Evaluation of cytokines in nasal secretions after nasal antigen challenge: lack of influence of antihistamines

Ann Allergy Asthma Immunol. 2002 May;88(5):457-62. doi: 10.1016/S1081-1206(10)62382-4.

Abstract

Background: Previous studies of inflammation in allergic rhinitis using nasal irrication have been unsatisfactory because of 1) poor reproducibility; 2) the tendency of irrigation to overdilute mediators; and 3) the failure of this technique to evaluate interstitial concentrations of relevant mediators. For this study we used filter paper as a matrix to collect nasal secretions in patients undergoing nasal antigen challenge.

Objective: To evaluate inflammatory mediators of allergen-induced rhinitis during a clinical trial of fexofenadine.

Methods: Subjects evaluated at a referral medical center were placed on traditional dosing of fexofenadine at 60 mg, twice daily, or placebo in a double-blind, crossover fashion for 1 week before the nasal challenge. Nasal challenge was performed with nasal insufflation of either 1,000 AU timothy or 0.1 mL ragweed (1:100 wt/vol) extract outside the pollen season. Nasal secretions were collected at baseline and then at 2, 4, and 6 hours after nasal challenge. Secretions were evaluated for expression of the cellular adhesion molecule-1, tumor necrosis factor (TNF)-alpha, interleukin (IL)-4, IL-10, macrophage inflammatory protein (MIP)-1alpha, and granulocyte-macrophage colony-stimulating factor (GM-CSF) using commercially available enzyme-linked immunoadsorbent assay kits. Patients' symptom scores were evaluated during the nasal challenge.

Results: Significantly (P < 0.05) increased peak levels of TNF-alpha, IL-4, IL-10, and MIP-1alpha were detected after antigen challenge as compared with baseline levels. There was a nonsignificant trend toward an increase in GM-CSF after antigen challenge (P = 0.07). There was no difference in the peak levels of TNF-alpha, IL-4, IL-10, MIP-1alpha, or GM-CSF measured when patients were on fexofenadine versus placebo. Finally, there were no significant differences in patients' symptom scores during antigen challenge when subjects were on fexofenadine versus placebo.

Conclusions: Collection of nasal secretions using a filter paper matrix provides a reproducible model for accurately detecting and evaluating changes in cytokine levels after nasal challenge. Cytokine levels tend to peak 3 to 4 hours after antigen challenge. Standard doses of fexofenadine do not seem to have a mitigating effect on the production of these cytokines. Symptoms of allergic rhinitis using this type of antigen challenge did not differ from treatment with fexofenadine versus placebo.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anti-Allergic Agents / therapeutic use*
  • Chemokine CCL3
  • Chemokine CCL4
  • Cross-Over Studies
  • Cytokines / analysis*
  • Double-Blind Method
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor / analysis
  • Histamine H1 Antagonists / therapeutic use*
  • Humans
  • Intercellular Adhesion Molecule-1 / analysis
  • Interleukin-4 / analysis
  • Macrophage Inflammatory Proteins / analysis
  • Middle Aged
  • Nasal Mucosa / immunology
  • Nasal Mucosa / metabolism*
  • Nasal Provocation Tests*
  • Plant Proteins / administration & dosage
  • Plant Proteins / adverse effects
  • Rhinitis, Allergic, Perennial / chemically induced
  • Rhinitis, Allergic, Perennial / drug therapy*
  • Rhinitis, Allergic, Perennial / immunology
  • Terfenadine / analogs & derivatives*
  • Terfenadine / therapeutic use*
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Anti-Allergic Agents
  • Chemokine CCL3
  • Chemokine CCL4
  • Cytokines
  • Histamine H1 Antagonists
  • Macrophage Inflammatory Proteins
  • Plant Proteins
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1
  • Interleukin-4
  • Terfenadine
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • fexofenadine