Anti-Myelin Oligodendrocyte Glycoprotein Antibodies in Pediatric Patients With Optic Neuritis

作者：Rostasy Kevin^*; Mader Simone; Schanda Kathrin; Huppke Peter; Gaertner Jutta; Kraus Verena; Karenfort Michael; Tibussek Daniel; Blaschek Astrid; Bajer Kornek Barbara; Leitz Steffen; Schimmel Mareike; Di Pauli Franziska; Berger Thomas; Reindl Markus

来源：Archives of Neurology, 2012, 69(6): 752-756.

DOI：10.1001/archneurol.2011.2956

Objective: To study the humoral immune response directed at myelin oligodendrocyte glycoprotein (MOG) in pediatric patients with isolated and recurrent optic neuritis (ON). %26lt;br%26gt;Design: Observational prospective case series. %26lt;br%26gt;Setting: Six pediatric hospitals in Germany and Austria. %26lt;br%26gt;Patients: Thirty-seven patients 18 years or younger with single or recurrent episodes of ON were recruited from 6 different hospitals. %26lt;br%26gt;Main Outcome Measures: Clinical features, magnetic resonance imaging findings, intrathecal IgG synthesis, and outcome were recorded. A live cell-based immunofluorescence assay was used to measure serum IgG antibodies to MOG and aquaporin 4. %26lt;br%26gt;Results: A single episode of ON was observed in 10 patients, and 15 experienced 2 to 12 episodes. The acute episode of ON was part of a clinically isolated syndrome in 12 patients, of whom 8 were subsequently classified as having multiple sclerosis. High-titer serum MOG-IgG antibodies (%26gt;= 1:160) were detected in 17 patients (46%). In addition, high titers of MOG-IgG antibodies were more frequently observed in 12 of the 15 patients with recurrent episodes of ON (80%; median titer, 1:640) compared with 2 of the 10 patients with monophasic ON (20%; median titer, 0) and 3 of the 12 patients with ON as part of a clinically isolated syndrome (25%; median titer, 0). %26lt;br%26gt;Conclusion: High-titer MOG-IgG antibodies are predominantly detected in pediatric patients with recurrent ON, indicating that anti-MOG-specific antibodies may exert a direct role in the pathogenesis of ON in this subgroup. Arch Neurol. 2012; 69(6): 752-756. Published online February 27, 2012. doi:10.1001/archneurol.2011.2956

• 出版日期2012-6