Stich O, Rauer S
Neurologische Klinik und Poliklinik der Albert-Ludwigs-Universitaet Freiburg, Freiburg, Germany.
Eur J Neurol. 2007 Jun;14(6):650-3. doi: 10.1111/j.1468-1331.2007.01802.x.
Using isoelectric focusing and affinity blotting employing paraneoplastic recombinant antigens, we investigated cerebrospinal fluid (CSF) and sera from three patients with positive anti-CV2/CRMP5- and one patient with positive anti-amphiphysin serology. CSF and sera were previously adjusted to total IgG concentrations of 20 mg/l. All patients suffered from paraneoplastic neurological syndromes (PNS) with predominant involvement of the central nervous system (CNS). Using affinity blot preloaded with paraneoplastic antigen, we detected in three of four patients more or stronger specific oligoclonal bands (OCB) in the CSF than in the corresponding serum, providing qualitative evidence of antigen specific intrathecal antibody synthesis. These results are in line with previous studies demonstrating specific OCB predominantly in CSF from patients with anti-Hu-, anti-Yo- and anti-Ri-associated PNS, supporting the hypothesis of autoimmunity in the pathogenesis of PNS. One patient harboured extensive anti-amphiphysin specific OCB, although OCB of total IgG could not be detected, indicating a higher sensitivity for detection of intrathecal antibody synthesis of the affinity blot preloaded with the paraneoplastic antigen, compared with investigation of total IgG OCB. These results could have implications concerning pathophysiological autoimmune aspects in other inflammatory diseases of CNS associated with total IgG OCB, provided that the target antigen is known.
利用等电聚焦和采用副肿瘤重组抗原的亲和印迹法,我们研究了3例抗CV2/CRMP5抗体阳性患者和1例抗 amphiphysin 抗体血清学阳性患者的脑脊液(CSF)和血清。CSF和血清先前已调整至总IgG浓度为20mg/l。所有患者均患有以中枢神经系统(CNS)为主受累的副肿瘤性神经系统综合征(PNS)。使用预加载副肿瘤抗原的亲和印迹法,我们在4例患者中的3例中检测到CSF中比相应血清中更多或更强的特异性寡克隆带(OCB),为抗原特异性鞘内抗体合成提供了定性证据。这些结果与先前的研究一致,先前研究表明抗Hu、抗Yo和抗Ri相关PNS患者的CSF中主要存在特异性OCB,支持PNS发病机制中的自身免疫假说。1例患者存在广泛的抗 amphiphysin 特异性OCB,尽管未检测到总IgG的OCB,这表明与检测总IgG OCB相比,预加载副肿瘤抗原的亲和印迹法检测鞘内抗体合成的敏感性更高。如果已知靶抗原,这些结果可能对与总IgG OCB相关的其他中枢神经系统炎症性疾病的病理生理自身免疫方面有影响。