Epithelial cell-derived CD83 restores immune tolerance in the airway mucosa by inducing regulatory T-cell differentiation

Immunology. 2021 Jul;163(3):310-322. doi: 10.1111/imm.13317. Epub 2021 Feb 28.

Abstract

The mechanism of generation of regulatory T cells (Treg) remains incompletely understood. Recent studies show that CD83 has immune regulatory functions. This study aims to investigate the role of epithelial cell-derived CD83 in the restoration of immune tolerance in the airway mucosa by inducing the Treg differentiation. In this study, CD83 and ovalbumin (OVA)-carrying exosomes were generated from airway epithelial cells. An airway allergy mouse model was developed to test the role of CD83/OVA-carrying exosomes in the suppression of airway allergy by inducing Treg generation. We observed that mouse airway epithelial cells expressed CD83 that could be up-regulated by CD40 ligand. The CD83 deficiency in epithelial cells retarded the Treg generation in the airway mucosa. CD83 up-regulated transforming growth factor-β-inducible early gene 1 expression in CD4+ T cells to promote Foxp3 expression. Exposure of primed CD4+ T cells to CD83/OVA-carrying exosomes promoted antigen-specific Treg generation. Administration of CD83/OVA-carrying exosomes inhibited experimental airway allergic response. In summary, airway epithelial cells express CD83 that is required in the Treg differentiation in the airway mucosa. Administration of CD83/OVA-carrying exosomes can inhibit airway allergy that has the translation potential in the treatment of airway allergic disorders.

Keywords: CD83; airway mucosa; epithelial cell; immune tolerance; mucosal immunology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / immunology
  • Animals
  • Antigens, CD / metabolism*
  • CD83 Antigen
  • Cell Differentiation
  • Disease Models, Animal
  • Epithelial Cells / metabolism*
  • Exosomes / metabolism*
  • Hypersensitivity / immunology*
  • Immune Tolerance
  • Immunoglobulins / metabolism*
  • Lymphocyte Activation
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Ovalbumin / immunology
  • Respiratory Hypersensitivity / immunology*
  • Respiratory Mucosa / immunology*
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Allergens
  • Antigens, CD
  • Immunoglobulins
  • Membrane Glycoproteins
  • Ovalbumin