The macrophage mannose receptor induces IL-17 in response to Candida albicans

Cell Host Microbe. 2009 Apr 23;5(4):329-40. doi: 10.1016/j.chom.2009.02.006.

Abstract

The cytokine IL-17 controls neutrophil-mediated inflammatory responses. The pattern recognition receptor(s) that induce Th17 responses during infection, in the absence of artificial mitogenic stimulation with anti-CD3/anti-CD28 antibodies, remain obscure. We investigated the innate immune receptors and pathogen-associated molecular patterns involved in triggering Th17 responses during pathogen-specific host defense. The prototypic fungal pathogen Candida albicans was found to induce IL-17 more potently than Gram-negative bacteria. Candida mannan, but not zymosan, beta-glucans, Toll-like receptor (TLR) agonists, or the NOD2 ligand MDP, induced IL-17 production in the absence of anti-CD3/anti-CD28 antibodies. Candida-induced IL-17 response was dependent on antigen-presenting cells and the macrophage mannose receptor (MR), demonstrating that Candida mannan is not simply a mitogenic stimulus. The TLR2/dectin-1 pathway, but not TLR4 or NOD2, amplified MR-induced IL-17 production. This study identifies the specific pattern recognition receptors that trigger the Th17 response induced by a human pathogen in the absence of mitogenic stimulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Candida albicans / immunology*
  • Cell Wall / immunology*
  • Cells, Cultured
  • Humans
  • Interleukin-17 / biosynthesis*
  • Lectins, C-Type / immunology*
  • Macrophages / immunology*
  • Mannans / immunology*
  • Mannose Receptor
  • Mannose-Binding Lectins / immunology*
  • Membrane Proteins / immunology
  • Nerve Tissue Proteins / immunology
  • Receptors, Cell Surface / immunology*
  • Toll-Like Receptor 2 / immunology

Substances

  • Interleukin-17
  • Lectins, C-Type
  • Mannans
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Receptors, Cell Surface
  • TLR2 protein, human
  • Toll-Like Receptor 2
  • dectin 1