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Clinical Characteristics of Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease According to Their Epitopes

Overview
Journal Front Neurol
Specialty Neurology
Date 2023 Jul 12
PMID 37435160
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Abstract

Background: The detection of myelin oligodendrocyte glycoprotein autoantibodies (MOG-Ab) is essential for the diagnosis of MOG-Ab-associated disease (MOGAD). The clinical implications of different epitopes recognized by MOG-Ab are largely unknown. In this study, we established an in-house cell-based immunoassay for detecting MOG-Ab epitopes and examined the clinical characteristics of patients with MOG-Ab according to their epitopes.

Methods: We conducted a retrospective review of patients with MOG-Ab-associated disease (MOGAD) in our single center registry, and collected serum samples from enrolled patients. Human MOG variants were generated to detect epitopes recognized by MOG-Ab. The differences in clinical characteristics according to the presence of reactivity to MOG Proline42 (P42) were evaluated.

Results: Fifty five patients with MOGAD were enrolled. Optic neuritis was the most common presenting syndrome. The P42 position of MOG was a major epitope of MOG-Ab. The patients with a monophasic clinical course and childhood-onset patients were only observed in the group that showed reactivity to the P42 epitope.

Conclusion: We developed an in-house cell-based immunoassay to analyze the epitopes of MOG-Ab. The P42 position of MOG is the primary target of MOG-Ab in Korean patients with MOGAD. Further studies are needed to determine the predictive value of MOG-Ab and its epitopes.

Citing Articles

The MOG antibody non-P42 epitope is predictive of a relapsing course in MOG antibody-associated disease.

Liyanage G, Trewin B, Lopez J, Andersen J, Tea F, Merheb V J Neurol Neurosurg Psychiatry. 2024; 95(6):544-553.

PMID: 38290838 PMC: 11103329. DOI: 10.1136/jnnp-2023-332851.

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