Autoantibodies in childhood opsoclonus-myoclonus syndrome

被引:30
作者
Blaes, F. [1 ]
Pike, M. G. [3 ]
Lang, B. [2 ]
机构
[1] Univ Giessen, Dept Neurol, Giessen, Germany
[2] Univ Oxford, Dept Clin Neurol, Oxford, England
[3] John Radcliffe Hosp, Dept Paediat Neurol, Oxford OX3 9DS, England
关键词
Opsoclonus-myoclonus syndrome; Dancing Eye Syndrome; Neuroblastoma; Autoantibodies; Cell proliferation; Case report;
D O I
10.1016/j.jneuroim.2008.05.033
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Opsoclonus-myoclonus syndrome or Dancing Eye Syndrome (OMS/DES) is a rare neurological disorder of children, which associates with neuroblastoma (NB) in approximately 50% of cases. We examined sera from five patients with (OMS-NB+) and five without NB (OMS-NB-) for autoantibodies. OMS-NB- IgG bound to the surface of a NB cell line, whereas IgG from OMS-NB+ and from NB patients Without OMS/DES bound only to permeabilised. cells. Both OMS-NB+ and OMS-NB- reduced proliferation of NB cells. We also present a case report of a child with OMS/DES without NB who made a complete recovery without treatment. Serum antibodies at presentation bound to the surface and decreased NB cell proliferation but had decreased 9 weeks later when the child was asymptomatic. These results demonstrate that sera from some OMS/DES patients contain IgG antibodies that are potentially pathogenic. (c) 2008 Elsevier B.V All rights reserved.
引用
收藏
页码:221 / 226
页数:6
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