Effect of intranasal fluticasone propionate on the immediate and late allergic reaction and nasal hyperreactivity in patients with a house dust mite allergy

Effect of intranasal fluticasone propionate on the immediate and late allergic reaction and nasal hyperreactivity in patients with a house dust mite allergy
复制标题

DOI:
10.1111/j.1365-2222.1995.tb00399.x
复制
发表时间:
1995-01-01
影响因子:
6.1
通讯作者:
Gerth Van Wijk, R.
Gerth Van Wijk, R.
中科院分区:
医学2区
文献类型:
--
作者:
De Graaf-In't Veld, C.;Garrelds, I. M.;Gerth Van Wijk, R.

文献摘要

被引文献

相似文献

背景资料:常年性变应性鼻炎患者不仅在接触过敏原后出现鼻部症状,而且通常在非特异性刺激后也会出现鼻部症状。目的:评价丙酸氟替卡松鼻喷雾剂(FPANS)治疗2周对鼻腔临床反应、炎症介质和鼻高反应性的影响。方法:24例屋尘螨过敏性鼻炎患者参加了一项双盲、安慰剂对照的交叉研究。用安慰剂或200 μ g FPANS每日两次治疗2周后,用HDM提取物激发患者。记录症状,并在攻毒后收集鼻灌洗液长达9.5 h。24 h后通过组胺激发测定鼻高反应性。结果:由于即时症状评分的结转效应,该变量仅使用第一个治疗期的数据。FPANS治疗导致鼻部症状显著减少,在100、1000和10000生物单位(BU)/mL HDM提取物后分别减少70%、69%和63%。积极治疗导致晚期症状减少76%。FPANS治疗显著减少HDM 1000 BU/mL后的白蛋白内流62%,并倾向于减少HDM 1000 BU/mL后的类胰蛋白酶释放(P=0.0629)。在晚期阶段,FPANS治疗使白蛋白内流减少67%,嗜酸性粒细胞阳离子蛋白(ECP)释放减少83%。FPANS对组胺水平无影响。FPANS显著降低了组胺诱导的症状评分(34%)、分泌物(32%)和打喷嚏(41%)。结论FPANS可显著抑制鼻粘膜的即刻和迟发性变态反应及鼻高反应性,其机制可能与抑制鼻粘膜肥大细胞和嗜酸性粒细胞有关。
Background: Patients with perennial allergic rhinitis develop nasal symptoms not only after allergen exposure, but generally also after non-specific stimuli. Objective: To evaluate the effect of 2 week's treatment with fluticasone propionate aqueous nasal spray (FPANS) on the nasal clinical response, inflammatory mediators and nasal hyperreactivity. Methods: Twenty-four rhinitis patients allergic to house dust mite (HDM), participated in a double-blind, placebo-controlled crossover study. After 2 week's treatment with placebo or 200 mu-g FPANS twice daily, patients were challenged with HDM extract. Symptoms were recorded and nasal lavages were collected for up to 9.5 h after challenge. Nasal hyperreactivity was determined by histamine challenge 24 h later. Results: Because of a carry-over effect for the immediate symptom score, for this variable only the data from the first treatment period were used. FPANS treatment resulted in a significant decrease of nasal symptoms with 70%, 69% and 63% after 100, 1000 and 10000 Biological Units (BU)/mL of HDM extract respectively. Active treatment resulted in a 76% decrease of the late-phase symptoms. FPANS treatment significantly reduced albumin influx after HDM 1000 BU/mL with 62% and tended to reduce tryptase release after HDM 1000 BU/mL (P=0.0629). During the late phase FPANS treatment reduced albumin influx with 67% and eosinophil cationic protein (ECP) release with 83%. No effect of FPANS was seen on histamine levels. FPANS significantly decreased histamine-induced symptom score with 34%, secretion with 32% and sneezes with 41 %. Conclusion FPANS significantly inhibits the immediate and late allergic response, and nasal hyperreactivity, probably by suppressing mast cells and eosinophils in the nasal mucosa.