Epithelial control of the human pDC response to extracellular bacteria

Eur J Immunol. 2013 May;43(5):1264-73. doi: 10.1002/eji.201242990. Epub 2013 Mar 6.

Abstract

Plasmacytoid pre-dendritic cells (pDCs) are specialized in responding to nucleic acids, and link innate with adaptive immunity. Although the response of pDCs to viruses is well established, whether pDCs can respond to extracellular bacteria remains controversial. Here, we demonstrate that extracellular bacteria such as Neisseria meningitidis, Haemophilus influenzae, and Staphylococcus aureus activate pDCs to produce IFN-α, TNF-α, IL-6, and to upregulate CD86 expression. We observed that pDCs were present within tonsillar crypts and oro-nasopharyngeal epithelium, where they may contact extracellular bacteria, in situ. Tonsil epithelium-conditioned supernatants inhibited IFN-α, TNF-α, and IL-6 triggered by the direct contact of N. meningitidis or S. aureus with pDCs. However, pDC priming of naive T cells was not affected, suggesting that tonsil epithelium micro-environment limits local inflammation while preserving adaptive immunity in response to extracellular bacteria. Our results reveal an important and novel function of pDCs in the initiation of the mucosal innate and adaptive immunity to extracellular bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity
  • Adenoids / cytology*
  • Adenoids / immunology
  • Adenoids / microbiology
  • B7-2 Antigen / genetics
  • B7-2 Antigen / immunology
  • Cell Communication
  • Coculture Techniques
  • Culture Media, Conditioned / pharmacology
  • Dendritic Cells / cytology*
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Dendritic Cells / microbiology
  • Epithelial Cells / cytology*
  • Epithelial Cells / immunology
  • Epithelial Cells / microbiology
  • Haemophilus influenzae / growth & development
  • Humans
  • Immunity, Innate
  • Immunity, Mucosal*
  • Interferon-alpha / biosynthesis
  • Interferon-alpha / immunology
  • Interleukin-6 / biosynthesis
  • Interleukin-6 / immunology
  • Lymphocyte Activation
  • Neisseria meningitidis / growth & development
  • Respiratory Mucosa / cytology*
  • Respiratory Mucosa / immunology
  • Respiratory Mucosa / microbiology
  • Staphylococcus aureus / growth & development
  • T-Lymphocytes / cytology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology
  • Up-Regulation

Substances

  • B7-2 Antigen
  • CD86 protein, human
  • Culture Media, Conditioned
  • Interferon-alpha
  • Interleukin-6
  • Tumor Necrosis Factor-alpha