Rheumatology Advance Access originally published online on June 15, 2006
Rheumatology 2006 45(10):1187-1193; doi:10.1093/rheumatology/kel158
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Adult stem cells in the treatment of autoimmune diseases
1Department of Rheumatology, Leiden University Medical Center, The Netherlands and 2Department of Rheumatology, Felix-Platter Spital, Basel, Switzerland.
Correspondence to: Alan Tyndall, Department of Rheumatology, University of Basel, Felix Platter Spital, Burgfelderstrasse 101, Basel 4012, Switzerland. E-mail: alan.tyndall{at}fps-basel.ch
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Abstract |
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During the past 10 yrs, over 700 patients suffering from severe autoimmune disease (AD) have received an autologous haematopoietic stem cell transplant as treatment of their disorder with durable remission being obtained in around one-third. The most commonly transplanted ADs have been systemic sclerosis (scleroderma), multiple sclerosis, rheumatoid arthritis, juvenile idiopathic arthritis and systemic lupus erythematosus. A fewer number of patients have received an allogeneic transplant. The initially reported overall treatment-related mortality of 7% has since fallen, with no further cases being reported in systemic sclerosis or multiple sclerosis in the past 3 yrs. This is thought to be due to more careful patient selection.The phase I/II data has led to currently running prospective randomised trials in systemic sclerosis, multiple sclerosis and systemic lupus erythematosus in Europe and North America. Immune reconstitution data suggests a ‘resetting’ of autoimmunity in those patients achieving stable remission, rather than simply prolonged immunosuppression. Recent results from in vitro experiments, animal models and early human experience in severe acute graft vs host disease suggest that multipotent mesenchymal stromal cells obtained from the bone marrow and expanded ex vivo, may exert a clinically useful immunomodulatory effect. Such cells are immune privileged and apparently of low toxicity. Further characterization of these cells and consideration of their possible clinical application in AD is underway.
KEY WORDS: Stem cell, Transplantation, MSC, Autoimmune disease, Scleroderma
Submitted 14 November 2005;
revised version accepted 4 April 2006.
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