Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, United Kingdom.
Ann N Y Acad Sci. 2012 Dec;1274:92-8. doi: 10.1111/j.1749-6632.2012.06789.x.
We have established cell-based assays for the improved detection of acetylcholine receptor (AChR) and muscle-specific kinase (MuSK) antibodies in myasthenia gravis. This approach has enabled us to demonstrate antibodies to "clustered" AChRs in patients who were previously AChR antibody negative and can also be used to distinguish between adult and fetal AChR antibodies in mothers of babies with arthrogryposis multiplex congenita. We summarize our recent evidence for the pathogenicity of MuSK and clustered AChR antibodies using in vivo models. Cell-based assays are now also being used for the detection of other antibodies, such as those directed to components of the VGKC/CASPR2/LGI1 complex in Morvan's syndrome, and to AQP4 antibodies in neuromyelitis optica; both of these diseases can be associated with MG and sometimes thymoma. The cell-based method is time consuming but has many advantages and may provide a gold standard for the future in the detection of pathogenic autoantibodies in patients with immune-mediated diseases.
我们已经建立了基于细胞的检测方法,用于改善重症肌无力中乙酰胆碱受体(AChR)和肌肉特异性激酶(MuSK)抗体的检测。这种方法使我们能够在先前 AChR 抗体阴性的患者中检测到“聚集”的 AChR 抗体,并且还可用于区分患有先天性多发性关节挛缩症婴儿的母亲体内的成人和胎儿 AChR 抗体。我们总结了使用体内模型证明 MuSK 和聚集的 AChR 抗体的致病性的最新证据。现在也正在使用基于细胞的检测方法来检测其他抗体,例如在莫旺综合征中针对 VGKC/CASPR2/LGI1 复合物成分的抗体,以及在视神经脊髓炎中针对 AQP4 抗体的检测;这两种疾病均可与重症肌无力和胸腺瘤相关。基于细胞的方法耗时,但具有许多优势,并且可能为未来检测免疫介导性疾病患者中的致病性自身抗体提供金标准。