4.7 Article

Spectrum of Novel Anti-Central Nervous System Autoantibodies in the Cerebrospinal Fluid of 119 Patients With Schizophreniform and Affective Disorders

期刊

BIOLOGICAL PSYCHIATRY
卷 92, 期 4, 页码 261-274

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2022.02.010

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资金

  1. Berta-Ottenstein-Programme for Advanced Clinician Scientists, Faculty of Medicine, University of Freiburg
  2. German Research Foundation [PR 1274/2-1, PR 1274/3-1, FOR3004, PR 1274/5-1]
  3. Helmholtz Association [HIL-A03]
  4. German Federal Ministry of Education and Research [Connect-Generate 01GM1908D]
  5. Bayer Vital GmbH
  6. Ipsen Pharma GmbH
  7. Novartis
  8. Biogen GmbH
  9. Genzyme
  10. Roche
  11. Eli Lilly
  12. Janssen-Cilag
  13. Shire
  14. Ethiopia
  15. UCB
  16. GlaxoSmithKline
  17. Servier
  18. Janssen
  19. Cyberonics

向作者/读者索取更多资源

The study identified five novel autoantibody-binding patterns on brain tissue of patients with schizophreniform and affective syndromes. Positive findings were more frequently observed in cerebrospinal fluid (CSF) analysis compared to serum analysis. The frequency and spectrum of autoantibodies in these patient groups may be broader than previously thought.
BACKGROUND: Autoimmune psychosis may be caused by well-characterized anti-neuronal autoantibodies, such as those against the NMDA receptor. However, the presence of additional anti-central nervous system (CNS) autoantibodies in these patients has not been systematically assessed. METHODS: Serum and cerebrospinal fluid (CSF) from patients with schizophreniform and affective syndromes were analyzed for immunoglobulin G anti-CNS autoantibodies using tissue-based assays with indirect immunofluorescence on unfixed murine brain tissue as part of an extended routine clinical practice. After an initial assessment of patients with red flags for autoimmune psychosis (n = 30), tissue-based testing was extended to a routine procedure (n = 89). RESULTS: Based on the findings from all 119 patients, anti-CNS immunoglobulin G autoantibodies against brain tissue were detected in 18% (n = 22) of patients (serum 9%, CSF 18%) following five principal patterns: 1) against vascular structures, most likely endothelial cells (serum 3%, CSF 8%); 2) against granule cells in the cerebellum and/or hippocampus (serum 4%, CSF 6%); 3) against myelinated fibers (serum 2%, CSF 2%); 4) against cerebellar Purkinje cells (serum 0%, CSF 2%); and 5) against astrocytes (serum 1%, CSF 1%). The patients with novel anti-CNS autoantibodies showed increased albumin quotients (p =.026) and white matter changes (p =.020) more frequently than those who tested negative for autoantibodies. CONCLUSIONS: The study demonstrates five novel autoantibody-binding patterns on brain tissue of patients with schizophreniform and affective syndromes. CSF yielded positive findings more frequently than serum analysis. The frequency and spectrum of autoantibodies in these patient groups may be broader than previously thought.

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