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早期迟发性过敏性皮肤炎症反应期间的细胞炎症反应和介质释放:西替利嗪的作用

Cellular inflammatory responses and mediator release during early developing late-phase allergic cutaneous inflammatory responses: effects of cetirizine.

作者信息

Atkins P C, Zweiman B, Moskovitz A, von Allmen C, Ciliberti M

机构信息

Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104-6057, USA.

出版信息

J Allergy Clin Immunol. 1997 Jun;99(6 Pt 1):806-11. doi: 10.1016/s0091-6749(97)80015-2.

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 specimens.

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.

摘要

背景

皮肤迟发性过敏反应的发展过程可通过皮肤腔室和活检方法相结合来进行表征。在先前的一些研究中,据报道西替利嗪可抑制迟发性反应中的介质释放和/或炎症细胞反应。

目的

本研究旨在通过使用皮肤腔室和皮肤活检标本确定西替利嗪对早期迟发性反应的影响。

方法

在15名敏感受试者中,在随机交叉治疗期间,用西替利嗪(20毫克/天)或安慰剂治疗7天,测量体液和细胞成分,评估花粉抗原6小时激发期间的皮肤腔室反应。获取下层真皮的活检标本。

结果

在西替利嗪治疗期间,对花粉抗原(34%,46%)、可待因(41%,65%)和组胺(38%,68%)的即刻风团和潮红反应受到显著(p < 0.01)抑制。然而,6小时时的明显迟发性反应未受影响。在西替利嗪和安慰剂治疗期间均观察到,在以下方面抗原部位有明显更多的积聚:(1)皮肤腔室中组胺、总细胞、乳铁蛋白和嗜酸性粒细胞阳离子蛋白的水平;(2)附加盖玻片上的嗜酸性粒细胞(总数和活化的);(3)下层真皮中乳铁蛋白和嗜酸性粒细胞阳离子蛋白的沉积。然而,与安慰剂治疗期相比,西替利嗪治疗期间这些反应无显著差异。

结论

西替利嗪治疗对早期迟发性反应中炎症细胞积聚并释放颗粒蛋白的持续模式无影响。

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