Prolonged ovalbumin challenge facilitates Th17 polarization in sensitized mice

Inflamm Res. 2010 Jul;59(7):561-9. doi: 10.1007/s00011-010-0162-z. Epub 2010 Feb 14.

Abstract

Objective and design: In this study, we explored whether prolonged ovalbumin (OVA) exposure in sensitized mice created an environment suitable for Th17 differentiation.

Materials and methods: BALB/c and C57BL/6 mice (n = 36), after intraperitoneal OVA sensitization on days 0 and 12, received prolonged OVA aerosol challenges up to day 55. Airway inflammatory cell levels, cytokine profiles, and Th17 cell infiltration were evaluated after sacrifice.

Results: Prolonged OVA challenge caused inflammation that was characterized by raised influxes of airway macrophages and neutrophils. Following long-term exposure, Th17 cytokines and Th17 cell numbers progressively increased in the lung (P < 0.05) along with increased production of Th17 polarization-related factors, including TGF-beta, IL-6, and IL-23. The lineage-specific transcription factor for Th17 subsets, RORgammat, displayed similar upregulation throughout the OVA challenge (P < 0.05).

Conclusions: Prolonged OVA challenge induces an environment that facilitates Th17 polarization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bronchial Hyperreactivity / immunology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Differentiation
  • Cell Polarity*
  • Cytokines / immunology*
  • Interleukin-23 / immunology
  • Interleukin-6 / immunology
  • Lung / cytology
  • Lung / drug effects
  • Lung / immunology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / immunology
  • Ovalbumin / immunology
  • Ovalbumin / pharmacology*
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / immunology*
  • Transforming Growth Factor beta / immunology

Substances

  • Cytokines
  • Interleukin-23
  • Interleukin-6
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Transforming Growth Factor beta
  • Ovalbumin