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Reversal of Diabetes in Non-Obese Diabetic Mice Without Spleen Cell-Derived ß Cell Regeneration
Anita S. Chong,1*Jikun Shen,1Jing Tao,1Dengping Yin,1,3Andrey Kuznetsov,2Manami Hara,2Louis H. Philipson2
Autoimmune destruction of ß cells is the predominantcause of type 1 diabetes mellitus (T1DM) in humans and is modeledin non-obese diabetic (NOD) mice. Many therapeutic interventionsprevent the development of T1DM in NOD mice, but few can induceits reversal once established. Intervention with Freund's completeadjuvant, semi-allogeneic splenocytes, and temporary islet transplantationhas been reported to cure NOD mice of established T1DM. Usingthe same approach, we report here that this treatment cured32% of NOD mice of established diabetes (>340 milligramsper deciliter blood glucose), although ß cells inthese mice were not derived from donor splenocytes.
1 Section of Transplantation, Department of Surgery, The University of Chicago, Chicago, IL 60637, USA. 2 Section of Endocrinology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA. 3 Department of Surgery, University of Illinois at Chicago, Chicago, IL 60612, USA.
* To whom correspondence should be addressed. E-mail: achong{at}uchicago.edu
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