Maruyama Naoki, Shigemoto Kazuhiro
Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Rinsho Shinkeigaku. 2007 Nov;47(11):842-4.
Antibodies to acetylcholine receptor (AChR) are major cause of the human autoimmune disease, myasthenia gravis (MG). Additionally, autoantibodies against Muscle-specific kinase (MuSK) were found in a proportion of patients with generalized MG. After the identification of MuSK antibodies in MG patients, laboratory test for measuring antibodies to MuSK is now required to confirm the diagnosis of MG and the clinical treatment as well as AChR antibodies. MuSK is critical to the clustering of AChR and plays multiple roles at neuromuscular junctions (NMJ). However, it has been dispute concerning the pathogenicity of MuSK antibodies in muscle weakness of MG, as the experimental autoimmune MG caused by MuSK antibodies was absent. Here we describe the recent progress to understand the pathogenic roles of MuSK antibodies in muscle weakness of experimental animals induced by MuSK protein.
抗乙酰胆碱受体(AChR)抗体是人类自身免疫性疾病重症肌无力(MG)的主要病因。此外,在一部分全身型MG患者中发现了抗肌肉特异性激酶(MuSK)的自身抗体。在MG患者中发现MuSK抗体后,现在需要进行检测MuSK抗体的实验室检查,以确诊MG并指导临床治疗,就如同检测AChR抗体一样。MuSK对于AChR的聚集至关重要,并在神经肌肉接头(NMJ)发挥多种作用。然而,由于缺乏由MuSK抗体引起的实验性自身免疫性MG,关于MuSK抗体在MG肌无力中的致病性一直存在争议。在此,我们描述了在了解MuSK抗体在由MuSK蛋白诱导的实验动物肌无力中的致病作用方面的最新进展。