2005
DOI: 10.1016/j.ijcard.2004.12.007
|View full text |Cite
|
Sign up to set email alerts
|

Autologous intracoronary mononuclear bone marrow cell transplantation in chronic ischemic cardiomyopathy in humans

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

2
34
0

Year Published

2007
2007
2017
2017

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 44 publications
(36 citation statements)
references
References 29 publications
2
34
0
Order By: Relevance
“…This result is consistent with the finding of a previous study in which no therapeutic effect was obtained by cell implantation for chronic ischemic disease. 29 Agreeing well with our in vitro data, the results of our in vivo studies also indicated that the microenvironment of acute ischemic tissues was more conducive to the survival of implanted BMCs and the improvement of blood flow than that of chronic ischemic tissue, suggesting that it would be more beneficial for cell-based therapeutic angiogenesis. Because the microenvironment of acute ischemic tissue is complicated by many increased cytokines and by oxidative stress, [15][16][17] further studies should be done on the effects of cytokine inhibition with neutralizing antibodies on the survival of implanted cells in the acute ischemic tissue, in order to identify the important key cytokines that promote the survival and angiogenic potency of BMCs.…”
Section: Discussionsupporting
confidence: 78%
“…This result is consistent with the finding of a previous study in which no therapeutic effect was obtained by cell implantation for chronic ischemic disease. 29 Agreeing well with our in vitro data, the results of our in vivo studies also indicated that the microenvironment of acute ischemic tissues was more conducive to the survival of implanted BMCs and the improvement of blood flow than that of chronic ischemic tissue, suggesting that it would be more beneficial for cell-based therapeutic angiogenesis. Because the microenvironment of acute ischemic tissue is complicated by many increased cytokines and by oxidative stress, [15][16][17] further studies should be done on the effects of cytokine inhibition with neutralizing antibodies on the survival of implanted cells in the acute ischemic tissue, in order to identify the important key cytokines that promote the survival and angiogenic potency of BMCs.…”
Section: Discussionsupporting
confidence: 78%
“…[2][3][4] However, therapeutic efficacy of this approach for treating post-MI chronic heart failure (HF) has not been fully established. [5][6][7][8][9][10][11] In addition, arrhythmia occurrence, which has been identified as a critical complication of skeletal myoblast injection, 12 has not been fully studied in the case of BM cell injection. Previous clinical studies reported rare incidences of arrhythmia after intramyocardial 5,8,9 and antegrade intracoronary 6,7,10,11 injection of BM cells; however, patients in these studies were prescribed antiarrhythmic drugs such as ␤-blockers, [5][6][7][8][9]11 which could mask arrhythmogenicity of the treatment.…”
mentioning
confidence: 99%
“…In addition, arrhythmia occurrence in these patients might not be adequately examined by appropriate continuous monitoring. 5,[7][8][9][10][11] Elucidating these issues by appropriate laboratory investigations is now an urgent requisite for the further progress of clinical application of the treatment.…”
mentioning
confidence: 99%
“…There also exist a few studies done by using intracoronary infusion method in ischemic cardiomyopathy patients (Kuethe et al 2005;Assmus et al 2007). Cell retention might be expected to be limited after intracoronary delivery into chronically infarcted myocardium, due to the limited blood supply faced by transplanted cells or the environmental factors that affect homing or transdifferentiating into vascular cells and cardiomyocytes.…”
Section: Discussionmentioning
confidence: 99%