Teriflunomide Treatment of Multiple Sclerosis Selectively Modulates CD8 Memory T Cells

Front Immunol. 2021 Oct 5:12:730342. doi: 10.3389/fimmu.2021.730342. eCollection 2021.

Abstract

Background and objectives: Inhibition of de novo pyrimidine synthesis in proliferating T and B lymphocytes by teriflunomide, a pharmacological inhibitor of dihydroorotate dehydrogenase (DHODH), has been shown to be an effective therapy to treat patients with MS in placebo-controlled phase 3 trials. Nevertheless, the underlying mechanism contributing to the efficacy of DHODH inhibition has been only partially elucidated. Here, we aimed to determine the impact of teriflunomide on the immune compartment in a longitudinal high-dimensional follow-up of patients with relapse-remitting MS (RRMS) treated with teriflunomide.

Methods: High-dimensional spectral flow cytometry was used to analyze the phenotype and the function of innate and adaptive immune system of patients with RRMS before and 12 months after teriflunomide treatment. In addition, we assessed the impact of teriflunomide on the migration of memory CD8 T cells in patients with RRMS, and we defined patient immune metabolic profiles.

Results: We found that 12 months of treatment with teriflunomide in patients with RRMS does not affect the B cell or CD4 T cell compartments, including regulatory TREG follicular helper TFH cell and helper TH cell subsets. In contrast, we observed a specific impact of teriflunomide on the CD8 T cell compartment, which was characterized by decreased homeostatic proliferation and reduced production of TNFα and IFNγ. Furthermore, we showed that DHODH inhibition also had a negative impact on the migratory velocity of memory CD8 T cells in patients with RRMS. Finally, we showed that the susceptibility of memory CD8 T cells to DHODH inhibition was not related to impaired metabolism.

Discussion: Overall, these findings demonstrate that the clinical efficacy of teriflunomide results partially in the specific susceptibility of memory CD8 T cells to DHODH inhibition in patients with RRMS and strengthens active roles for these T cells in the pathophysiological process of MS.

Keywords: CD4 T cells; CD8 T cells; memory T cells; migration; multiple sclerosis; teriflunomide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • CD8-Positive T-Lymphocytes / drug effects*
  • CD8-Positive T-Lymphocytes / enzymology
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Crotonates / adverse effects
  • Crotonates / therapeutic use*
  • Dihydroorotate Dehydrogenase / antagonists & inhibitors*
  • Dihydroorotate Dehydrogenase / metabolism
  • Enzyme Inhibitors / adverse effects
  • Enzyme Inhibitors / therapeutic use*
  • Female
  • Humans
  • Hydroxybutyrates / adverse effects
  • Hydroxybutyrates / therapeutic use*
  • Immunologic Memory / drug effects*
  • Immunosuppressive Agents / adverse effects
  • Immunosuppressive Agents / therapeutic use*
  • Interferon-gamma / metabolism
  • Lymphocyte Activation / drug effects
  • Male
  • Memory T Cells / drug effects*
  • Memory T Cells / enzymology
  • Memory T Cells / immunology
  • Multiple Sclerosis, Relapsing-Remitting / diagnosis
  • Multiple Sclerosis, Relapsing-Remitting / drug therapy*
  • Multiple Sclerosis, Relapsing-Remitting / enzymology
  • Multiple Sclerosis, Relapsing-Remitting / immunology
  • Nitriles / adverse effects
  • Nitriles / therapeutic use*
  • Phenotype
  • Time Factors
  • Toluidines / adverse effects
  • Toluidines / therapeutic use*
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Crotonates
  • Dihydroorotate Dehydrogenase
  • Enzyme Inhibitors
  • Hydroxybutyrates
  • IFNG protein, human
  • Immunosuppressive Agents
  • Nitriles
  • TNF protein, human
  • Toluidines
  • Tumor Necrosis Factor-alpha
  • teriflunomide
  • Interferon-gamma