Cutting edge: Peyer's patch plasmacytoid dendritic cells (pDCs) produce low levels of type I interferons: possible role for IL-10, TGFbeta, and prostaglandin E2 in conditioning a unique mucosal pDC phenotype

J Immunol. 2007 Sep 1;179(5):2690-4. doi: 10.4049/jimmunol.179.5.2690.

Abstract

The organized lymphoid tissues of the intestine likely play an important role in the balance between tolerance harmless mucosal Ags and commensal bacteria and immunity to mucosal pathogens. We examined the phenotype and function of plasmacytoid dendritic cells (pDCs) from murine Peyer's patches (PPs). When stimulated with CpG-enriched oligodeoxynucleotides in vitro, PPs and spleen pDCs made equivalent levels of IL-12, yet PP pDCs were incapable of producing significant levels of type I IFNs. Three regulatory factors associated with mucosal tissues, PGE(2), IL-10, and TGFbeta, inhibited the ability of spleen pDCs to produce type I IFN in a dose-dependent fashion. These studies suggest that mucosal factors may regulate the production of type I IFN as well as IL-12 by pDCs. In the intestine, this may be beneficial in preventing harmful innate and adaptive immune responses to commensal microorganisms.

Publication types

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

MeSH terms

  • Animals
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Dinoprostone / pharmacology
  • Dinoprostone / physiology
  • Interferon Type I / biosynthesis*
  • Interferon Type I / genetics
  • Interleukin-10 / pharmacology
  • Interleukin-10 / physiology
  • Interleukin-12 / metabolism
  • Intestinal Mucosa / immunology*
  • Mice
  • Mice, Mutant Strains
  • Peyer's Patches / immunology*
  • RNA, Messenger / antagonists & inhibitors
  • RNA, Messenger / metabolism
  • Receptor, Interferon alpha-beta / genetics
  • Spleen / immunology
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta / physiology

Substances

  • Interferon Type I
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Interleukin-10
  • Receptor, Interferon alpha-beta
  • Interleukin-12
  • Dinoprostone