Selective blockade of the inhibitory Fcgamma receptor (FcgammaRIIB) in human dendritic cells and monocytes induces a type I interferon response program

J Exp Med. 2007 Jun 11;204(6):1359-69. doi: 10.1084/jem.20062545. Epub 2007 May 14.

Abstract

The ability of dendritic cells (DCs) to activate immunity is linked to their maturation status. In prior studies, we have shown that selective antibody-mediated blockade of inhibitory FcgammaRIIB receptor on human DCs in the presence of activating immunoglobulin (Ig) ligands leads to DC maturation and enhanced immunity to antibody-coated tumor cells. We show that Fcgamma receptor (FcgammaR)-mediated activation of human monocytes and monocyte-derived DCs is associated with a distinct gene expression pattern, including several inflammation-associated chemokines, as well as type 1 interferon (IFN) response genes, including the activation of signal transducer and activator of transcription 1 (STAT1). FcgammaR-mediated STAT1 activation is rapid and requires activating FcgammaRs. However, this IFN response is observed without a detectable increase in the expression of type I IFNs themselves or the need to add exogenous IFNs. Induction of IFN response genes plays an important role in FcgammaR-mediated effects on DCs, as suppression of STAT1 by RNA interference inhibited FcgammaR-mediated DC maturation. These data suggest that the balance of activating/inhibitory FcgammaRs may regulate IFN signaling in myeloid cells. Manipulation of FcgammaR balance on DCs and monocytes may provide a novel approach to regulating IFN-mediated pathways in autoimmunity and human cancer.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / pharmacology
  • Blotting, Western
  • Cytokines / metabolism
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Flow Cytometry
  • Gene Expression Profiling
  • Gene Expression Regulation / immunology*
  • Humans
  • Interferon Type I / immunology*
  • Interferon Type I / metabolism
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Oligonucleotide Array Sequence Analysis
  • RNA Interference
  • Receptors, IgG / antagonists & inhibitors*
  • STAT1 Transcription Factor / genetics
  • Signal Transduction / immunology*

Substances

  • Antibodies
  • Cytokines
  • FCGR2B protein, human
  • Interferon Type I
  • Receptors, IgG
  • STAT1 Transcription Factor
  • STAT1 protein, human