Intramyocardial Injection of Autologous Cardiospheres or Cardiosphere-Derived Cells Preserves Function and Minimizes Adverse Ventricular Remodeling in Pigs With Heart Failure Post-Myocardial Infarction

被引:197
作者
Lee, Shuo-Tsan [1 ]
White, Anthony J. [1 ]
Matsushita, Satoshi [1 ]
Malliaras, Konstantinos [1 ]
Steenbergen, Charles [2 ]
Zhang, Yiqiang [1 ]
Li, Tao-Sheng [1 ]
Terrovitis, John [1 ]
Yee, Kristine [1 ]
Simsir, Sinan [1 ]
Makkar, Raj [1 ]
Marban, Eduardo [1 ]
机构
[1] Cedars Sinai Heart Inst, Los Angeles, CA USA
[2] Johns Hopkins Univ, Dept Pathol, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
animal model; cardiosphere-derived cell; heart failure; myocardial infarction; stem cell; ACUTE MYOCARDIAL-INFARCTION; CARDIAC STEM-CELLS; TRANSPLANTATION; OPTIMIZATION; REGENERATION; METAANALYSIS; EXPANSION; SURVIVAL; REPAIR;
D O I
10.1016/j.jacc.2010.07.049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study was to test the safety and efficacy of direct injection of cardiosphere-derived cells (CDCs) and their 3-dimensional precursors, cardiospheres, for cellular cardiomyoplasty in a mini-pig model of heart failure after myocardial infarction. Background Intracoronary administration of CDCs has been demonstrated to reduce infarct size and improve hemodynamic indexes in the mini-pig model, but intramyocardial injection of CDCs or cardiospheres has not been assessed in large animals. Methods Autologous cardiospheres or CDCs grown from endomyocardial biopsies were injected through thoracotomy 4 weeks after anteroseptal myocardial infarction. Engraftment optimization with luciferase-labeled CDCs guided the choice of cell dose (0.5 million cells/site) and target tissue (20 peri-infarct sites). Pigs were randomly allocated to placebo (n = 11), cardiospheres (n = 8), or CDCs (n = 10). Functional data were acquired before injection and again 8 weeks later, after which organs were harvested for histopathology. Results Beyond the immediate perioperative period, all animals survived to protocol completion. Ejection fraction was equivalent at baseline, but at 8 weeks was higher than placebo in both of the cell-treated groups (placebo vs. CDC, p = 0.01; placebo vs. cardiospheres, p = 0.01). Echocardiographic and hemodynamic indexes of efficacy improved disproportionately with cardiospheres; likewise, adverse remodeling was more attenuated with cardiospheres than with CDCs. Provocative electrophysiologic testing showed no differences among groups, and no tumors were found. Conclusions Dosage-optimized direct injection of cardiospheres or CDCs is safe and effective in preserving ventricular function in porcine ischemic cardiomyopathy. Although CDCs and cardiospheres have equivalent effects on left ventricular ejection fraction, cardiospheres are superior in improving hemodynamics and regional function, and in attenuating ventricular remodeling. (J Am Coll Cardiol 2011; 57: 455-65) (C) 2011 by the American College of Cardiology Foundation
引用
收藏
页码:455 / 465
页数:11
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