The effect of Fel d 1-derived T-cell peptides on upper and lower airway outcome measurements in cat-allergic subjects

Allergy. 2005 Oct;60(10):1269-74. doi: 10.1111/j.1398-9995.2005.00885.x.

Abstract

Background: We previously showed that overlapping Fel d 1-derived T-cell peptides inhibited surrogate markers of allergy (i.e. early and late-phase skin reactions and T-cell function) in cat allergic subjects. The present pilot study was designed to determine whether this treatment affected clinically relevant outcome measurements such as the allergen-induced nasal and bronchial reactions, and asthma/rhinitis quality of life (QOL).

Methods: Sixteen cat-allergic asthmatic subjects who gave a dual (early and late) asthmatic response (DAR) to inhaled cat allergen were randomly assigned to receive either Fel d 1 peptides (approximately 300 mug in increasing, divided doses) or placebo (8 active : 8 placebo). Twelve single early responders (SER) were also studied in an open fashion design. Allergen-induced bronchial and nasal measurements as well as the QOL was measured at baseline, 4-8 weeks (follow-up 1 (FU1)) and 3-4 months (FU2).

Results: In the active, but not placebo, group there were significant decreases in the late asthmatic reaction (LAR) to whole cat dander (P = 0.03) at FU2 but with no between group difference. There were also significant improvements in asthma quality of life (QOL) scores [asthma-activity limitation (P = 0.014); rhinitis-sleep (P = 0.024), non-nose/non-eye symptoms (P = 0.031), nasal problems (P = 0.015)]. In the open study Fel d 1 peptide treatment resulted in significant decreases in number of sneezes (P = 0.05), weight of nasal secretions (P = 0.04) and nasal blockage (P = 0.01) following allergen challenge.

Conclusions: Multiple, short, overlapping Fel d 1 T-cell peptides have potential for inhibiting upper and lower airway outcome measurements in cat allergic patients. Larger, dose-ranging, studies are required before firm conclusions on clinical efficacy of peptide allergen therapy can be made.

Publication types

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

MeSH terms

  • Adult
  • Animals
  • Asthma / therapy*
  • Cats / immunology*
  • Desensitization, Immunologic*
  • Female
  • Glycoproteins / chemistry
  • Glycoproteins / therapeutic use*
  • Humans
  • Hypersensitivity / etiology
  • Hypersensitivity / therapy*
  • Immune Tolerance
  • Male
  • Middle Aged
  • Peptides / chemical synthesis
  • Peptides / chemistry
  • Peptides / therapeutic use*
  • Rhinitis / therapy*
  • T-Lymphocytes / immunology
  • Treatment Outcome

Substances

  • Glycoproteins
  • Peptides
  • Fel d 1 protein, Felis domesticus