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Updated: May 31, 2026

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients
Published on: April 14, 2014
Current and future treatment approaches for neuromyelitis optica
Nicolas Collongues1, Jérôme de Seze
1Centre d'investigation Clinique, INSERM 002, Nouvel hopital civil, 1 place de l'hopital, BP 426, 67091 Strasbourg cedex, France; Department of Neurology, University Hospitals of Strasbourg, Strasbourg, France.
Neuromyelitis optica (NMO) is distinct from multiple sclerosis (MS). This review focuses on NMO pathophysiology and proposes new immunosuppressive therapeutic strategies for relapse and disease modification.
Area of Science:
- Neuroimmunology
- Central Nervous System Inflammatory Diseases
Background:
- Neuromyelitis optica (NMO) is a CNS inflammatory disorder causing optic neuritis and myelitis.
- NMO was previously considered a form of multiple sclerosis (MS) but is now recognized as distinct.
- NMO is characterized by B-cell involvement and often associated with anti-aquaporin-4 antibodies.
Purpose of the Study:
- To provide an overview of Neuromyelitis Optica (NMO).
- To review existing therapeutic studies for NMO.
- To propose novel therapeutic strategies for both acute relapses and long-term disease modification in NMO.
Main Methods:
- Literature review of therapeutic studies in NMO.
- Analysis of NMO pathophysiology and disease characteristics.
- Synthesis of data to propose new treatment approaches.
Main Results:
- NMO pathophysiology involves necrotizing vasculitis and B-cell activation.
- NMO is significantly less prevalent than MS, limiting clinical trials.
- Emerging evidence supports immunosuppressive over immunomodulatory treatments for NMO.
Conclusions:
- NMO requires distinct therapeutic strategies from MS.
- Immunosuppressive therapies are indicated for NMO management.
- Further research is needed to develop evidence-based treatment guidelines for NMO.
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