Cellular inflammatory responses and mediator release during early developing late-phase allergic cutaneous inflammatory responses: Effects of cetirizine - 09/09/11
Abstract |
Background: Events in developing cutaneous late-phase allergic reactions can be characterized by a combination of skin chamber and biopsy approaches. In some previous studies, cetirizine reportedly inhibited mediator release and/or inflammatory cell responses in late-phase reactions.
Objective: This study was carried out to determine the effects of cetirizine on early late-phase reactions by using skin chamber and skin biopsy speciments.
Methods: Skin chamber responses during a 6-hour challenge with pollen antigens were assessed in 15 sensitive subjects during randomized, crossover treatment with cetirizine (20 mg/day) or placebo for 7-day periods with measurements of humoral and cellular components. Biopsy specimens of the underlying dermis were obtained.
Results: During cetirizine treatment, there was significant (p<0.01) inhibition of immediate wheal and flare reactions to pollen antigens (34, 46%), codeine (41, 65%), and histamine (38, 68%). However, gross late-phase reactions at 6 hours were unaffected. During both cetirizine and placebo treatment, there was significantly greater accumulation at antigen sites in: (1) skin chamber levels of histamine, total cells, lactoferrin, and eosinophil cationic protein; (2) eosinophils (total and activated) on appended cover glasses; (3) deposition of lactoferrin and eosinophil cationic protein in the underlying dermis. However, these responses were not significantly different during cetirizine treatment compared with placebo treatment periods.
Conclusion: A persistent pattern of inflammatory cell accumulation with release of granule proteins during early late-phase reactions was unaffected by cetirizine treatment.
Le texte complet de cet article est disponible en PDF.Key words : Late-phase response, cutaneous allergic response, neutrophils, eosinophils, lactoferrin, ECP, cetirizine
| 1 | Supported by National Institutes of Health grant RO1 AI 14332 and Pfizer Pharmaceuticals |
Vol 99 - N° 6P1
P. 806-811 - juin 1997 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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