Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo

J Exp Med. 2014 Jul 28;211(8):1657-72. doi: 10.1084/jem.20131800.

Abstract

Eosinophils natively inhabit the small intestine, but a functional role for them there has remained elusive. Here, we show that eosinophil-deficient mice were protected from induction of Th2-mediated peanut food allergy and anaphylaxis, and Th2 priming was restored by reconstitution with il4(+/+) or il4(-/-) eosinophils. Eosinophils controlled CD103(+) dendritic cell (DC) activation and migration from the intestine to draining lymph nodes, events necessary for Th2 priming. Eosinophil activation in vitro and in vivo led to degranulation of eosinophil peroxidase, a granule protein whose enzymatic activity promoted DC activation in mice and humans in vitro, and intestinal and extraintestinal mouse DC activation and mobilization to lymph nodes in vivo. Further, eosinophil peroxidase enhanced responses to ovalbumin seen after immunization. Thus, eosinophils can be critical contributors to the intestinal immune system, and granule-mediated shaping of DC responses can promote both intestinal and extraintestinal adaptive immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity / drug effects
  • Adaptive Immunity / immunology*
  • Animals
  • Antigen-Presenting Cells / drug effects
  • Antigen-Presenting Cells / immunology
  • Antigens, CD / metabolism
  • CD11c Antigen / metabolism
  • Cell Degranulation / drug effects
  • Cell Movement / drug effects
  • Cross-Priming / drug effects
  • Cross-Priming / immunology
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Eosinophils / immunology*
  • Eosinophils / ultrastructure
  • Erythropoietin / pharmacology
  • Gastrointestinal Tract / cytology*
  • Humans
  • Immunization
  • Integrin alpha Chains / metabolism
  • Interleukin-4 / biosynthesis
  • Mice
  • Th2 Cells / drug effects
  • Th2 Cells / immunology*

Substances

  • Antigens, CD
  • CD11c Antigen
  • Integrin alpha Chains
  • alpha E integrins
  • Erythropoietin
  • Interleukin-4