Preservation of epithelial cell barrier function and muted inflammation in resistance to allergic rhinoconjunctivitis from house dust mite challenge

J Allergy Clin Immunol. 2017 Mar;139(3):844-854. doi: 10.1016/j.jaci.2016.08.019. Epub 2016 Sep 19.

Abstract

Background: An emerging paradigm holds that resistance to the development of allergic diseases, including allergic rhinoconjunctivitis, relates to an intact epithelial/epidermal barrier during early childhood. Conceivably, the immunologic and genomic footprint of this resistance is preserved in nonatopic, nonallergic adults and is unmasked during exposure to an aeroallergen.

Objective: The aim of this study was to obtain direct support of the epithelial/epidermal barrier model for allergic rhinoconjunctivitis.

Methods: Twenty-three adults allergic to house dust mites (HDMs) (M+) and 15 nonsensitive, nonallergic (M-) participants completed 3-hour exposures to aerosolized HDM (Dermatophagoides pteronyssinus) powder on 4 consecutive days in an allergen challenge chamber. We analyzed: (1) peripheral blood leukocyte levels and immune responses; and (2) RNA sequencing-derived expression profiles of nasal cells, before and after HDM exposure.

Results: On HDM challenge: (1) only M+ persons developed allergic rhinoconjunctivitis symptoms; and (2) peripheral blood leukocyte levels/responses and gene expression patterns in nasal cells were largely concordant between M+ and M- participants; gross differences in these parameters were not observed at baseline (pre-exposure). Two key differences were observed. First, peripheral blood CD4+ and CD8+ T-cell activation levels initially decreased in M- participants versus increased in M+ participants. Second, in M- compared with M+ participants, genes that promoted epidermal/epithelial barrier function (eg, filament-aggregating protein [filaggrin]) versus inflammation (eg, chemokines) and innate immunity (interferon) were upregulated versus muted, respectively.

Conclusion: An imprint of resistance to HDM challenge in nonatopic, nonallergic adults was muted T-cell activation in the peripheral blood and inflammatory response in the nasal compartment, coupled with upregulation of genes that promote epidermal/epithelial cell barrier function.

Keywords: Allergen challenge chamber; RNA sequencing; epithelial barrier; house dust mites; rhinoconjunctivitis.

MeSH terms

  • Administration, Inhalation
  • Adult
  • Allergens / immunology*
  • Animals
  • Antigens, Dermatophagoides / immunology*
  • Conjunctivitis, Allergic / genetics
  • Conjunctivitis, Allergic / immunology*
  • Disease Resistance
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism
  • Female
  • Filaggrin Proteins
  • Humans
  • Leukocyte Count
  • Male
  • Nasal Mucosa / immunology
  • Nasal Mucosa / metabolism
  • Pyroglyphidae / immunology*
  • Rhinitis, Allergic / genetics
  • Rhinitis, Allergic / immunology*
  • Transcriptome

Substances

  • Allergens
  • Antigens, Dermatophagoides
  • FLG protein, human
  • Filaggrin Proteins