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急性哮喘中变应原暴露会导致血小板活化因子(PAF)的释放,这已通过血小板对PAF脱敏得到证实。

Allergen exposure in acute asthma causes the release of platelet-activating factor (PAF) as demonstrated by the desensitization of platelets to PAF.

作者信息

Beer J H, Wüthrich B, von Felten A

机构信息

Department of Medicine, University Hospital, Bern, Switzerland.

出版信息

Int Arch Allergy Immunol. 1995 Mar;106(3):291-6. doi: 10.1159/000236857.

Abstract

Platelet-activating factor (PAF) is released in IgE-mediated allergic diseases. The normal level, the method of its determination and its clinical importance are subject of controversy. We hypothesized that a functional assay could help to better analyze the actual concentrations in vivo because PAF may be released locally and is short-lived. An assay to detect PAF by the desensitized state of human platelets exposed to PAF in vitro or ex vivo was developed: We analyzed the synergistic platelet response to dual agonist stimulation at extraordinarily low doses (collagen 0.10 microgram/ml and PAF 2.5 x 10(-8) M) in aggregation and release reaction and its absence after previous exposure to PAF at concentrations between 5 x 10(-9) and 5 x 10(-11) M in vitro. The same test was then applied to examine the platelets from patients with IgE-mediated allergic asthma before and after inhalation of the specific allergen (inhalative provocation test; a reduction of the FEV1 by > 15% was considered positive). The lack of a synergistic response to collagen with PAF was found after preincubation of the platelets with 5 x 10(-9) M PAF and a reduction of +/- 50% with 5 x 10(-10) M in vitro. A significant reduction of the aggregation response (-56 +/- 18%) and of the release of beta-thromboglobulin (-75 +/- 24%) was found in 6 patients with a positive inhalative provocation test but not in 3 patients with a negative response.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

血小板活化因子(PAF)在IgE介导的过敏性疾病中释放。其正常水平、测定方法及其临床重要性存在争议。我们推测功能测定有助于更好地分析体内的实际浓度,因为PAF可能在局部释放且寿命短暂。我们开发了一种通过体外或离体暴露于PAF的人血小板脱敏状态来检测PAF的测定方法:我们分析了在极低剂量(胶原蛋白0.10微克/毫升和PAF 2.5×10⁻⁸M)下双重激动剂刺激时血小板在聚集和释放反应中的协同反应,以及在体外预先暴露于浓度介于5×10⁻⁹和5×10⁻¹¹M的PAF后该协同反应的缺失。然后将相同的测试应用于检查IgE介导的过敏性哮喘患者在吸入特定过敏原前后的血小板(吸入激发试验;FEV₁降低>15%被视为阳性)。在体外将血小板与5×10⁻⁹M PAF预孵育后,发现对胶原蛋白与PAF缺乏协同反应,而与5×10⁻¹⁰M预孵育后协同反应降低±50%。在6例吸入激发试验阳性的患者中发现聚集反应显著降低(-56±18%)和β-血小板球蛋白释放显著降低(-75±24%),但在3例阴性反应患者中未发现。(摘要截短于250字)

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