Clinical characteristics of MOG antibody-positive anti-NMDAR encephalitis: a single-center retrospective study

Xuan Zou1,2,3,4, Guan-En Zhou1,2,3,4

  • 1Department of Neurology, Tianjin Huanhu Hospital, Tianjin University, Tianjin, China.

Frontiers in Neurology
|February 12, 2026
PubMed
Abstract

Insights

Myelin oligodendrocyte glycoprotein (MOG) antibody-positive anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis presents differently, with higher rates of male patients, headaches, and MRI abnormalities. These patients also face a significantly higher risk of recurrence, suggesting a need for tailored treatment strategies.

Area of Science:

  • Neuroimmunology
  • Neurology
  • Autoimmune Encephalitis

Background:

  • Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is a severe autoimmune neurological disorder.
  • Co-occurrence with myelin oligodendrocyte glycoprotein (MOG) antibodies is rare but may influence clinical presentation and prognosis.
  • Understanding these differences is crucial for accurate diagnosis and effective management.

Purpose of the Study:

  • To elucidate the distinct clinical characteristics of anti-NMDAR encephalitis in patients who are also positive for MOG antibodies (MOG-Ab (+)).
  • To compare the clinical profiles and outcomes of MOG-Ab (+) anti-NMDAR encephalitis patients with those who are MOG-Ab negative (MOG-Ab (-)).

Main Methods:

  • A single-center retrospective study involving 48 patients diagnosed with anti-NMDAR encephalitis.
  • Patients were divided into two groups: MOG-Ab (+) (n=8) and MOG-Ab (-) (n=40).
  • Clinical data, including demographics, symptoms, cerebrospinal fluid (CSF) analysis, MRI findings, and recurrence rates, were collected and statistically analyzed.

Main Results:

  • The MOG-Ab (+) group showed a significantly higher proportion of males (87.5% vs. 40%) and frequent headaches (75% vs. 25%).
  • Elevated CSF white blood cell (WBC) counts (12.5 times higher), increased leptomeningeal enhancement (37.5%), and cortical lesions (87.5%) on MRI were more common in the MOG-Ab (+) group.
  • Recurrence rates within one year were substantially higher in the MOG-Ab (+) group (50% vs. 12.5%).

Conclusions:

  • Testing for MOG antibodies is recommended for anti-NMDAR encephalitis patients with headaches, elevated CSF-WBC, and abnormal MRI findings, especially in male patients.
  • The presence of both MOG and NMDAR antibodies indicates a more severe inflammatory response and a higher risk of recurrence.
  • Aggressive, long-term immunosuppressive therapy may be warranted for patients with dual antibody positivity to prevent disease relapse.

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