Evidence map›Paper›PMID 41646853›Full record

ArticleFrontiers in immunology2026

Adolescent autoimmune encephalitis with dual positive anti-Drebrin and anti-mGluR2 antibodies: a case report.

Anran Liu, Jiarui Huang, Jianqiang Zhang, Junqiang Yan

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Anran LiuKey Laboratory of Molecular Neurobiology, The First Affiliated Hospital of He Nan University of Science and Technology, Luoyang, China.
Jiarui HuangMedical Intensive Care Unit (MICU), Department of Internal Medicine, The First Affiliated Hospital of He Nan University of Science and Technology, Luoyang, China.
Jianqiang ZhangMedical Intensive Care Unit (MICU), Department of Internal Medicine, The First Affiliated Hospital of He Nan University of Science and Technology, Luoyang, China.
Junqiang YanKey Laboratory of Molecular Neurobiology, The First Affiliated Hospital of He Nan University of Science and Technology, Luoyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date, no research has reported the coexistence of anti-Drebrin antibody and anti-mGluR2 antibody in patients with autoimmune encephalitis (AE). This study presents the first detailed case of AE with dual positivity for these antibodies, aiming to enrich the database of double antibody-positive AE and provide clinical insights for diagnosis and treatment. We report a 15-year-old male patient whose main clinical manifestations were mental abnormalities and epileptic seizures, accompanied by frequent irritability and rambling speech. Serological and cerebrospinal fluid (CSF) analyses showed positive results for Drebrin and mGluR2 antibodies. The titer of anti-Drebrin antibody was 1:1000 (serum) and 1:1 (CSF), while the titer of anti-mGluR2 antibody was 1:32+ (serum) and 1:1+ (CSF). Based on the clinical manifestations and diagnostic results, the patient was diagnosed with AE, with concurrent positive anti-Drebrin and anti-mGluR2 antibodies in both serum and CSF. Significant improvement was achieved following immunotherapies, including steroid pulse therapy and intravenous immunoglobulin infusion. Readmission one month later for relapse responded well to renewed immunotherapy, and the patient was discharged with marked improvement. No recurrence was observed during follow-up.

Indexed as

AutoantibodiesEncephalitisHashimoto DiseaseNeuropeptidesReceptors, Metabotropic GlutamateAdolescentHumansMaleTreatment OutcomeAutoantibodiesNeuropeptidesReceptors, Metabotropic Glutamateautoimmune encephalitisCase reportdoubleantibodiesDrebrin antibodymGluR2 antibody

Identifiers

PMID41646853
PMCPMC12867771

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