视神经脊髓炎
医学
多发性硬化
光谱紊乱
水通道蛋白4
自身抗体
免疫学
抗体
病理
精神科
作者
X.G. Ye,Zhengping Huang,M T Li,Shufen Liu,W Q Huang,Abdullahi Mukhtar Sheik Hamud,Lichao Ye,Linyi Li,Shujuan Wu,Jian-long Zhuang,Yanhong Chen,Xiangrong Chen,Shu Min Lin,Xiaofeng Wei,Chunnuan Chen
标识
DOI:10.1016/j.msard.2024.105803
摘要
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune-mediated primary inflammatory myelinopathy of the central nervous system that primarily affects the optic nerve and spinal cord. The aquaporin 4 antibody (AQP4-Ab) is a specific autoantibody marker for NMOSD. Most patients with NMOSD are seropositive for AQP4-Ab, thus aiding physicians in identifying ways to treat NMOSD. AQP4-Ab has been tested in many clinical and laboratory studies, demonstrating effectiveness in diagnosing NMOSD. Recently, novel assays have been developed for the rapid and accurate detection of AQP4-Ab, providing further guidance for the diagnosis and treatment of NMOSD. This article summarizes the importance of rapid and accurate diagnosis for treating NMOSD based on a review of the latest relevant literature. We discussed current challenges and methods for improvement to offer new ideas for exploring rapid and accurate AQP4-Ab detection methods, aiming for early diagnosis of NMOSD.
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