Use of cell-based assays in myasthenia gravis and other antibody-mediated diseases

被引:40
|
作者
Cruz, P. M. Rodriguez
Huda, S.
Lopez-Ruiz, P.
Vincent, A.
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
[2] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DU, England
关键词
Cell based assay; Acetylcholine receptor; MuSK; LRP4; Agrin; ColQ; Seronegative MG; Neuronal surface antibodies; CLUSTERED ACETYLCHOLINE-RECEPTOR; PROTEIN; 4; CLINICAL-FEATURES; MUSK ANTIBODIES; AUTOANTIBODIES; DIAGNOSIS; MULTICENTER; CORTACTIN; RELEVANCE; AGRIN;
D O I
10.1016/j.expneurol.2015.01.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The increasing demand on diagnostic assays that are sensitive and specific for pathogenic antibodies, and the interest in identifying new antigens, prompted the development of cell-based assays for the detection of autoantibodies in myasthenia gravis and other autoimmune disorders. Cell-based assays were initially used to show that clustering the AChR improved the positivity in myasthenia gravis, and similar assays have now been applied to detection of antibodies to neuromuscular junction candidate proteins such as LRP4 and agrin. In addition cellbased assays have been used in the routine detection of antibodies to proteins expressed on the surface of neurons (NMDAR, LGI1, CASPR2, AMPAR, GABA-A/B, GlyR, and DPPX) and glia (AQP4, MOG). Here, we summarize the findings in myasthenia and discuss the advantages, disadvantages and controversial issues of using cellbased assays in the detection of these antibodies, and their relevance to the testing of preclinical models of disease. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:66 / 71
页数:6
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