Autologous skeletal myoblasts transplanted to ischemia-damaged myocardium in humans - Histological analysis of cell survival and differentiation

被引:351
作者
Pagani, FD
DerSimonian, H
Zawadzka, A
Wetzel, K
Edge, ASB
Jacoby, DB
Dinsmore, JH
Wright, S
Aretz, TH
Eisen, HJ
Aaronson, KD
机构
[1] Univ Michigan, Sect Cardiac Surg, Heart Transplant Program, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Div Cardiol, Ann Arbor, MI 48109 USA
[3] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[4] Temple Univ, Philadelphia, PA 19122 USA
[5] Diacrin Inc, Charlestown, MA USA
关键词
D O I
10.1016/S0735-1097(03)00081-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES We report histological analysis of hearts from patients with end-stage heart disease who were transplanted with autologous skeletal myoblasts concurrent with left ventricular assist device (LVAD) implantation. BACKGROUND Autologous skeletal myoblast transplantation is under investigation as a means to repair infarcted myocardium. To date, there is only indirect evidence to suggest survival of skeletal muscle in humans. METHODS Five patients (all male; median age 60 years) with ischemic cardiomyopathy, refractory heart failure, and listed for heart transplantation underwent muscle biopsy from the quadriceps muscle. The muscle specimen was shipped to a cell isolation facility where myoblasts were isolated and grown. Patients received a transplant of 300 million cells concomitant with LVAD implantation. Four patients underwent LVAD explant after 68, 91, 141, and 191 days of LVAD support (three transplant, one LVAD death), respectively. One patient remains alive on LVAD support awaiting heart transplantation. RESULTS Skeletal muscle cell survival and differentiation into mature myofibers were directly demonstrated in scarred myocardium from three of the four explanted hearts using an antibody against skeletal muscle-specific myosin heavy chain. An increase in small vessel formation was observed in one of three patients at the site of surviving myotubes, but not in adjacent tissue devoid of engrafted cells. CONCLUSIONS These findings represent demonstration of autologous myoblast cell survival in human heart. The implanted skeletal myoblasts formed viable grafts in heavily scarred human myocardial tissue. These results establish the feasibility of myoblast transplants for myocardial repair in humans. (C) 2003 by the American College of Cardiology Foundation.
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页码:879 / 888
页数:10
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