Update on aquaporin-4 antibody detection: the early diagnosis of neuromyelitis optica spectrum disorders

Mult Scler Relat Disord. 2024 Oct:90:105803. doi: 10.1016/j.msard.2024.105803. Epub 2024 Aug 5.

Abstract

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.

Keywords: Aquaporin-4 antibodies; Biosensor; Immunodot; NMO spectrum disorders; NMO-IgG; Neuromyelitis optica.

Publication types

  • Review

MeSH terms

  • Aquaporin 4* / immunology
  • Autoantibodies* / blood
  • Biomarkers / blood
  • Early Diagnosis*
  • Humans
  • Neuromyelitis Optica* / blood
  • Neuromyelitis Optica* / diagnosis
  • Neuromyelitis Optica* / immunology

Substances

  • Aquaporin 4
  • Autoantibodies
  • AQP4 protein, human
  • Biomarkers