Fühlhuber V, Bick S, Kirsten A, Hahn A, Gerriets T, Tschernatsch M, Kaps M, Preissner K T, Blaes F, Altenkämper S
Dept. of Neurology, Justus-Liebig-University, Giessen, Germany.
J Neuroimmunol. 2009 May 29;210(1-2):87-91. doi: 10.1016/j.jneuroim.2009.03.006. Epub 2009 Mar 31.
Childhood opsoclonus-myoclonus syndrome (OMS) occurs idiopathic or, in association with a neuroblastoma, as a paraneoplastic syndrome. Since autoantibodies were identified in some patients, an autoimmune pathogenesis has been suspected. While the newly discovered B-cell activating factors BAFF and APRIL are involved in systemic autoimmune diseases, their association with neuroimmunological diseases is hardly understood. We here investigated the BAFF and APRIL levels in serum and cerebrospinal fluid (CSF) of OMS patients and their correlation with surface-binding autoantibodies. BAFF and APRIL were both determined by ELISA, and autoantibodies to cerebellar granular neurons (CGN) have been investigated by flow cytometry in 17 OMS patients, 16 neuroblastoma (NB) patients, 13 controls and 11 children with inflammatory neurological diseases (IND). BAFF, but no APRIL, was elevated in the CSF of OMS children and IND children. However, in contrast to IND patients, OMS patients did not have a blood-brain-barrier disturbance, indicating that BAFF was produced intrathecally in OMS patients, but not in IND patients. CSF BAFF levels showed a correlation with CSF CGN autoantibodies (r(2)=0.58, p<0.05). These data indicate that an activated B-cell system in the cerebrospinal fluid is involved in the pathogenesis of OMS, and BAFF may be a candidate parameter for the activation of B-cell immune system.
儿童眼阵挛-肌阵挛综合征(OMS)可特发性发生,或作为副肿瘤综合征与神经母细胞瘤相关联。自从在一些患者中发现自身抗体以来,人们怀疑其发病机制为自身免疫性。虽然新发现的B细胞活化因子BAFF和APRIL参与了全身性自身免疫性疾病,但其与神经免疫性疾病的关联却鲜为人知。我们在此研究了OMS患者血清和脑脊液(CSF)中的BAFF和APRIL水平及其与表面结合自身抗体的相关性。通过酶联免疫吸附测定法(ELISA)测定BAFF和APRIL,并采用流式细胞术对17例OMS患者、16例神经母细胞瘤(NB)患者、13例对照者以及11例患有炎症性神经系统疾病(IND)的儿童检测了小脑颗粒神经元(CGN)自身抗体。OMS患儿和IND患儿的脑脊液中BAFF升高,但APRIL未升高。然而,与IND患者不同,OMS患者不存在血脑屏障紊乱,这表明BAFF是在OMS患者的鞘内产生的,而不是在IND患者中产生。脑脊液BAFF水平与脑脊液CGN自身抗体呈相关性(r²=0.58,p<0.05)。这些数据表明,脑脊液中活化的B细胞系统参与了OMS的发病机制,并且BAFF可能是B细胞免疫系统激活的一个候选参数。