stem cells for the failing heartnew modalities for hf treatment stem cell therapy - potentially...
TRANSCRIPT
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Zeljko J. Bosnjak, PhD, FAHAProfessor and Vice Chairman for Research
Departments of Anesthesiology and Physiology
The Medical College of Wisconsin, Milwaukee
3rd DUBROVNIK CARDIOLOGY HIGHLIGHTS
Stem Cells for the Failing Heart
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New modalities for HF treatment
Stem cell therapy - potentially disease modifying
Individual clinical studies
Meta-analyses
Future directions and likely outcomes
OVERVIEW
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The management of HF has extended the lifespan of this patient population; however, not able to reverse the disease
Short of heart transplantation, there are currently limited options to overcome the poor prognosis of end-stage HF
This urgent clinical need drives the exploration of cardiac repair with stem cells
Many efforts aim to use the regenerative properties of stem cells for strategies to repair injured myocardium
New modalities for HF treatment
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For nearly a century, the heart has been considered a terminally-differentiated post-mitotic organ unable to replace dying cardiomyocytes
This premise is no longer valid
Pool of resident cardiac stem cells (CSCs) that can acquire the cardiomyocyte, vascular smooth muscle, and endothelial cell lineages has been identified in the human heart
New modalities for HF treatment
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Leri A et al. Circulation Research 2011;109:941-961
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Science. 2009 April 3; 324(5923): 98–102
Birth date of cardiac cells
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The role of hCSCs in restoring damaged myocardium
Spontaneous cardiac repair is minimal; regenerative response to the non-infarcted tissue
Spontaneous myocyte regeneration does not compensate for the loss of myocytes in the chronically pressure-overloaded heart
Spontaneous cardiac repair may delay, but does not avoid or reverse the progression of HF
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Sanganalmath S, Bolli R. Circulation Research 2013;113:810-834
Sources of stem cells for cardiac regeneration and
potential reparative mechanisms
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Implantation of stem cells
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Potential mechanisms of action of stem cells
Sanganalmath S, Bolli R. Circulation Research 2013;113:810-834
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Implantation of stem cells
Most transferred cells are dead within a week
Difficult for cells to engraft, survive, proliferate, and differentiate
Clinical trials demonstrate that autologous cell based therapies for cardiovascular repair are feasible and safe
Although efficacy of cell-based therapy has been limited, it holds enormous promise at preventing or reversing myocardial remodeling and promoting tissue regeneration
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342 studies examining the effects of MSCs
160 studies examining the effects of MSCs in heart failure
http://clinicaltrials.gov (September 2013)
Clinical studies using MSCs
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Use of various types of stem cell therapies in patients with cardiovascular disease
Sanganalmath S, Bolli R. Circulation Research 2013;113:810-834
ALCADIACADUCEUSSCIPIO
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Trials with Negative results:
Late-TIME, Transplantation in Myocardial Infarction Evaluation Cardiovascular Cell Therapy Research Network [CCTRN] TIME
Trials with Positive results:
Percutaneous Stem Cell Injection Delivery Effects on Neomyogenesis (POSEIDON)
Cardiac Stem Cells in Patients with Ischemic Cardiomyopathy (SCIPIO)
Cardiosphere-derived Autologous Stem Cells to Reverse Ventricular Dysfunction (CADUCEUS)
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Open label, non-randomized, prospective study
Intracoronary BMC therapy improves ventricular performance, quality of life, and survival in patients with heart failure
These effects were present when BMC were administered in addition to standard therapeutic regimes
No side effects were observed
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Eur J Fail. 2010 Jul;12(7):721-9.
STAR-heart study
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JAMA. 2013 Aug 21;310(7):750
Phase 1/2 randomized comparison with 13-month follow-up (n=30)
Absence of significant alloimmune reactions in patients receiving allogeneic MSCs
Cell therapy may not only improve left ventricular structure but may also improve quality of life and functional capacity
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JAMA. 2013 Aug 21;310(7):750
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JAMA. 2013 Aug 21;310(7):750
Change in New York Heart Association Classification
Quality of Life
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Lancet 2012; 379: 895–904
Infusion of autologous CDCs after myocardial infarction is safe
Significant increases in viable myocardium is consistent with therapeutic regeneration
No differences in EF or volumes
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Lancet 2012; 379: 895–904
Manufacture of cardiosphere-derived cells
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Lancet 2012; 379: 895–904
CADUCEUS trial changes in scar size
6 months 12 months
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Circulation. 2012;126:S54–S64
CSC infusion produces a striking improvement in both global and regional LV function
Reduction in infarct size
Increase in viable tissue that persist at least 1 year and are consistent with cardiac regeneration
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SCIPIO trial – LVEF
Baseline (27.5 ± 1.6%) 4 months after CSC infusion (35.1 ± 2.4%), 12 months after CSC infusion (41.2 ± 4.5%).
Circulation. 2012;126:S54–S64
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Intracoronary BMSC therapy post-STEMI improves LVEF beyond standard medical treatment, in both the short and longer term
Meta-analysis of 29 studies (1830 patients)
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Effect of intracoronary BMSC on LVEF at 3–6 months
Zimmet H et al. Eur J Heart Fail 2012;14:91-105
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Effect of intracoronary BMSC on LVEF at 12–18 months
Zimmet H et al. Eur J Heart Fail 2012;14:91-105
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Meta-analysis of 50 studies (2625 patients)
Improvement of LV function, infarct size, and remodeling in patients with ischemic heart disease compared with standard therapy
Benefits persist during long-term follow-up
Reduction in deaths, recurrent myocardial infarction, and stent thrombosis
Circulation, 126(5):551-568, 2012
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Forest plot of unadjusted difference in mean change in LVEF in patients treated with BMCs compared with control subjects
Jeevanantham V et al. Circulation 2012;126:551-568
Transplantation of BMCs resulted in a 4% increase in mean LVEF
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Forest plot of mean change in infarct scar size in patients treated BMCs compared with control subjects
Jeevanantham V et al. Circulation 2012;126:551-568
Transplantation of BMCs resulted in a 4% decrease in infarct scar size
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Forest plot of mean change in LVESV in patients treated with BMCs compared with control subjects
Jeevanantham V et al. Circulation 2012;126:551-568
Transplantation of BMCs resulted in a 9% decrease in mean LVESV
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Forest plot of mean change in LVEDV in patients treated with BMCs compared with control subjects
Jeevanantham V et al. Circulation 2012;126:551-568
Transplantation of BMCs resulted in a 5% decrease in mean LVEDV
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Cell types used for cardiac repair
Cell type Source Advantages Disadvantages
Bone marrow BM Autologous Pluripotency
Blood Paracrine effects uncertain
Adult cardiac Cardiac Autologous Invasive cardiac
progenitor cells biopsy Differentiate into biopsy
all cardiac Xenogenic anti-
lineages bodies used for
Paracrine effects isolation
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Resolve the issues concerning optimal cell type, factors, dosage,
patient population, and route and timing of administration
Proceed with rigorous, large-scale, rationally designed, and
randomized clinical trials
--------------------------------
Tissue engineering
MicroRNA regulation of cardiac regeneration
Reprogramming the fibroblasts
To improve the outcome of current cell therapy for
cardiac regeneration in the future:
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Approaches to direct cardiac reprogramming
Qian L, Srivastava D. Circulation Research 2013;113:915-921
Adult InjuredHeart
In vivo iCMs
In vitro iCMsCardiac Fibroblasts
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Off-the-shelf products likely in decade or so
Different mixture of cells for patients with recent MI and those with chronic HF
Infused into the coronary arteries for patients with dilated nonischemic cardiomyopathy
Transendocardial injection to patients with major coronary blockages
Cell therapy unlikely a sole treatment for HF, but an important adjunct to other therapeutic approaches, (prolonged LVA, microRNA, and gene therapy)
Likely outcomes in the future
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Thomas E. Starzl MD, PhD
(“The father of modern transplantation”)
“The history of medicine is that what was
inconceivable yesterday and
barely achievable today often becomes
routine tomorrow”
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Thank you
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MicroRNA regulation of cardiac regeneration
Circ Res 2013;112:1412-1414
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Remuscularising the Failing Heart
Myocardial infarction - one billion myocytes dead
Intramyocardial cell injection - over 95% of the cells are lost
Calculated therapeutic cell dose - 20 billion myocytes
Total myocytes number of the heart is 4 billion