Neuromyelitis optica spectrum disorders - laboratory examination

被引:0
作者
Nytrova, P. [1 ]
Kral, V [2 ]
机构
[1] Neurol Klin & Ctr Klin Neuroved, 1 LF UK & VFN Praze,Katerinska 30, Prague 12808, Czech Republic
[2] Zdravotni Ustav Sidlem Usti nad Labem, Ctr Imunol & Mikrobiol, Usti Nad Labem, Czech Republic
关键词
neuromyelitis optica; MOG encephalomyelitis; antibodies to aquaporin-4; antibodies to myelin oligodendrocyte glycoprotein; cell-based assays; MYELIN OLIGODENDROCYTE GLYCOPROTEIN; MULTIPLE-SCLEROSIS; ANTIBODIES; MARKER; NMO;
D O I
10.14735/amcsnn2020S31
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The assessment of neuronal antibodies improves diagnostic accuracy in a group of autoimmune disorders of the CNS. One of these examples is the detection of autoantibodies to aquaporin-4 (AQP4-IgG) in patients with neuromyelitis optica (NMO). The discovery of these antibodies has improved understanding of the pathogenesis and therapeutic approach in this syndrome. Furthermore, these antibodies facilitated the differentiation between NMO and MS. The sensitivity and specificity of these antibodies increased thanks to the assessment using cell-based assays in which antigen is expressed as a native protein in a membrane of the transfected cell. This was confirmed by testing of other antibodies targeting myelin oligodendrocyte glycoprotein, which are associated with acute disseminated encephalomyelitis or AQP4-IgGnegNMO. These autoantibodies are rarely detected in patients with MS.
引用
收藏
页码:S31 / S36
页数:6
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