Journal article
Plasmid-encoded proinsulin preserves C-peptide while specifically reducing proinsulin-specific CD8 T cells in type 1 diabetes
BO Roep, N Solvason, PA Gottlieb, JRF Abreu, LC Harrison, GS Eisenbarth, L Yu, M Leviten, WA Hagopian, JB Buse, M Von Herrath, J Quan, RS King, WH Robinson, PJ Utz, H Garren, L Steinman
Science Translational Medicine | AMER ASSOC ADVANCEMENT SCIENCE | Published : 2013
Abstract
In type 1 diabetes (T1D) an intense inflammatory response destroysβcells in the pancreas, where insulin is produced and released. A therapy for T1D that reduces the specific autoimmune response in this disease while leaving the remainder of the immune system intact has long been sought. Proinsulin is a major target of adaptive immunity in T1D. We hypothesized that an engineered DNA plasmid encoding proinsulin (BHT-3021) would preserveβcell function in T1D patients through reduction of insulin-specific T cells. We studied 80 subjects over 18 years of age who were diagnosed with T1D within 5 years. Subjects were randomized 2:1 to receive intramuscular injections of BHT-3021 or BHT-placebo, wee..
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Awarded by National Institute of Diabetes and Digestive and Kidney Diseases
Funding Acknowledgements
Funding: This work was supported by Bayhill Therapeutics.