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Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
Tzu-Lun Huang1,2, Jia-Kang Wang1,2,3,4,5, Pei-Yao Chang1,2
1Department of Ophthalmology, Far Eastern Memorial Hospital, Banqiao Dist., New Taipei City 220, Taiwan.
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune CNS disease targeting aquaporin-4. Recent advances clarify NMOSD phenotypes, biomarkers, and pathogenesis, guiding new relapse treatments.
Area of Science:
- Neuroimmunology
- Central Nervous System Inflammatory Disorders
Background:
- Neuromyelitis optica spectrum disorder (NMOSD) is a severe autoimmune inflammatory disease of the central nervous system.
- It is characterized by autoantibodies targeting the aquaporin-4 water channel protein on astrocytes.
- Recent research has significantly advanced the understanding of NMOSD's diverse phenotypes, biomarkers, and inflammatory pathways.
Purpose of the Study:
- To provide an updated review of recent studies on Neuromyelitis optica spectrum disorder (NMOSD).
- To cover key aspects including pathophysiology, biomarkers, diagnostic tools, and animal models.
Main Methods:
- Review of recent scientific literature and clinical trial data on NMOSD.
- Analysis of studies focusing on disease mechanisms, biomarkers (cytokines), and diagnostic technologies (OCT).
- Comparison of various animal models used in NMOSD research.
Main Results:
- Identification of distinct NMOSD phenotypes and complex inflammatory cascades.
- Evaluation of serum and cerebrospinal fluid cytokines as potential biomarkers.
- Assessment of ocular coherence tomography (OCT) for clinical utility.
- Comparison of the relevance and limitations of different NMOSD animal models.
Conclusions:
- Significant progress has been made in understanding NMOSD pathogenesis and identifying potential therapeutic targets.
- Biomarkers and advanced imaging like OCT are crucial for diagnosis and monitoring.
- Ongoing research and clinical trials are paving the way for novel treatments for NMOSD relapses.
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