Institute of Immunology, Immunity and Infection, University of Glasgow, Glasgow, G12 8TA, UK.
Brain. 2012 Jun;135(Pt 6):1819-33. doi: 10.1093/brain/aws105. Epub 2012 May 4.
Pathological and clinical studies implicate antibody-dependent mechanisms in the immunopathogenesis of multiple sclerosis. We tested this hypothesis directly by investigating the ability of patient-derived immunoglobulins to mediate demyelination and axonal injury in vitro. Using a myelinating culture system, we developed a sensitive and reproducible bioassay to detect and quantify these effects and applied this to investigate the pathogenic potential of immunoglobulin G preparations obtained from patients with multiple sclerosis (n = 37), other neurological diseases (n = 10) and healthy control donors (n = 13). This identified complement-dependent demyelinating immunoglobulin G responses in approximately 30% of patients with multiple sclerosis, which in two cases was accompanied by significant complement-dependent antibody mediated axonal loss. No pathogenic immunoglobulin G responses were detected in patients with other neurological disease or healthy controls, indicating that the presence of these demyelinating/axopathic autoantibodies is specific for a subset of patients with multiple sclerosis. Immunofluorescence microscopy revealed immunoglobulin G preparations with demyelinating activity contained antibodies that specifically decorated the surface of myelinating oligodendrocytes and their contiguous myelin sheaths. No other binding was observed indicating that the response is restricted to autoantigens expressed by terminally differentiated myelinating oligodendrocytes. In conclusion, our study identifies axopathic and/or demyelinating autoantibody responses in a subset of patients with multiple sclerosis. This observation underlines the mechanistic heterogeneity of multiple sclerosis and provides a rational explanation why some patients benefit from antibody depleting treatments.
病理和临床研究表明,抗体依赖性机制参与了多发性硬化症的免疫发病机制。我们通过研究患者来源的免疫球蛋白在体外介导脱髓鞘和轴突损伤的能力,直接检验了这一假说。我们使用髓鞘形成培养系统,开发了一种敏感且可重复的生物测定法来检测和量化这些效应,并应用该方法来研究从多发性硬化症患者(n=37)、其他神经疾病患者(n=10)和健康对照供体(n=13)获得的免疫球蛋白 G 制剂的致病潜力。该方法鉴定了约 30%的多发性硬化症患者存在补体依赖性脱髓鞘免疫球蛋白 G 反应,其中在两种情况下伴有显著的补体依赖性抗体介导的轴突丢失。在其他神经疾病患者或健康对照者中未检测到致病免疫球蛋白 G 反应,表明这些脱髓鞘/轴突病自身抗体的存在是多发性硬化症亚组患者所特有的。免疫荧光显微镜显示具有脱髓鞘活性的免疫球蛋白 G 制剂含有特异性修饰髓鞘形成少突胶质细胞及其连续髓鞘的抗体。未观察到其他结合,表明该反应仅限于终末分化的髓鞘形成少突胶质细胞表达的自身抗原。总之,我们的研究在多发性硬化症的亚组患者中鉴定出了轴突病和/或脱髓鞘自身抗体反应。这一观察结果强调了多发性硬化症的机制异质性,并为一些患者从抗体耗竭治疗中获益提供了合理的解释。