Authors
Ulf Schulze-Topphoff, Michel Varrin-Doyer, Kara Pekarek, Collin M Spencer, Aparna Shetty, Sharon A Sagan, Bruce AC Cree, Raymond A Sobel, Brian T Wipke, Lawrence Steinman, Robert H Scannevin, Scott S Zamvil
Publication date
2016/4/26
Journal
Proceedings of the National Academy of Sciences
Volume
113
Issue
17
Pages
4777-4782
Publisher
National Academy of Sciences
Description
Dimethyl fumarate (DMF) (BG-12, Tecfidera) is a fumaric acid ester (FAE) that was advanced as a multiple sclerosis (MS) therapy largely for potential neuroprotection as it was recognized that FAEs are capable of activating the antioxidative transcription factor nuclear factor (erythroid-derived 2)-like 2 (Nrf2) pathway. However, DMF treatment in randomized controlled MS trials was associated with marked reductions in relapse rate and development of active brain MRI lesions, measures considered to reflect CNS inflammation. Here, we investigated the antiinflammatory contribution of Nrf2 in DMF treatment of the MS model, experimental autoimmune encephalomyelitis (EAE). C57BL/6 wild-type (WT) and Nrf2-deficient (Nrf2−/−) mice were immunized with myelin oligodendrocyte glycoprotein (MOG) peptide 35–55 (p35–55) for EAE induction and treated with oral DMF or vehicle daily. DMF protected WT and Nrf2 …
Total citations
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Scholar articles
U Schulze-Topphoff, M Varrin-Doyer, K Pekarek… - Proceedings of the National Academy of Sciences, 2016