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扎鲁司特(安可来)对炎症细胞介质的影响:节段性抗原激发后的支气管肺泡灌洗结果

Effect of zafirlukast (Accolate) on cellular mediators of inflammation: bronchoalveolar lavage fluid findings after segmental antigen challenge.

作者信息

Calhoun W J, Lavins B J, Minkwitz M C, Evans R, Gleich G J, Cohn J

机构信息

Division of Pulmonary, Allergy, and Critical Care Medicine, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261, USA.

出版信息

Am J Respir Crit Care Med. 1998 May;157(5 Pt 1):1381-9. doi: 10.1164/ajrccm.157.5.9609014.

Abstract

The effect of zafirlukast (Z) to alter the inflammatory response to segmental antigen challenge (SAC) was assessed by bronchoalveolar lavage (BAL) in this double-blind, placebo-controlled, two-period, crossover trial in 11 allergic asthmatic patients. Patients with asthma and positive skin tests to antigen received 7 d of treatment with Z (20 mg twice daily) or placebo (P) during two trial periods 14 to 21 d apart. At steady state (Day 5), patients underwent SAC followed by BAL immediately after challenge and 48 h later. Purified alveolar macrophages were analyzed ex vivo for phorbol myristate acetate (PMA)-driven superoxide release. Results were analyzed by analysis of variance (ANOVA). Forty-eight hours after SAC, Z therapy was associated with significantly reduced BAL lymphocytes and alcian blue-positive cells (presumably basophils) compared with P (p < 0.01), with a trend toward reduced numbers of alveolar macrophages (p = 0.06). PMA-driven superoxide release by purified alveolar macrophages was significantly reduced 48 h after SAC in the Z versus P arms (p < 0.05). Reduction of basophil influx, mediator release, and cellular activation may be important in attenuating the late phase of asthma. Collectively, the data suggest that zafirlukast therapy alters cellular infiltration and activation associated with antigen challenge.

摘要

在这项针对11名过敏性哮喘患者的双盲、安慰剂对照、两阶段交叉试验中,通过支气管肺泡灌洗(BAL)评估了扎鲁司特(Z)改变对节段性抗原激发(SAC)的炎症反应的效果。哮喘患者且皮肤抗原试验呈阳性者在两个相隔14至21天的试验阶段接受7天的Z治疗(20毫克,每日两次)或安慰剂(P)治疗。在稳态时(第5天),患者接受SAC,激发后立即及48小时后进行BAL。对纯化的肺泡巨噬细胞进行体外分析,检测佛波酯肉豆蔻酸酯(PMA)驱动的超氧化物释放。结果采用方差分析(ANOVA)进行分析。SAC后48小时,与P相比,Z治疗组的BAL淋巴细胞和阿尔新蓝阳性细胞(可能是嗜碱性粒细胞)显著减少(p < 0.01),肺泡巨噬细胞数量有减少趋势(p = 0.06)。在Z组与P组中,SAC后48小时纯化肺泡巨噬细胞经PMA驱动的超氧化物释放显著减少(p < 0.05)。嗜碱性粒细胞流入、介质释放和细胞活化的减少可能在减轻哮喘晚期症状方面具有重要作用。总体而言,数据表明扎鲁司特治疗可改变与抗原激发相关的细胞浸润和活化。

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