scholarly journals Clinical Trials of Adult Stem Cell Therapy for Peripheral Artery Disease

2013 ◽  
Vol 9 (4) ◽  
pp. 201-205 ◽  
Author(s):  
Crystal M. Botham ◽  
William L. Bennett ◽  
John P. Cooke
2010 ◽  
Vol 55 (10) ◽  
pp. A176.E1654
Author(s):  
Yibin Xie ◽  
Yingli Fu ◽  
Ronald Ouwerkerk ◽  
Steven M. Shea ◽  
Tina Ehtiati ◽  
...  

Cytotherapy ◽  
2013 ◽  
Vol 15 (10) ◽  
pp. 1245-1252 ◽  
Author(s):  
Gábor Viktor Szabó ◽  
Zsuzsa Kövesd ◽  
Judit Cserepes ◽  
Judit Daróczy ◽  
Michael Belkin ◽  
...  

2010 ◽  
Vol 103 (04) ◽  
pp. 696-709 ◽  
Author(s):  
Peter Bramlage ◽  
Berthold Amann ◽  
Holger Lawall

SummaryAtherosclerotic peripheral artery disease (PAD) is a common manifestation of atherosclerosis. The occlusion of large limb arteries leads to ischaemia with claudication which can progress to critical limb ischaemia (CLI) with pain at rest, and to tissue loss. At present, common therapy for CLI is either surgical or endovascular revascularisation aimed at improving blood flow to the affected extremity. However, major amputation and death are still frequent complications. Exploring new strategies for revascularisation of ischaemic limbs is thus of major importance. Bone marrow (BM)-derived stem and progenitor cells have been identified as a potential new therapeutic option to induce therapeutic angiogenesis. Encouraging results of preclinical studies have rapidly led to several small clinical trials, in which BM-derived mononuclear cells were administered to patients with limb ischaemia. Clinical benefits were reported from these trials including improvement of ankle-brachial index (ABI), transcutaneous partial pressure of oxygen (TcPO2), re-duction of pain, and decreased need for amputation. Nonetheless, large randomised, placebo-controlled, double-blind studies are necessary and currently ongoing (BONMOT-CLI, JUVENTUS and NCT00498069). Further research relates to the optimal cell type and dosage, the isolation method, the role of colony-stimulating factors, administration route, and the supportive stimulation of cells with reduced functioning due to advanced PAD. Autologous stem cell therapy for ischaemic peripheral disease seems to be a promising new tool for the treatment of severe limb ischaemia. Preliminary evidence has established its safety, feasibility and effectiveness on several important endpoints. Several large endpoints studies are underway to further consolidate this evidence.


2014 ◽  
Vol 36 (3) ◽  
pp. 165-178 ◽  
Author(s):  
Vincenzo Grimaldi ◽  
Concetta Schiano ◽  
Amelia Casamassimi ◽  
Alberto Zullo ◽  
Andrea Soricelli ◽  
...  

Author(s):  
Paul Bates

Purpose: Adult stem cells are among the new methods of approaching the treatment of myocardial tissue damage. The purpose of this review is to clarify misconceptions about stem cell therapy efficacy in clinical trials and provide a thorough understanding of adult stem cells as a future treatment for patients with myocardial infarction. Methods: A comprehensive review of literature was performed analyzing and comparing 12 clinical trials involving the treatment of patients with acute and chronic myocardial infarction. Results: Stem cell treatments carry an excellent safety profile with the ease of one-time dosing, and have shown dramatic functional improvements while reducing the recurrence of myocardial infarction and enhancing quality of life. Important changes with adult stem cell treatments include 1) formation of new cardiomyocytes, 2) sufficient and sustained improvements in cardiac output, 3) increased myocardial contractility, 4) decreased infarct zone diameter, 5) increased left ventricular function, 6) increased exercise ability, and 7) increased coronary perfusion secondary to neovascularization. Conclusion: At this time, based on the current clinical evidence, adult stem cell therapy is in a position to be considered as an optional treatment for patients with acute or chronic myocardial infarction. Adult stem cell therapy is still in experimental stages of development and the continued clinical involvement will provide more evidence to the therapeutic effects of the treatment.


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