TY - JOUR
T1 - Cell therapy with autologous bone marrow mononuclear stem cells is associated with superior cardiac recovery compared with use of nonmodified mesenchymal stem cells in a canine model of chronic myocardial infarction
AU - Mathieu, Myrielle
AU - Bartunek, J.
AU - Oumeiri, El, B.
AU - Touihri, K.
AU - Hadad, I.
AU - Thoma, Philippe
AU - Metens, T.
AU - Costa, da, A.M.
AU - Mahmoudabady, M.
AU - Egrise, D.
AU - Blocklet, D.
AU - Mazouz, N.
AU - Naeije, R.
AU - Heyndrickx, G.R.
AU - McEntee, K.
PY - 2009
Y1 - 2009
N2 - Objective: Stem cell therapy can facilitate cardiac repair in infarcted myocardium, but the optimal cell type remains uncertain. We conducted a randomized, blind, and placebo-controlled comparison of autologous bone marrow mononuclear cell and mesenchymal stem cell therapy in a large-animal model of chronic myocardial infarction. Methods: Eleven weeks after coronary ligation, 24 dogs received intramyocardial injections of mononuclear cells (227.106 ± 32.106 cells), mesenchymal stem cells (232.106 ± 40.106 cells), or placebo (n = 8 per group). Cardiac performance and remodeling were assessed up to 16 weeks' follow-up. Results: At echocardiographic analysis, the wall motion score index showed a sustained improvement after mononuclear cell transfer (from 1.8 ± 0.1 to 1.5 ± 0.07) and a moderate late improvement after mesenchymal stem cell transfer (from 1.9 ± 0.08 to 1.7 ± 0.1). After mononuclear cell transfer, end-systolic elastance increased (from 2.23 ± 0.25 to 4.42 ± 0.55 mm Hg/mL), infarct size decreased (from 13% ± 0.67% to 10% ± 1.17%), N-terminal B-type natriuretic propeptide level decreased (from 608 ± 146 to 353 ± 118 pmol/L), and relative wall area and arterial density increased. Vascular endothelial growth factor receptor 2 expression was upregulated in the border zone. No change in cardiac contractility or histologic parameters was noted in the mesenchymal stem cell group. Conclusion: In a canine model of chronic myocardial infarction, bone marrow mononuclear cell transfer is superior to mesenchymal stem cell transfer in improvement of cardiac contractility and regional systolic function and reduction in infarct size and plasma N-terminal B-type natriuretic propeptide level. Functional improvement is associated with a favorable angiogenic environment and neovascularization. © 2009 The American Association for Thoracic Surgery.
AB - Objective: Stem cell therapy can facilitate cardiac repair in infarcted myocardium, but the optimal cell type remains uncertain. We conducted a randomized, blind, and placebo-controlled comparison of autologous bone marrow mononuclear cell and mesenchymal stem cell therapy in a large-animal model of chronic myocardial infarction. Methods: Eleven weeks after coronary ligation, 24 dogs received intramyocardial injections of mononuclear cells (227.106 ± 32.106 cells), mesenchymal stem cells (232.106 ± 40.106 cells), or placebo (n = 8 per group). Cardiac performance and remodeling were assessed up to 16 weeks' follow-up. Results: At echocardiographic analysis, the wall motion score index showed a sustained improvement after mononuclear cell transfer (from 1.8 ± 0.1 to 1.5 ± 0.07) and a moderate late improvement after mesenchymal stem cell transfer (from 1.9 ± 0.08 to 1.7 ± 0.1). After mononuclear cell transfer, end-systolic elastance increased (from 2.23 ± 0.25 to 4.42 ± 0.55 mm Hg/mL), infarct size decreased (from 13% ± 0.67% to 10% ± 1.17%), N-terminal B-type natriuretic propeptide level decreased (from 608 ± 146 to 353 ± 118 pmol/L), and relative wall area and arterial density increased. Vascular endothelial growth factor receptor 2 expression was upregulated in the border zone. No change in cardiac contractility or histologic parameters was noted in the mesenchymal stem cell group. Conclusion: In a canine model of chronic myocardial infarction, bone marrow mononuclear cell transfer is superior to mesenchymal stem cell transfer in improvement of cardiac contractility and regional systolic function and reduction in infarct size and plasma N-terminal B-type natriuretic propeptide level. Functional improvement is associated with a favorable angiogenic environment and neovascularization. © 2009 The American Association for Thoracic Surgery.
U2 - 10.1016/j.jtcvs.2008.12.031
DO - 10.1016/j.jtcvs.2008.12.031
M3 - Article
C2 - 19698851
SN - 0022-5223
VL - 138
SP - 646
EP - 653
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
IS - 3
ER -