Advances in the Treatment of Neuromyelitis Optica Spectrum Disorder

Neurol Clin. 2021 Feb;39(1):35-49. doi: 10.1016/j.ncl.2020.09.003. Epub 2020 Nov 7.

Abstract

Neuromyelitis optica spectrum disorder (NMOSD) is a rare, relapsing-remitting neuroinflammatory disorder of the central nervous system. Advances in the understanding of NMOSD pathogenesis and identification of the NMO-specific pathogenic anti-AQP4 autoantibody have led to the development of highly effective disease-modifying strategies. Five placebo-controlled, randomized trials for NMOSD have been successfully completed as of 2020. These trials support the efficacy of rituximab and tocilizumab and led to the FDA approval of eculizumab, satralizumab and inebilizumab for NMOSD. Our review provides an update on these evidence-based disease-modifying therapies and discussed the treatment of acute relapses in NMOSD.

Keywords: Anti-CD20 therapy; Anti-IL-6 therapy; Complement inhibition; Immunosuppression; Neuromyelitis optica spectrum disorder; Relapses; Treatment.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Humans
  • Immunologic Factors / therapeutic use*
  • Neuromyelitis Optica / drug therapy*
  • Rituximab / therapeutic use

Substances

  • Antibodies, Monoclonal, Humanized
  • Immunologic Factors
  • Rituximab
  • inebilizumab
  • eculizumab
  • tocilizumab
  • satralizumab