Intramyocardial Transplantation of Autologous CD34 <sup>+</sup> Stem Cells for Intractable Angina

Douglas W. Losordo(Northwestern University), Richard A. Schatz(Northwestern University), Christopher J. White(Northwestern University), James E. Udelson(Northwestern University), Vimal Veereshwarayya(Northwestern University), Michelle Durgin(Northwestern University), Kian Keong Poh(Northwestern University), Robert S. Weinstein(Northwestern University), Marianne Kearney(Northwestern University), M. Siddique Chaudhry(Northwestern University), Aaron Burg(Northwestern University), Liz Eaton(Northwestern University), Lindsay Heyd(Northwestern University), Tina Thorne(Northwestern University), Leon Shturman(Northwestern University), Peter Hoffmeister(Northwestern University), Ken Story(Northwestern University), Victor Zak(Northwestern University), Douglas Dowling(Northwestern University), Jay H. Traverse(Northwestern University), Rachel Olson(Northwestern University), Janice Flanagan(Northwestern University), Donata Sodano(Northwestern University), Toshinori Murayama(Northwestern University), Atsuhiko Kawamoto(Northwestern University), Kengo Kusano(Northwestern University), Jill Wollins(Northwestern University), Frederick G.P. Welt(Northwestern University), Pinak Shah(Northwestern University), Peter Soukas(Northwestern University), Takayuki Asahara(Northwestern University), Timothy D. Henry(Northwestern University)
Circulation
June 12, 2007
Cited by 557Open Access
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Abstract

BACKGROUND: A growing population of patients with coronary artery disease experiences angina that is not amenable to revascularization and is refractory to medical therapy. Preclinical studies have indicated that human CD34+ stem cells induce neovascularization in ischemic myocardium, which enhances perfusion and function. METHODS AND RESULTS: Twenty-four patients (19 men and 5 women aged 48 to 84 years) with Canadian Cardiovascular Society class 3 or 4 angina who were undergoing optimal medical treatment and who were not candidates for mechanical revascularization were enrolled in a double-blind, randomized (3:1), placebo-controlled dose-escalating study. Patients received granulocyte colony-stimulating factor 5 microg x kg(-1) x d(-1) for 5 days with leukapheresis on the fifth day. Selection of CD34+ cells was performed with a Food and Drug Administration-approved device. Electromechanical mapping was performed to identify ischemic but viable regions of myocardium for injection of cells (versus saline). The total dose of cells was distributed in 10 intramyocardial, transendocardial injections. Patients were required to have an implantable cardioverter-defibrillator or to temporarily wear a LifeVest wearable defibrillator. No incidence was observed of myocardial infarction induced by mobilization or intramyocardial injection. The intramyocardial injection of cells or saline did not result in cardiac enzyme elevation, perforation, or pericardial effusion. No incidence of ventricular tachycardia or ventricular fibrillation occurred during the administration of granulocyte colony-stimulating factor or intramyocardial injections. One patient with a history of sudden cardiac death/ventricular tachycardia/ventricular fibrillation had catheter-induced ventricular tachycardia during mapping that required cardioversion. Serious adverse events were evenly distributed. Efficacy parameters including angina frequency, nitroglycerine usage, exercise time, and Canadian Cardiovascular Society class showed trends that favored CD34+ cell-treated patients versus control subjects given placebo. CONCLUSIONS: A randomized trial of intramyocardial injection of autologous CD34+ cells in patients with intractable angina was completed that provides evidence for feasibility, safety, and bioactivity. A larger phase IIb study is currently under way to further evaluate this therapy.


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