Tofacitinib inhibits the development of experimental autoimmune uveitis and reduces the proportions of Th1 but not of Th17 cells

Mol Vis. 2020 Sep 26:26:641-651. eCollection 2020.

Abstract

Purpose: Tofacitinib is a pan-Janus kinase (JAK) inhibitor that suppresses cytokine signaling and in turn, the cells that participate in inflammatory immunopathogenic processes. We examined the capacity of tofacitinib to inhibit the induction of experimental autoimmune uveitis (EAU) and related immune responses.

Methods: EAU was induced in B10.A mice with immunization with bovine interphotoreceptor retinoid-binding protein (IRBP), emulsified in complete Freund's adjuvant (CFA), and a simultaneous injection of pertussis toxin. Tofacitinib, 25 mg/kg, was administered daily, and the vehicle was used for control. EAU development was assessed by histological analysis of the mouse eyes, and related immune responses were assessed by (i) the levels of interferon (IFN)-γ and interleukin (IL)-17, secreted by spleen cells cultured with IRBP; (ii) flow cytometric analysis of intracellular expression by spleen, or eye-infiltrating CD4 or CD8 cells of IFN-γ, IL-17, and their transcription factors, T-bet and RORγt. In addition, the inflammation-related cell markers CD44 and CD62L and Ki67, a proliferation marker, were tested. The proportions of T-regulatory cells expressing FoxP3 were determined by flow cytometric intracellular staining, while levels of antibody to IRBP were measured with enzyme-linked immunosorbent assay (ELISA).

Results: Treatment with tofacitinib significantly suppressed the development of EAU and reduced the levels of secreted IFN-γ, but not of IL-17. Further, treatment with tofacitinib reduced in the spleen and eye-infiltrating cells the intracellular expression of IFN-γ and its transcription factor T-bet. In contrast, treatment with tofacitinib had essentially no effect on the intracellular expression of IL-17 and its transcription factor, RORγt. The selective effect of tofacitinib treatment was particularly evident in the CD8 population. Treatment with tofacitinib also increased the population of CD44, but reduced the populations of cells producing CD62L and Ki67. Treatment with tofacitinib had no effect on the proportion of FoxP3 producing regulatory cells and on the antibody production to IRBP.

Conclusions: Treatment with tofacitinib inhibited the development of EAU, reduced the production of IFN-γ, but had essentially no effect on the production of IL-17.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • CD4 Antigens / blood
  • CD4-Positive T-Lymphocytes / drug effects
  • CD4-Positive T-Lymphocytes / immunology
  • CD8 Antigens / blood
  • CD8-Positive T-Lymphocytes / drug effects
  • CD8-Positive T-Lymphocytes / immunology
  • Eye / drug effects
  • Eye / metabolism*
  • Eye / pathology
  • Eye Proteins / pharmacology
  • Forkhead Transcription Factors / blood
  • Hyaluronan Receptors / blood
  • Immunosuppression Therapy
  • Interferon-gamma / blood
  • Interleukin-17 / blood
  • Ki-67 Antigen / blood
  • L-Selectin / blood
  • Mice
  • Piperidines / administration & dosage
  • Piperidines / pharmacology*
  • Pyrimidines / administration & dosage
  • Pyrimidines / pharmacology*
  • Retinol-Binding Proteins / pharmacology
  • Th1 Cells / drug effects*
  • Th1 Cells / immunology
  • Th17 Cells / drug effects*
  • Th17 Cells / immunology
  • Uveitis / drug therapy*
  • Uveitis / immunology*

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Eye Proteins
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Hyaluronan Receptors
  • Il17a protein, mouse
  • Interleukin-17
  • Ki-67 Antigen
  • Piperidines
  • Pyrimidines
  • Retinol-Binding Proteins
  • interstitial retinol-binding protein
  • L-Selectin
  • Interferon-gamma
  • tofacitinib