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Blood, 15 March 2007, Vol. 109, No. 6, pp. 2643-2548.
Prepublished online as a Blood First Edition Paper on November 21, 2006; DOI 10.1182/blood-2006-07-035766.


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Submitted July 19, 2006
Accepted November 6, 2006

Development of a secondary autoimmune disorder after hematopoietic stem cell transplantation for autoimmune diseases: role of conditioning regimen used?

Yvonne Loh, Yu Oyama, Laisvyde Statkute, Kathleen Quigley, Kimberly Yaung, Elizabeth Gonda, Walter Barr, Borko Jovanovic, Robert Craig, Dusan Stefoski, Bruce Cohen, and Richard K Burt*

Division of Immunotherapy, Northwestern University Feinberg Medical Center, Chicago, IL
Division of Rheumatology, Northwestern University Feinberg Medical Center, Chicago, IL
Dept of Preventative Medicine, Northwestern University Feinberg Medical Center, Chicago, IL
Division of Gastroenterology, Northwestern University Feinberg Medical Center, Chicago, IL
Dept of Neurological Sciences, Rush University Medical Center, Chicago, IL
Dept of Neurology, Northwestern University Feinberg Medical Center, Chicago, IL

* Corresponding author; email: rburt{at}northwestern.edu.

Patients undergoing autologous HSCT (auto-HSCT) for autoimmune disease may have an added propensity to develop a second autoimmune disorder, given the genetic predisposition to autoimmunity. Therefore, we undertook a retrospective analysis of all patients who have undergone auto-HSCT for an autoimmune disease in our institution to determine the occurrence of a second autoimmune disorder and possible risk factors. In all, 155 patients underwent auto-HSCT for various autoimmune diseases, of which 6 manifested a distinct secondary autoimmune disease at a median of 8.5 months (2 to 30 months) after auto-HSCT. Two patients with systemic lupus erythematosus, conditioned with a regimen containing antithymocyte globulin (ATG), developed factor VIII inhibitors with severe bleeding. Four patients (2 with multiple sclerosis, one each with lupus and systemic sclerosis) who received an alemtuzumab-containing conditioning regimen developed autoimmune cytopenias. Among the 155 patients, the frequency of secondary autoimmune complications was 16.0% with alemtuzumab (4/25), 1.9% for ATG (2/102) and 0% for conditioning regimens without lympho-depleting antibodies (0/28)-a difference which was found to be significantly higher with alemtuzumab exposure (p=0.011). In contrast, gender, type of ATG utilized, and CD34-selection of peripheral blood stem cells were not found to be significantly associated with development of a secondary autoimmune disorder.


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