Rituximab induces a transient fluctuation of peripheral and follicular helper T cells in neuromyelitis optica spectrum disorder

J Neuroimmunol. 2023 Sep 15:382:578167. doi: 10.1016/j.jneuroim.2023.578167. Epub 2023 Jul 29.

Abstract

Autoreactive CD4+ helper T cells are implicated in the pathogenesis of neuromyelitis optica spectrum disorder (NMOSD). Both PD-1+CXCR5+CD4+ T follicular helper (Tfh) cells and PD-1+CXCR5-CD4+ T peripheral helper (Tph) cells can contribute to B-cell immune responses and the production of antibodies. Here we show the effect of B-cell depletion with rituximab on the homeostasis of Tfh cells, Tph cells and their subsets in patients with NMOSD. After rituximab treatment, total Tph cells, total Tfh cells, Tph17 cells, Tph17.1 cells, Tph1 cells, and Tfh1 cells tended to decrease at month 1, but gradually increased at month 6 and restored at month 12. Besides, Tph17.1 cells and Tfh17.1 cells were correlated with the proportion of CD19- antibody-secreting cells. Our data suggest that rituximab induced a fluctuation of proinflammatory Tph and Tfh subsets within one year after initiation of the treatment.

Keywords: NMOSD; Rituximab; T helper cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Neuromyelitis Optica* / drug therapy
  • Programmed Cell Death 1 Receptor
  • Rituximab / pharmacology
  • Rituximab / therapeutic use
  • T Follicular Helper Cells
  • T-Lymphocytes, Helper-Inducer

Substances

  • Rituximab
  • Programmed Cell Death 1 Receptor