Gene therapy for the treatment of heart failure: promise postponed.

Gene therapy has emerged as a powerful tool in targeting the molecular mechanisms implicated in heart failure. Refinements in vector technology, including the development of recombinant adeno-associated vectors, have allowed for safe, long-term, and efficient gene transfer to the myocardium. These advancements, coupled with evolving delivery techniques, have placed gene therapy as a viable therapeutic option for patients with heart failure. However, after much promise in early-phase clinical trials, the more recent larger clinical trials have shown disappointing results, thus forcing the field to re-evaluate current vectors, delivery systems, targets, and endpoints. We provide here an updated review of current cardiac gene therapy programmes that have been or are being translated into clinical trials.

[1]  P. Boekstegers,et al.  Cardiac AAV9-S100A1 Gene Therapy Rescues Post-Ischemic Heart Failure in a Preclinical Large Animal Model , 2011, Science Translational Medicine.

[2]  W. Koch,et al.  Targeting GRK2 by gene therapy for heart failure: benefits above β-blockade , 2012, Gene Therapy.

[3]  Andrew N. Carr,et al.  Enhancement of Cardiac Function and Suppression of Heart Failure Progression By Inhibition of Protein Phosphatase 1 , 2005, Circulation research.

[4]  H. Ly,et al.  Reversal of cardiac dysfunction after long-term expression of SERCA2a by gene transfer in a pre-clinical model of heart failure. , 2008, Journal of the American College of Cardiology.

[5]  M. Regnier,et al.  2-Deoxy adenosine triphosphate improves contraction in human end-stage heart failure. , 2015, Journal of molecular and cellular cardiology.

[6]  L. Zentilin,et al.  Intracoronary Cytoprotective Gene Therapy: A Study of VEGF-B167 in a Pre-Clinical Animal Model of Dilated Cardiomyopathy. , 2015, Journal of the American College of Cardiology.

[7]  D. Sigg,et al.  Cardiac I-1c overexpression with reengineered AAV improves cardiac function in swine ischemic heart failure. , 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

[8]  P. Boekstegers,et al.  Myocardial gene transfer by selective pressure-regulated retroinfusion of coronary veins , 2000, Gene Therapy.

[9]  M. Chillón,et al.  Gutless adenovirus: last-generation adenovirus for gene therapy , 2005, Gene Therapy.

[10]  R. Hajjar,et al.  SERCA2a gene transfer enhances eNOS expression and activity in endothelial cells. , 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

[11]  L. A. Bonet,et al.  ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012 , 2012, Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir.

[12]  E. Kizana,et al.  SUMO1-dependent modulation of SERCA2a in heart failure , 2011, Nature.

[13]  M. Penn,et al.  Plasmid-based transient human stromal cell-derived factor-1 gene transfer improves cardiac function in chronic heart failure , 2011, Gene Therapy.

[14]  G. Fonarow,et al.  Epidemiology and risk profile of heart failure , 2011, Nature Reviews Cardiology.

[15]  W Grossman,et al.  Abnormal intracellular calcium handling in myocardium from patients with end-stage heart failure. , 1987, Circulation research.

[16]  J. Rabinowitz,et al.  Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

[17]  K. Zsebo,et al.  Long-Term Effects of AAV1/SERCA2a Gene Transfer in Patients With Severe Heart Failure: Analysis of Recurrent Cardiovascular Events and Mortality , 2014, Circulation research.

[18]  K. Ishikawa,et al.  Cardiac gene therapy in large animals: bridge from bench to bedside , 2012, Gene Therapy.

[19]  Woo Jin Park,et al.  Restoration of mechanical and energetic function in failing aortic-banded rat hearts by gene transfer of calcium cycling proteins. , 2007, Journal of molecular and cellular cardiology.

[20]  P. Ellinor,et al.  Prevention of Ventricular Arrhythmias With Sarcoplasmic Reticulum Ca2+ ATPase Pump Overexpression in a Porcine Model of Ischemia Reperfusion , 2008, Circulation.

[21]  P. Boekstegers,et al.  Heme Oxygenase-1 Gene Therapy Provides Cardioprotection Via Control of Post-Ischemic Inflammation: An Experimental Study in a Pre-Clinical Pig Model. , 2015, Journal of the American College of Cardiology.

[22]  R. Herzog,et al.  Progress and prospects: immune responses to viral vectors , 2010, Gene Therapy.

[23]  Michael Bader,et al.  SDF-1α as a therapeutic stem cell homing factor in myocardial infarction. , 2011, Pharmacology & therapeutics.

[24]  Houping Ni,et al.  Suppression of RNA recognition by Toll-like receptors: the impact of nucleoside modification and the evolutionary origin of RNA. , 2005, Immunity.

[25]  Ronald A. Li,et al.  Modified mRNA directs the fate of heart progenitor cells and induces vascular regeneration after myocardial infarction , 2013, Nature Biotechnology.

[26]  Akshay S. Desai,et al.  Calcium upregulation by percutaneous administration of gene therapy in patients with cardiac disease (CUPID 2): a randomised, multinational, double-blind, placebo-controlled, phase 2b trial , 2016, The Lancet.

[27]  B. Byrne,et al.  Tissue specific promoters improve specificity of AAV9 mediated transgene expression following intra-vascular gene delivery in neonatal mice , 2008, Genetic vaccines and therapy.

[28]  Amit N. Patel,et al.  Changes in ventricular remodelling and clinical status during the year following a single administration of stromal cell-derived factor-1 non-viral gene therapy in chronic ischaemic heart failure patients: the STOP-HF randomized Phase II trial , 2015, European heart journal.

[29]  Daniel G. Anderson,et al.  Myocardial Delivery of Lipidoid Nanoparticle Carrying modRNA Induces Rapid and Transient Expression. , 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

[30]  H. Sweeney,et al.  Enhancing the utility of adeno-associated virus gene transfer through inducible tissue-specific expression. , 2013, Human gene therapy methods.

[31]  R. Weiss,et al.  Transgenic overexpression of ribonucleotide reductase improves cardiac performance , 2013, Proceedings of the National Academy of Sciences.

[32]  T. Anzai,et al.  Adenylylcyclase increases responsiveness to catecholamine stimulation in transgenic mice. , 1999, Circulation.

[33]  N. Dalton,et al.  Intracoronary Adenovirus Encoding Adenylyl Cyclase VI Increases Left Ventricular Function in Heart Failure , 2004, Circulation.

[34]  A. Remppis,et al.  Stable Myocardial-Specific AAV6-S100A1 Gene Therapy Results in Chronic Functional Heart Failure Rescue , 2007, Circulation.

[35]  Barry Greenberg,et al.  Calcium Upregulation by Percutaneous Administration of Gene Therapy in Cardiac Disease (CUPID): A Phase 2 Trial of Intracoronary Gene Therapy of Sarcoplasmic Reticulum Ca2+-ATPase in Patients With Advanced Heart Failure , 2011, Circulation.