Nasal eosinophilia and IL-5 mRNA expression in seasonal allergic rhinitis induced by natural allergen exposure: effect of topical corticosteroids

J Allergy Clin Immunol. 1998 Oct;102(4 Pt 1):610-7. doi: 10.1016/s0091-6749(98)70277-5.

Abstract

Background: Nasal allergen provocation in patients with allergic rhinitis leads to expression of the proeosinophilic cytokines IL-5 and GM-CSF and tissue eosinophilia.

Objective: We sought to examine the effect of natural seasonal allergen exposure on IL-5 and GM-CSF mRNA expression and nasal eosinophilia and to evaluate the effects of topical corticosteroid therapy on these responses.

Methods: Nasal biopsy specimens were collected from 46 grass pollen-sensitive patients with seasonal rhinitis before the grass pollen season. A second biopsy specimen was collected during the pollen season, by which time patients had received 6 weeks treatment with either fluticasone propionate (200 micro(g) twice daily) or placebo nasal spray.

Results: Fluticasone treatment was clinically effective (P <.005). Patients receiving placebo, but not fluticasone, showed increased numbers of epithelial and submucosal EG2+ eosinophils (P <.005) and IL-5 and GM-CSF mRNA-expressing cells (P <.0001) during the pollen season. Colocalization experiments showed that greater than 80% of IL-5 mRNA-expressing cells were submucosal CD3+ T cells in both groups. The numbers of submucosal CD3+ T cells did not increase during the pollen season or decrease with fluticasone treatment. Fluticasone also inhibited IL-5 secretion by grass pollen-stimulated peripheral blood T cells from patients with seasonal rhinitis (n = 5, inhibitory concentration of 50% = 10(-9) to 10(-10) mol/L).

Conclusions: These results suggest that topical corticosteroids may reduce eosinophilia in seasonal rhinitis by inhibiting T cell IL-5 production.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Androstadienes / administration & dosage
  • Androstadienes / therapeutic use*
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / therapeutic use*
  • Biopsy
  • CD3 Complex / analysis
  • Cells, Cultured
  • Eosinophilia / complications
  • Eosinophilia / metabolism*
  • Eosinophilia / pathology
  • Fluticasone
  • Glucocorticoids
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics
  • Humans
  • In Situ Hybridization
  • Interleukin-5 / biosynthesis*
  • Interleukin-5 / genetics
  • Nasal Mucosa / drug effects
  • Nasal Mucosa / metabolism*
  • Nasal Mucosa / pathology
  • Poaceae
  • Pollen
  • RNA, Messenger / metabolism*
  • Rhinitis, Allergic, Seasonal / complications
  • Rhinitis, Allergic, Seasonal / metabolism*
  • Rhinitis, Allergic, Seasonal / pathology
  • Skin Tests
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / immunology

Substances

  • Androstadienes
  • Anti-Inflammatory Agents
  • CD3 Complex
  • Glucocorticoids
  • Interleukin-5
  • RNA, Messenger
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Fluticasone