Abstract
Critical limb ischemia (CLI) is an advanced form of peripheral artery disease which is responsible for approximately 100,000 amputations per year in the US. Trials to date have reported clinical improvement and reduced need for amputation in CLI patients receiving autologous bone marrow or mobilized peripheral blood stem cells for stimulation of angiogenesis. While such treatments are currently entering Phase III trials, practical and scientific pitfalls will limit widespread implementation if efficacy is proven. Hurdles to be overcome include: a) reduced angiogenic potential of autologous cells in aged patients with cardiovascular risk factors; b) invasiveness/adverse effects of bone marrow extraction and G-CSF mobilization, respectively; and c) need for on-site cellular manipulation. The Endometrial Regenerative Cell (ERC) is a mesenchymal-like stem cell derived from the menstrual blood that is believed to be associated with endometrial angiogenesis. We discuss the possibility of using allogeneic ERCs as an "off the shelf" treatment for CLI based on the following properties: a) High levels of growth factors and matrix metalloprotease production; b) Ability to inhibits inflammatory responses and lack of immunogenicity; and c) Expandability to great quantities without loss of differentiation ability or karyotypic abnormalities.
Highlights
Journal of Translational Medicine 2008, 6:45 http://www.translational-medicine.com/content/6/1/45 atherosclerosis or in a smaller number of patients by thromboangiitis obliterans (Buerger's Disease), or arteritis
The dismal state of options for this patient population was best surmised by Schainfeld and Isner in the statement "Critical limb ischemia: nothing to give at the doctors office" [4]
It has been observed that ischemic muscles secrete angiogenic factors in response to hypoxia and that to some extent natural angiogenesis does occur in animal models of CLI and in humans [5,6]
Summary
Journal of Translational Medicine 2008, 6:45 http://www.translational-medicine.com/content/6/1/45 atherosclerosis or in a smaller number of patients by thromboangiitis obliterans (Buerger's Disease), or arteritis. The same study demonstrated that administration of bone marrow cells into muscles of mice with induced hindlimb ischemia led to neoangiogenesis mediated in part by the transferred cells [29]. A study using a similar model demonstrated improved perfusion subsequent to bone marrow administration and enhanced production of the angiogenic cytokines IL-1 and FGF-2 [31].
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