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Review Article

Cell therapy in critical limb ischemia: current developments and future progress

, , , , , & show all
Pages 902-916 | Received 06 Oct 2011, Accepted 07 May 2012, Published online: 25 Jun 2012
 

Abstract

Critical limb ischemia (CLI) is a syndrome manifested by ischemic rest pain, non-healing ulcers and tissue loss. CLI patients are at very high risk of amputation and experience poor physical function, leading to severe morbidity and mortality. The fundamental goal for CLI treatment is to relieve ischemic rest pain, heal ulcers, prevent limb loss and improve the quality of life, thereby extending the survival of the patient. Surgical or endovascular revascularization aimed at increasing blood flow is currently available for limb salvage in CLI. However, up to 30% of CLI patients are not suitable for such interventions because of high operative risk or unfavorable vascular anatomy. Therefore exploring new and more effective strategies for revascularization of ischemic limbs is imperative for the establishment of a viable therapeutic alternative. With the emergence of new approaches, this review describes up-to-date progress and developments in cell-based therapy as a novel and promising alternative for CLI treatment. Preliminary clinical data have established the safety, feasibility and efficacy of stem cells, and numerous studies are underway to consolidate this evidence further. However, significant hurdles remain to be addressed before this research can be responsibly translated to the bedside. In particular, we need better understanding of the behavior of cells post-transplantation and to learn how to control their survival and migration proliferation/differentiation in the hostile pathologic environment. Future research should focus on methods of isolation, optimal dosage, appropriate cell type, route of administration, role of tissue-derived factors and supportive endogenous stimulation.

Acknowledgments

The authors are grateful to Stempeutics Research Malaysia for the funding to carry out research on stem cells and regenerative medicine. We also acknowledge the scientific staff of Stempeutics for their support, which helped to improve the manuscript. The authors acknowledge Megan Laycock for careful proofreading of the manuscript.

Author disclosure statement: No competing financial interests exist.

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