Blockade of IL-6 signaling in neuromyelitis optica

被引:32
|
作者
Araki, Manabu [1 ,2 ]
机构
[1] Natl Ctr Neurol & Psychiat, Multiple Sclerosis Ctr, Tokyo, Japan
[2] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Immunol, Tokyo, Japan
关键词
Aquaporin; 4; Anti-IL-6 receptor monoclonal antibody; Tocilizumab; Neuromyelitis optica spectrum disorders; INTERLEUKIN-6 RECEPTOR BLOCKADE; OPEN-LABEL; DIAGNOSTIC-CRITERIA; AQUAPORIN-4; ANTIBODY; TOCILIZUMAB; RITUXIMAB; PAIN; PATHOGENESIS; DISTINCTION;
D O I
10.1016/j.neuint.2018.10.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuromyelitis optics (NMO) and neuromyelitis optica spectrum disorder (NMOSD) are autoimmune diseases associated with a disease-specific autoantibody directed against the water channel protein aquaporin-4. Standard immunotherapy, immunosuppressive agents, and corticosteroids can prevent acute attacks and maintain remission in most patients with NMOSD. However, there is a strong need for additional options for patients who are refractory to standard treatments. Emerging therapies targeting specific molecules related to the pathogenicity of NMOSD are currently being developed. The review focuses on improving preventive treatments for NMOSD, including ongoing randomized clinical trials using biological drugs targeting CD19 and CD20 on B cells, interleukin-6, and complement protein C5. The anti-IL-6 receptor monoclonal antibody tocilizumab (TCZ), which can block IL-6 signaling, was shown to be highly effective for refractory patients with NMOSD. Notably, TCZ has marked effects on chronic neuropathic pain and general fatigue in patients refractory to standard medications. TCZ is a promising drug for preventing acute attacks in patients with NMOSD.
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页数:6
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