Role of kinins in seasonal allergic rhinitis: Icatibant, a bradykinin B2 receptor antagonist, abolishes the hyperresponsiveness and nasal eosinophilia induced by antigen

• Published in: Journal of allergy and clinical immunology 2001-01, Vol.107 (1), p.105-113
• Main Authors: Turner, Paul, Dear, James, Scadding, Glenis, Foreman, John C.
• Format: Article
• Language: English
• Subjects: Adult; Aerosols - administration & dosage; Antigens - adverse effects; Biological and medical sciences; Bradykinin - administration & dosage; Bradykinin - analogs & derivatives; Bradykinin - therapeutic use; Bradykinin Receptor Antagonists; Bronchial Hyperreactivity - prevention & control; Cross-Over Studies; Eosinophilia - chemically induced; Eosinophilia - immunology; Histamine and antagonists. Allergy; Humans; Kinins - physiology; Medical sciences; Middle Aged; Nasal Cavity - cytology; Nasal Provocation Tests; Pharmacology. Drug treatments; Rhinitis - chemically induced; Rhinitis, Allergic, Seasonal - physiopathology; Time Factors
• ISSN: 0091-6749; 1097-6825
• DOI: 10.1067/mai.2001.111145

Background: Icatibant, a bradykinin B2 receptor antagonist, inhibits the reduction in nasal patency after challenge with house dust mite antigen in sensitive subjects and abolishes the nasal hyperresponsiveness induced by platelet-activating factor in nonatopic subjects. Objective: We sought to investigate the effect of icatibant on the response to nasal antigen challenge in subjects with seasonal allergic rhinitis. Methods: Patients allergic to grass pollen antigen (n = 9-13) were included in a double-blind, randomized-block, placebo-controlled, crossover study outside the pollen season. Subjects first received an intranasal spray of icatibant (200 μg per nostril) or a saline control. Subjects were then challenged with antigen or diluent (control), and their responses were monitored by using acoustic rhinometry. Six hours later, nasal lavage fluid was collected and quantified for inflammatory cells and various inflammatory mediators (kinin, eosinophil cationic protein, IL-5, and IL-8). At 24 hours, the response of the nasal airways to 200 μg of histamine was assessed, and a further nasal lavage was carried out. Results: Antigen challenge caused a significant increase in nasal obstruction and albumin extravasation, which was not affected by icatibant. Nasal hyperresponsiveness to histamine was present 24 hours after antigen and was abolished by pretreatment with icatibant. Icatibant also reduced the antigen-induced increase in eosinophils, eosinophil cationic protein, kinin, and IL-8 in nasal lavage fluid. Conclusion: Pretreatment with icatibant does not affect the acute inflammatory response in seasonal allergic rhinitis. However, our results imply the involvement of kinins and the bradykinin B2 receptor in the development of antigen-induced hyperresponsiveness and the associated eosinophilia in the human nasal airway. (J Allergy Clin Immunol 2001;107:105-13.)