4.6 Article

Evaluation of a Multiparametric Immunofluorescence Assay for Standardization of Neuromyelitis Optica Serology

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PLOS ONE
卷 7, 期 6, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0038896

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资金

  1. Alenia Areonautica S.p.A.
  2. FORB (Fondazione per la Ricerca Biomedica, ONLUS)
  3. Fondazione San Luigi ONLUS
  4. Czech Ministry of Education [MSM 0021620849]
  5. Grant Agency of Charles University [GAUK 132010]
  6. Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS)
  7. Bayer Vital
  8. Merck Serono
  9. Alenia Aeronautica Spa
  10. Euroimmun, Luebeck, Germany
  11. Biogen Idec
  12. Novartis
  13. Roche
  14. Bayer Schering
  15. Sanofi-Aventis

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Background: Neuromyelitis optica (NMO) is a severely disabling autoimmune disorder of the central nervous system, which predominantly affects the optic nerves and spinal cord. In a majority of cases, NMO is associated with antibodies to aquaporin-4 (AQP4) (termed NMO-IgG). Aims: In this study, we evaluated a new multiparametric indirect immunofluorescence (IIF) assay for NMO serology. Methods: Sera from 20 patients with NMO, 41 patients with multiple sclerosis (MS), 30 healthy subjects, and a commercial anti-AQP4 IgG antibody were tested in a commercial composite immunofluorescence assay (Neurology Mosaic 17; Euroimmun, Germany), consisting of five different diagnostic substrates (HEK cells transfected with AQP4, non-transfected HEK cells, primate cerebellum, cerebrum, and optic nerve tissue sections). Results: We identified AQP4 specific and non-specific fluorescence staining patterns and established positivity criteria. Based on these criteria, this kit yielded a high sensitivity (95%) and specificity (100%) for NMO and had a significant positive and negative likelihood ratio (LR+=infinity, LR-=0.05). Moreover, a 100% inter- and intra-laboratory reproducibility was found. Conclusions: The biochip mosaic assay tested in this study is a powerful tool for NMO serology, fast to perform, highly sensitive and specific for NMO, reproducible, and suitable for inter-laboratory standardization as required for multi-centre clinical trials.

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