Stem cells in patients with heart failure experience
Main Article Content
Abstract
Between 2003 and 2011, 17 patients with heart failure were treated with stem cells as part of our Foundation’s Regenerative Medicine program. In several centers and countries 4 with ischemic cardiomyopathy of which 3 were surgically implanted with autologous bone marrow stem cells (ABMSC) plus bypass surgery. One patient was treated with hyperbaric medicine plus bypass surgery. Patients with idiopathic cardiomyopathy were implanted surgically with 2 different types of stem cells. Ten patients were implanted with stem cells derived from human fetuses (HFDSCs) and three patients with autologous bone marrow stem cells (ABMSC). The ejection fractions of the coronary artery bypass graft off pump OPCAB (control group) versus coronary artery bypass group off pump OPCAB plus stem cell transplantation were as followsin the entire serie: preoperative, 30.7% +/- 2.5% compared to 29.4% +/- 3.6%; 1 month, 36.4% +/- 2.6% versus 42.1% +/- 3.5%; 3 months, 36.5% +/- 3.0% vs. 45.5% +/- 2.2%; And 6 months, 37.2% +/- 3.4% versus 46.1% +/- 1.9% (p <0.001). The first patient performed at our center in Argentina in this series is alive and asymptomatic 15 years after implantation, and the rest of this series we do not have current data. A patient without visible vessels in the anterior wall of the left ventricle was treated with 18 hyperbaric chamber sections from one hour at 1.4 AT. After creating angiogenesis, the patient was operated on receiving 2 grafts (mammary and venous) without extracorporeal circulation in the anterior descending artery and diagonal artery. The preoperative ejection fraction was 33% at 90 months of follow up the ejection fraction was 58%. The patient at 90 months was asymptomatic. Of the idiopathic heart disease group, nine patients underwent median sternotomy, and received human fetal stem cells (HFDSCs from ectopic pregnancy or spontaneous abortion, three patients received autologous bone marrow stem cells ABMSC) and 1HFDSCs for Minimally Invasive Surgery.
Patients with HFDSC, compared to baseline, improved: The mean (±SD) NYHA class decreased from 3.4 ± 0.5 to 1.33 ± 0.5 (P = 0.001); Mean EF increased 31%, from 26.6% ± 4.0% to 34.8% ± 7.2% (p = 0.005); the yield in ETT increased 291.3%, from 4.25 minutes to 16.63 minutes (128.9% in metabolic equivalents, 2.45 to 5.63) (P <0.0001); the mean LVEDD decreased 15%, from 6.85 ± 0.6cm to 5.80 ± 0.58cm (P <0.001); the mean performance on the 6-minute walk test increased 43.2%, from 251 ± 113.1 seconds to 360 ± 0 seconds (P = 0.01); the mean distance increased 64.4%, from 284.4 ± 144.9m to 468.2 ± 89.8m (P = 0.004); and the mean score in the Minnesota congestive HF test decreased from 71 ± 27.3 to 6 ± 5.9 (p <0.001). Kaplan-Maier’s probability of survival at 40 months was 66%. No rejection or cancer was observed at follow-up, in this series follow-up was discontinued at 4 years. In idiopathic patients receiving autologous cells by Mininvasive technique preoperative NYHA was 3.6 (+/- 0.70) 6 months after receiving stem cell therapy. The mean value of the functional class was 1.9 (+/- 0.90) (p <0.005). ) showing marked clinical improvement. The preimplantation ejection fraction was 28% (+/- 3.6%) and at 6 months 44% (+/- 4.7%) (p <0.005). There was a similar change in ventricular diameters: After 6 months LVESV went from 50mm (+/- 3.3) to 42mm (+/- 4.5) (p <0.05). Two of the three patients in this group received re-synchronization therapy; one died at 10 years and 4 months, another at age 11 and another one alive at 12 years of the implant. More experience should be performed with different techniques and cells to find the appropriate treatment in this type of patients.
Article Details
Copyright (c) 2018 Federico B, et al.

This work is licensed under a Creative Commons Attribution 4.0 International License.
The Journal of Stem Cell Therapy and Transplantation is committed in making it easier for people to share and build upon the work of others while maintaining consistency with the rules of copyright. In order to use the Open Access paradigm to the maximum extent in true terms as free of charge online access along with usage right, we grant usage rights through the use of specific Creative Commons license.
License: Copyright © 2017 - 2025 | Open Access by Journal of Stem Cell Therapy and Transplantation is licensed under a Creative Commons Attribution 4.0 International License. Based on a work at Heighten Science Publications Inc.
With this license, the authors are allowed that after publishing with the journal, they can share their research by posting a free draft copy of their article to any repository or website.
Compliance 'CC BY' license helps in:
Permission to read and download | ✓ |
Permission to display in a repository | ✓ |
Permission to translate | ✓ |
Commercial uses of manuscript | ✓ |
'CC' stands for Creative Commons license. 'BY' symbolizes that users have provided attribution to the creator that the published manuscripts can be used or shared. This license allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author.
Please take in notification that Creative Commons user licenses are non-revocable. We recommend authors to check if their funding body requires a specific license.
Remme WJ, Swedberg K. Task force for the diagnosis and treatment of chronic heart failure, European Society of Cardiology. Guidelines for the diagnosis and treatment of chronic heart failure. European Heart Journal. 2001; 22: 1527-1560. Ref.: https://goo.gl/ENjTdx
Colucci W, Braunwald E. Pathophysiology of Heart Failure, en Heart Disease de Braunwald. 5a Edition. 1997; 360-393.
Enrique V, Carbajal MD, Prakas. Current Diagnosis and Treatment is Cardiology 2nd Ed. Congestive Heart Failure. 2003.
Bolling SF, Pagani FD, Deeb GM. Intermediate-term outcome of mitral reconstruction in cardiomyopathy. J Thorac Cardiovasc Surg. 1998; 115: 381-386. Ref.: https://goo.gl/NiiBfR
Wang JS, Shum D, Galipeau J. Marrow stromal cells for cellular cardiomyoplasty: feasibility and potential clinical advantages. J Thorac Cardiovasc Surg. 2000; 120: 999-1006. Ref.: https://goo.gl/1tNxfM
Rafii S, Lyden D. Therapeutic stem and progenitor cell transplantation for organ vascularization and regeneration. Nat Med. 2003; 9: 702-712. Ref.: https://goo.gl/8D8Qqc
Orlic D, Kassutra J, Chimenti S, Jakoniuk I, Anderson SM, et al. Bone marrow cells regenerate infracted myocardium. Nature. 2001; 410: 701-705. Ref.: https://goo.gl/VDLjv3
Edelberg JM, Tang L, Hattori K, Lyden D, Rafii S. Young adult bone marrow-derived endothelial precursor cells restore aging-impaired cardiac angiogenic function. Circ Res. 2002; 90: E89-E93. Ref.: https://goo.gl/2dmhJe
Shi Q, Rafi S, Wu MH, Wijelath ES, Yu C, et al. Evidence for circulating bone marrow-derived endothelial cells. Blood. 1998; 92: 362-367. Ref.: https://goo.gl/z2fWF3
Sata M, Saiura A, Kunisato A, Tojo A, Okada S, et al. Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. Nat Med. 2002; 8: 403-409. Ref.: https://goo.gl/HnCjtL
Otani A, Kinder K, Ewalt K, Otero FJ, Schimmel P, et al. Bone marrow derived stem cells target retinal astrocytes and can promote or inhibit retinal angiogenesis. Nat Med. 2002; 8: 1004-1010. Ref.: https://goo.gl/sJ98ME
Young PP, Hofling AA, Sands MS. VEGF increases engraftment of bone marrow-derived endothelial progenitor cells (EPCs) into vasculalture of newborn murine recipients. Proc Natl Acad Sci USA. 2002; 99: 11951-11956. Ref.: https://goo.gl/TLhwpp
Heyboer M, Milovanova TN, Wojcik S, Grant W, Chin M, et al. CD34+/CD45-dim stem cell mobilization by hyperbaric oxygen - changes with oxygen dosage. Stem Cell Res. 2014; 12: 638-645. Ref.: https://goo.gl/stqQak
O´Donoghue K, Fisk NM. Fetal stem cells. Best Pract Res Clin Obstet Gynaecol. 2004; 18: 853-875. Ref.: https://goo.gl/WFgYr9
Tsymbalyuk VI, Yaminsky YY. Usage of embryonic nerve tissue transplantation to improve the conductivity of spinal cord after traumatic damage in animals and humans. Transplantology. 2003; 4: 199-201.
Zorin MO, Yurchenko TN, Latyshev DY. Application of cryopreserved suspension of embryonic neural cells in combined treatment of patients with ischemic insults of basal ganglias. Transplantology. 2003; 4:149-50.
Salogub TV. Perspective of embryonic cell transplantation when treating patientswthepileptiform neuralgia of peripheric genesis. Transplantology. 2003; 4: 184-185. Ref.: https://goo.gl/BKqVuR
Grischenko VI, Bobirova LE, DvornekIL,y col. Use of biotechnology in treatment of type I dabetes. Transplantology. 2003; 4:16-9.
Benetti F, Penherrera E, Maldonado T, Vera YD, Subramanian V, et al. Direct Myocardial Implantation of Human Fetal Stem Cells in Heart Failure Patients: Long-term Results. Heart Surg Forum. 2010; 13: Ref.: https://goo.gl/FdnVfw
Benetti F, Viña RF, Patel AN. OPCABG plus simultaneous autologus stem cells implants TCTMD.com. 2003.
Patel AN, Geffner L, Vina RF, Saslavsky J, Kormos R, et al. Surgical treatment for congestive heart failure with autologous adult stem cell transplantation: A prospective randomized study: J Thorac Cardiovasc Surg. 2005; 130: 1631-1638. Ref.: https://goo.gl/XTr3sq
Meerson FZ. The myocardium in hyperfunction, hypertrophy and heart failure. Circ Res. 1969; 25: 1-163 Ref.: https://goo.gl/ebUrEX
Zak R. Cardiac hipertrophy: biochemical and cellular relationships. Hosp Pract. 2016; 18: 85-97. Ref.: https://goo.gl/3rKRxD
Prosper F, Pérez A, Merino J. Adult stem cells for myocardial repair. Basic ApplMyol 13(1):15-22,2003.
Colucci WS, Braunwald E. Patophisiology of heart failure in Braunwald¨s Heart Disease 5th edition Saunders company 1997.
Prockop DJ. Marrow Stromal cells as Stem Cells for nonhematopoietic tissues. Science. 1997; 276: 71-74 Ref.: https://goo.gl/m4UcND
Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999; 284: 143-147. Ref.: https://goo.gl/UcXFMi
Makino S, Fukuda K, Miyoshi S, Konishi F, Kodama H, et al. Cardiomyocites can be generated from marrow stromal cells in vitro. J Clin Invest. 1999; 103: 697-705. Ref.: https://goo.gl/N4GYGu
Xu M, Wani M, Dai YS, Wang J, Yan M, et al. Differentiation of bone marrow stromal cells into cardiac phenotype requires intracellular communication with myocites. Circulation 2004; 110: 2658-2665. Ref.: https://goo.gl/kQKnXu
Chedrawy EG, Wang JS, Nguyen DM, Shum-Tim D, Chiu R. Incorporation and integration of implanted myogenic and stem cells into native myocardial fibres: anatomic basis for functional improvements. J Thorac Cardiovasc Surg. 2002; 124: 584-590 Ref.: https://goo.gl/wnW8fH
Pittenger MF, Martin BJ. Mesenchymal stem cells and their potential as cardiac therapeutics. Circulation research. 2004; 95: 9-20 Ref.: https://goo.gl/MQHvLH
Vilas-Boas F, Feitosa GS, Soares MB, Pinho-Filho JA, Mota A, et al. Bone marrow cell transplantation to the myocardium of a patient with heart failure due to Chagas disease. Arg Bras Cardiol. 2004; 82: 181-184. Ref.: https://goo.gl/72WixZ