Prolonged B-cell depletion after rituximab in AQP4-IgG-positive neuromyelitis optica spectrum disorder

J Neuroimmunol. 2021 Sep 15:358:577666. doi: 10.1016/j.jneuroim.2021.577666. Epub 2021 Jul 18.

Abstract

Rituximab (a B-cell depleting monoclonal antibody) is increasingly utilized for treatment of different immune-mediated neurologic disorders, including aquaporin-4-IgG-positive neuromyelitis optica spectrum disorder (AQP4-IgG-NMOSD). After an initial treatment course, the drug is generally reinfused when peripheral blood B-cells levels re-increase >1% (usually after 6-12 months), or at fixed pre-planned 6-month intervals. We describe the unusual case of a 40-year-old woman with AQP4-IgG-NMOSD who showed a prolonged B-cell depletion for nearly five years after a single rituximab reinfusion. In similar rare patients with exceptionally long-lasting B-cell depletion, rituximab reinfusions at fixed pre-planned intervals would result in unnecessary treatment-related risks and health-care expenses.

Keywords: Aquaporin-4; CD19; NMO; NMOSD; Treatment.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Aquaporin 4* / blood
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / metabolism
  • Female
  • Humans
  • Immunoglobulin G* / blood
  • Immunologic Factors / administration & dosage
  • Lymphocyte Depletion / methods*
  • Middle Aged
  • Neuromyelitis Optica / blood
  • Neuromyelitis Optica / drug therapy*
  • Rituximab / administration & dosage*

Substances

  • Aquaporin 4
  • Immunoglobulin G
  • Immunologic Factors
  • Rituximab