Blaes F, Pike M G, Lang B
Department of Neurology, Justus-Liebig University, Giessen, Germany.
J Neuroimmunol. 2008 Sep 15;201-202:221-6. doi: 10.1016/j.jneuroim.2008.05.033. Epub 2008 Aug 6.
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.
眼阵挛-肌阵挛综合征或舞动眼综合征(OMS/DES)是一种罕见的儿童神经系统疾病,约50%的病例与神经母细胞瘤(NB)相关。我们检测了5例患有(OMS-NB(+))和5例未患NB(OMS-NB(-))的患者血清中的自身抗体。OMS-NB(-) IgG与NB细胞系表面结合,而来自OMS-NB(+)患者以及未患OMS/DES的NB患者的IgG仅与通透细胞结合。OMS-NB(+)和OMS-NB(-)均降低了NB细胞的增殖。我们还报告了1例未患NB的OMS/DES患儿病例,该患儿未经治疗完全康复。发病时血清抗体与表面结合并降低了NB细胞增殖,但9周后患儿无症状时抗体水平下降。这些结果表明,一些OMS/DES患者的血清中含有可能具有致病性的IgG抗体。