Chester K A, Lang B, Gill J, Vincent A, Newsom-Davis J
Department of Neurological Science, Royal Free Hospital School of Medicine, London, U.K.
J Neuroimmunol. 1988 May;18(2):97-104. doi: 10.1016/0165-5728(88)90058-6.
Lambert-Eaton myasthenic syndrome (LEMS) is a paraneoplastic autoimmune disorder caused by an IgG-mediated reduction in number of presynaptic voltage-gated calcium channels (VGCC) at the neuromuscular junction. In at least 50% of cases, the stimulus for antibody production may be VGCC on small cell lung cancer (SCLC). In this study membranes isolated from a human small cell lung cancer xenograft (Mar), that bound [3H]PN200-110, a VGCC antagonist, were subjected to Western blotting using plasma from 12 LEMS patients and eight controls. Although one band recognised by 3/12 LEMS IgGs might be associated with the VGCC, a number of other proteins were recognised both by LEMS plasma, and by plasma from patients with other disorders. The results illustrate the difficulties found using Western blotting with autoimmune plasma to identify specific polypeptides in a crude antigen preparation.
兰伯特-伊顿肌无力综合征(LEMS)是一种副肿瘤性自身免疫性疾病,由IgG介导的神经肌肉接头处突触前电压门控钙通道(VGCC)数量减少所致。至少50%的病例中,抗体产生的刺激因素可能是小细胞肺癌(SCLC)上的VGCC。在本研究中,从人小细胞肺癌异种移植瘤(Mar)分离出的膜,其可结合VGCC拮抗剂[3H]PN200 - 110,使用12例LEMS患者和8例对照的血浆进行蛋白质印迹分析。虽然12份LEMS IgG中有3份识别出的一条带可能与VGCC相关,但许多其他蛋白质既能被LEMS血浆识别,也能被其他疾病患者的血浆识别。结果表明,使用自身免疫性血浆进行蛋白质印迹分析以在粗抗原制剂中鉴定特定多肽存在困难。