ORIGINAL RESEARCH article
Front. Neurol.
Sec. Multiple Sclerosis and Neuroimmunology
Volume 16 - 2025 | doi: 10.3389/fneur.2025.1593042
Autoantibodies against myelin oligodendrocyte glycoprotein in a subgroup of patients with psychotic symptoms
Provisionally accepted- 1Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands, Netherlands
- 2Departments of Neurology, Biomedicine, and Clinical Research and Research Center for Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital of Basel, Basel, Basel-Stadt, Switzerland
- 3Departments of Neurology, Biomedicine, and Clinical Research, and Research Center for Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital of Basel, Basel, Basel-Stadt, Switzerland
- 4Institut de Neuropsiquiatria i Addiccions (INAD), Barcelona, Catalonia, Spain
- 5Centro de Investigación Biomédica en Red, Área de Salud Mental (CIBERSAM), Spain, Madrid, Spain
- 6Department of Neurology, Maastricht University Medical Centre, Maastricht, Netherlands, Netherlands
- 7Department of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Türkiye
- 8Algarve Biomedical Center Research Institute, University of Algarve, Faro, Faro, Portugal
- 9Faculty of Medicine and Biomedical Sciences, University of Algarve, Faro, Faro, Portugal
- 10Department of Child and Adolescent Psychiatry, Hospital General Universitario, Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid, Spain
- 11Department of Psychiatry, Erasmus Medical Center, Rotterdam, Netherlands
- 12Department of Neuroscience, Erasmus Medical Center, Rotterdam, Netherlands
- 13Departments of Neurology, Biomedicine, and Clinical Research, and Research Center for Neuroimmunology and Neuroscience Basel (RC2NB), University of Basel, Basel, Switzerland
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The presence of autoantibodies against myelin oligodendrocyte glycoprotein (MOG) is a hallmark of MOG antibody-associated disease (MOGAD), a recently defined demyelinating disease entity presenting with core clinical features of optic neuritis, myelitis, and acute disseminated encephalomyelitis. Although MOG antibodies have also been described in a small number of patients with other conditions, including mental disorders, their prevalence and clinical specificity in patients with isolated psychotic symptoms remain unclear. We screened sera from 262 patients with at least one psychotic episode and 166 control subjects for the presence of MOG antibodies of the immunoglobulin G (IgG) isotype with a live cell-based assay.Serum reactivity to additional antigens was assessed by immunohistochemistry. Four patients, representing 1.5% of the patient cohort, and one control individual, representing. 0.6% of the healthy control cohort, were seropositive for MOG-IgG antibodies. Of the four MOG-IgG seropositive patients, three experienced visual hallucinations. Overall, MOG antibodies were detected at a low frequency in patients with psychotic episodes. While we cannot exclude the possibility of false-positive results or seroconversion due to secondary myelin damage, the association with visual hallucinations in three out of four MOG-IgG seropositive patients may point toward an underlying autoimmune etiology.
Keywords: myelin oligodendrocyte glycoprotein, Autoantibodies, Neuroinflammation, Psychiatry, Mental Disorders, psychosis Glossary
Received: 13 Mar 2025; Accepted: 02 Jun 2025.
Copyright: © 2025 van de Burgt, Kulsvehagen, Mané Damas, Lutz, Lecourt, Montserrat, Vinke, Küçükali, Zong, Correia-Hoffmann, González-Vioque, Arango, Leibold, Losen, Molenaar, Tüzün, van Beveren, Santacana, Rouhl, Van Amelsvoort, Pröbstel and Martinez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Anne-Katrin Pröbstel, Departments of Neurology, Biomedicine, and Clinical Research, and Research Center for Neuroimmunology and Neuroscience Basel (RC2NB), University of Basel, Basel, 4001, Switzerland
Pilar Martinez, Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, 6226 NB, Netherlands, Netherlands
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