Clec4A4 is a regulatory receptor for dendritic cells that impairs inflammation and T-cell immunity

Nat Commun. 2016 Apr 12:7:11273. doi: 10.1038/ncomms11273.

Abstract

Dendritic cells (DCs) comprise several subsets that are critically involved in the initiation and regulation of immunity. Clec4A4/DC immunoreceptor 2 (DCIR2) is a C-type lectin receptor (CLR) exclusively expressed on CD8α(-) conventional DCs (cDCs). However, how Clec4A4 controls immune responses through regulation of the function of CD8α(-) cDCs remains unclear. Here we show that Clec4A4 is a regulatory receptor for the activation of CD8α(-) cDCs that impairs inflammation and T-cell immunity. Clec4a4(-/-)CD8α(-) cDCs show enhanced cytokine production and T-cell priming following Toll-like receptor (TLR)-mediated activation. Furthermore, Clec4a4(-/-) mice exhibit TLR-mediated hyperinflammation. On antigenic immunization, Clec4a4(-/-) mice show not only augmented T-cell responses but also progressive autoimmune pathogenesis. Conversely, Clec4a4(-/-) mice exhibit resistance to microbial infection, accompanied by enhanced T-cell responses against microbes. Thus, our findings highlight roles of Clec4A4 in regulation of the function of CD8α(-) cDCs for control of the magnitude and quality of immune response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Infections / immunology
  • Bacterial Infections / prevention & control
  • CD4-Positive T-Lymphocytes / immunology
  • CD8 Antigens / metabolism
  • CD8-Positive T-Lymphocytes / immunology
  • Cytokines / biosynthesis
  • Dendritic Cells / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Epitopes / immunology
  • Host-Pathogen Interactions / immunology
  • Immunity, Cellular*
  • Inflammation / pathology*
  • Ligands
  • Mice, Inbred C57BL
  • Polysaccharides / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / metabolism*
  • Receptors, Immunologic / chemistry
  • Receptors, Immunologic / metabolism*
  • Retroviridae / metabolism
  • T-Lymphocytes / immunology*
  • Toll-Like Receptors / metabolism
  • Transduction, Genetic

Substances

  • CD8 Antigens
  • Cytokines
  • DCIR2 protein, mouse
  • Epitopes
  • Ligands
  • Polysaccharides
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Toll-Like Receptors