Regulatory T-Cells Mediate IFN-α-Induced Resistance against Antigen-Induced Arthritis

Front Immunol. 2018 Feb 19:9:285. doi: 10.3389/fimmu.2018.00285. eCollection 2018.

Abstract

Objective: CD4+FoxP3+CD25+ regulatory T-cells (Tregs) are important for preventing tissue destruction. Here, we investigate the role of Tregs for protection against experimental arthritis by IFN-α.

Methods: Arthritis was triggered by intra-articular injection of methylated bovine serum albumin (mBSA) in wild-type mice, Foxp3DTReGFP+/- mice [allowing selective depletion of Tregs by diphtheria toxin (DT)] and CD4-Cre+/- IFNA1R flox/flox mice (devoid of IFNAR signaling in T-cells) earlier immunized with mBSA, with or without treatment with IFN-α or the indoleamine 2,3-dioxygenase (IDO)-metabolite kynurenine. Tregs were depleted in DT-treated Foxp3DTReGFP+/- mice and enumerated by FoxP3 staining. Suppressive capacity of FACS-sorted CD25+highCD4+ Tregs was tested in vivo by adoptive transfer and ex vivo in cocultures with antigen-stimulated CFSE-stained T-responder (CD25-CD4+) cells. IDO was inhibited by 1-methyl tryptophan.

Results: Both control mice and mice devoid of IFNAR-signaling in T helper cells were protected from arthritis by IFN-α. Depletion of Tregs in the arthritis phase, but not at immunization, abolished the protective effect of IFN-α and kynurenine against arthritis. IFN-α increased the number of Tregs in ex vivo cultures upon antigen recall stimulation but not in naïve cells. IFN-α also increased the suppressive capacity of Tregs against mBSA-induced T-responder cell proliferation ex vivo and against arthritis when adoptively transferred. The increased suppressive activity against proliferation conferred by IFN-α was clearly reduced by in vivo inhibition of IDO at immunization, which also abolished the protective effect of IFN-α against arthritis.

Conclusion: By activating IDO during antigen sensitization, IFN-α activates Tregs, which prevent arthritis triggered by antigen rechallenge. This is one way by which IFN-α suppresses inflammation.

Keywords: experimental arthritis; indoleamine 2,3-dioxygenase; interferon-alpha; kynurenine; regulatory T-cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Experimental / immunology*
  • Cells, Cultured
  • Coculture Techniques
  • Diphtheria Toxin / administration & dosage
  • Female
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / antagonists & inhibitors
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism
  • Interferon-alpha / metabolism*
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Kynurenine / administration & dosage
  • Kynurenine / metabolism
  • Lymphocyte Depletion
  • Mice
  • Mice, Knockout
  • Receptor, Interferon alpha-beta / genetics
  • Serum Albumin, Bovine / immunology
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*
  • Tryptophan / analogs & derivatives
  • Tryptophan / pharmacology

Substances

  • Diphtheria Toxin
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Ifnar1 protein, mouse
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Interferon-alpha
  • Interleukin-2 Receptor alpha Subunit
  • Receptor, Interferon alpha-beta
  • Serum Albumin, Bovine
  • Kynurenine
  • Tryptophan
  • 1-methyltryptophan