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Neuromyelitis optica (NMO) is a disorder characterized by optic neuritis and by transverse myelitis that is accompanied by spinal cord lesions exceeding three vertebral segments in length. Presence of an immunoglobin G (IgG) antibody that targets epitopes on the extracellular domain of aquaporin-4 (AQP4) is a specific finding in NMO. However, whether finding AQP4 autoantibodies is simply a marker of or actually pathogenic in NMO remains uncertain. In this study, investigators retrospectively analyzed archived sera from eight patients with NMO-spectrum disorders who had been treated with steroids and immunomodulatory agents (mean follow-up, 62 months). The authors correlated titers of AQP4-specific antibodies with clinical course and CD19 ce…