Effect of intranasal fluticasone proprionate on the immediate and late allergic reaction and nasal hyperreactivity in patients with a house dust mite allergy

Clin Exp Allergy. 1995 Oct;25(10):966-73. doi: 10.1111/j.1365-2222.1995.tb00399.x.

Abstract

Background: Patients with perennial allergic rhinitis develop nasal symptoms not only after allergen exposure, but generally also after non-specific stimuli.

Objective: To evaluate the effect of 2 week's treatment with fluticasone propionate aqueous nasal spray (FPANS) on the nasal clinical response, inflammatory mediators and nasal hyperreactivity.

Methods: Twenty-four rhinitis patients allergic to house dust mite (HDM), participated in a double-blind, placebo-controlled crossover study. After 2 week's treatment with placebo or 200 micrograms FPANS twice daily, patients were challenged with HDM extract. Symptoms were recorded and nasal lavages were collected for up to 9.5 h after challenge. Nasal hyperreactivity was determined by histamine challenge 24 h later.

Results: Because of a carry-over effect for the immediate symptom score, for this variable only the data from the first treatment period were used. FPANS treatment resulted in a significant decrease of nasal symptoms with 70%, 69% and 63% after 100, 1000 and 10,000 Biological Units (BU)/mL of HDM extract respectively. Active treatment resulted in a 76% decrease of the late-phase symptoms. FPANS treatment significantly reduced albumin influx after HDM 1000 BU/mL with 62% and tended to reduce tryptase release after HDM 1000 BU/mL (P = 0.0629). During the late phase FPANS treatment reduced albumin influx with 67% and eosinophil cationic protein (ECP) release with 83%. No effect of FPANS was seen on histamine levels. FPANS significantly decreased histamine-induced symptom score with 34%, secretion with 32% and sneezes with 41%.

Conclusion: FPANS significantly inhibits the immediate and late allergic response, and nasal hyperreactivity, probably by suppressing mast cells and eosinophils in the nasal mucosa.

Publication types

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

MeSH terms

  • Administration, Intranasal
  • Adult
  • Androstadienes / administration & dosage
  • Androstadienes / therapeutic use*
  • Animals
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / therapeutic use
  • Antigens, Dermatophagoides
  • Cross-Over Studies
  • Double-Blind Method
  • Female
  • Fluticasone
  • Glycoproteins / immunology*
  • Humans
  • Hypersensitivity, Delayed / drug therapy*
  • Hypersensitivity, Delayed / immunology
  • Hypersensitivity, Immediate / drug therapy*
  • Hypersensitivity, Immediate / immunology
  • Male
  • Middle Aged
  • Mites / immunology*
  • Nasal Mucosa / drug effects*
  • Nasal Mucosa / immunology*
  • Nasal Mucosa / pathology
  • Rhinitis, Allergic, Perennial / drug therapy*
  • Rhinitis, Allergic, Perennial / immunology

Substances

  • Androstadienes
  • Anti-Inflammatory Agents
  • Antigens, Dermatophagoides
  • Glycoproteins
  • Fluticasone