Agnieshka M Agasing, Saurabh Gawde, Gaurav Kumar, Emma Turner, Robert C Axtell
Journal of neuroimmunology 2020 Jan 15Recent studies identified that interferon beta (IFN-β) treatment skews B-cells towards a regulatory phenotype in multiple sclerosis. To assess B cell involvement during IFN-β therapy, we compared IFN-β treatment in a B cell-independent model and a B cell-dependent model of experimental autoimmune encephalomyelitis (EAE). We show that in B cell-independent EAE, IFN-β ameliorates neuroinflammation. Conversely, in B cell-dependent EAE, IFN-β has no effect on disease. Effective IFN-β therapy in B cell-independent EAE was associated with reduced inflammatory T cells in the CNS and skewed splenic B cells towards an immature population and away from a germinal center population. These immune cell populations were unchanged in B cell-dependent EAE. Finally, we found that IFN-β increased marginal zone B cells in both EAE models. These findings indicate that B cell function impacts IFN-β efficacy during neuroinflammation. Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.
Agnieshka M Agasing, Saurabh Gawde, Gaurav Kumar, Emma Turner, Robert C Axtell. B cell function impacts the efficacy of IFN-β therapy in EAE. Journal of neuroimmunology. 2020 Jan 15;338:577106
PMID: 31715458
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