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Volume 17, Issue 4, Pages 348-360 (Winter 2005)


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Cell Therapy for Heart Failure—Muscle, Bone Marrow, Blood, and Cardiac-Derived Stem Cells

Harald C. Ott, MD, Bryce H. Davis, BSE, Doris A. Taylor, PhDCorresponding Author Informationemail address

Heart failure (HF) affects a rapidly growing population of patients. Despite improvements in the understanding and therapy of many stages of cardiovascular disease, there has been little progress in treating HF. In the late-stage disease, current options are cardiac transplantation and mechanical support—options that are limited to a small patient collective. The ischemically injured failing heart lacks contractile myocardium, functional vasculature, and electrical integrity, which has made treatment of the underlying injury untenable in the past. Restoring all of these components seems an overwhelming challenge. Yet, the concept of cell therapy—tissue repair by transplantation of stem and progenitor cells—has opened new potential options for patients with heart failure. Skeletal myoblasts, bone marrow, and blood-derived stem cells have all shown considerable myogenic and angiogenic potential in vitro and have rapidly moved from bench to bedside. A number of nonrandomized, non-placebo-controlled safety and feasibility studies have been reported and now double-blinded randomized controlled trials are underway. Despite this rapid clinical pace, the exact mechanisms underlying the functional benefits of different cell types are not well understood. Instead, multiple similar mechanism have been ascribed to virtually every cell type. Thus, while the field is exciting and offers unheralded promise to treat patients with CVD, we must proceed with due diligence and caution. Only a deep understanding of the benefits versus the risks, and the mechanisms involved in cell-mediated cardiac repair, will allow us to design clinically valuable tools and fulfill the potential of this exciting 21st century approach to treating cardiovascular disease.

 Center for Cardiovascular Repair, University of Minnesota, Minneapolis, Minnesota.

 Department of Biomedical Engineering, Duke University, Durham, North Carolina.

 Center for Cardiovascular Repair, University of Minnesota, Minneapolis, Minnesota.

Corresponding Author InformationAddress reprint requests to: Doris A Taylor, PhD, Center for Cardiovascular Repair, University of Minnesota, 312 Church Street SE, NHH 7-105A, Minneapolis MN 55455.

PII: S1043-0679(05)00074-2

doi:10.1053/j.semtcvs.2005.09.004


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