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Identification of circulating MOG-specific B cells in patients with MOG antibodies

Authors :
Stephan Winklmeier
Atay Vural
Feyza Gül Özbay
Tania Kümpfel
Gunes Esendagli
Asli Kurne
Ramona Gerhards
Edgar Meinl
Miriam Schlüter
Simone Mader
Rana Karabudak
Franziska S. Thaler
Reinhard Hohlfeld
Berin Inan
Caterina Macrini
Melania Spadaro
Vural, Atay (ORCID 0000-0003-3222-874X & YÖK ID 182369)
Winklmeier, Stephan
Schlueter, Miriam
Spadaro, Melania
Thaler, Franziska S.
Gerhards, Ramona
Macrini, Caterina
Mader, Simone A.
Kurne, Asli
Inan, Berin
Karabudak, Rana
Ozbay, Feyza Gul
Esendagli, Gunes
Hohlfeld, Reinhard
Kuempfel, Tania
Meinl, Edgar
Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
Source :
Neurol Neuroimmunol Neuroinflamm, Neurology: Neuroimmunology and Neuroinflammation, Neurology® Neuroimmunology & Neuroinflammation
Publication Year :
2019
Publisher :
Lippincott Williams & Wilkins, 2019.

Abstract

Objective: to identify circulating myelin oligodendrocyte glycoprotein (MOG)-specific B cells in the blood of patients with MOG antibodies (Abs) and to determine whether circulating MOG-specific B cells are linked to levels and epitope specificity of serum anti-MOG-Abs. Methods: we compared peripheral blood from 21 patients with MOG-Abs and 26 controls for the presence of MOG-specific B cells. We differentiated blood-derived B cells in vitro in separate culture wells to Ab-producing cells via engagement of Toll-like receptors 7 and 8. We quantified the anti-MOG reactivity with a live cell-based assay by flow cytometry. We determined the recognition of MOG epitopes with a panel of mutated variants of MOG. Results: MOG-Ab-positive patients had a higher frequency of MOG-specific B cells in blood than controls, but MOG-specific B cells were only detected in about 60% of these patients. MOG-specific B cells in blood showed no correlation with anti-MOG Ab levels in serum, neither in the whole group nor in the untreated patients. Epitope analysis of MOG-Abs secreted from MOG-specific B cells cultured in different wells revealed an intraindividual heterogeneity of the anti-MOG autoimmunity. Conclusions: This study shows that patients with MOG-Abs greatly differ in the abundance of circulating MOG-specific B cells, which are not linked to levels of MOG-Abs in serum suggesting different sources of MOG-Abs. Identification of MOG-specific B cells in blood could be of future relevance for selecting patients with MOG-Abs for B cell-directed therapy.<br />DFG; Munich Cluster for Systems Neurology EXC 1010 SyNergy and EXC 2145 SyNergy; Clinical Competence Network for Multiple Sclerosis; European Academy of Neurology; Scientific and Technological Research Council of Turkey (TÜBİTAK) 2219 Program; Alexander von Humboldt Foundation; Werner Reichenberger Stiftung; Verein zur Therapieforschung fur Multiple Sklerose-Kranke

Details

Language :
English
Database :
OpenAIRE
Journal :
Neurol Neuroimmunol Neuroinflamm, Neurology: Neuroimmunology and Neuroinflammation, Neurology® Neuroimmunology & Neuroinflammation
Accession number :
edsair.doi.dedup.....aaecdde2f280d8d24e074f9e6964f6dc