms are potential candidates for longer expression. Currently there are two cell-based approaches being tested: (i) mesenchymal stem cells used as a suitcase for delivering pacemaker genes and (ii) pluripotent stem cells differentiated down a cardiac lineage with endogenous pacemaker activity. This review examines the current achievements in engineering a biological pacemaker, defines the patient population for whom this device would be useful and identifies the challenges still ahead before cell therapy can replace current electronic devices.Entities:
Keywords: arrhythmia therapy; cell therapy; gene therapy; pacemaker
Mesh:
Year: 2014 PMID: 24831844 PMCID: PMC4051829 DOI: 10.1016/j.jcyt.2014.02.014
Source DB: PubMed Journal: Cytotherapy ISSN: 1465-3249 Impact factor: 5.414