首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Effect of topical fluticasone propionate on the mucosal allergic response induced by ragweed allergen and diesel exhaust particle challenge.
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Effect of topical fluticasone propionate on the mucosal allergic response induced by ragweed allergen and diesel exhaust particle challenge.

机译:局部使用丙酸氟替卡松对豚草过敏原和柴油机尾气颗粒激发所致的粘膜过敏反应的影响。

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Glucocorticoids block the local allergic response in a variety of ways. However, studies have also shown that glucocorticoids increase in vitro IgE synthesis and that treatment with corticosteroids may result in elevated serum IgE concentrations. The ability of topical glucocorticoids to modulate the mucosal IgE response has not been elucidated. We studied the effect of topical steroid (fluticasone propionate) treatment on the local allergic antibody response induced by challenge with either allergen or diesel exhaust particles (DEP). A parallel group study was performed with ragweed-allergic subjects, each subject serving as his/her own control. Nasal provocation challenges were performed on three groups. One group received ragweed allergen, another diesel exhaust particles, and the third saline. The study was repeated following 1 week of treatment with intranasal fluticasone propionate. Each group received the same challenge as before. The concentrations of total immunoglobulins (IgE, IgG, IgA, and IgM), anti-ragweed antibody, IgE- and IgA-secreting cells, epsilon (epsilon) mRNA, and cytokine mRNAs (IL-2, -4, -5, -6, TNF-alpha, INF-gamma) were measured in nasal lavages performed before and at various time points after challenge. Treatment with fluticasone propionate for 7 days caused a decrease in the concentrations of nasal IgE protein, IgE-producing cells, total epsilon mRNA, and all the cytokine mRNAs tested. Furthermore, treatment with fluticasone propionate inhibited the production of allergen-specific IgE and cytokine mRNAs following challenge with ragweed antigen. However, fluticasone treatment did not significantly inhibit the enhancement of mucosal IgE production or cytokine mRNAs observed following nasal challenge with DEP. These results indicate that 1-week treatment with topical fluticasone propionate was effective in blocking local effects of allergen exposure but was unable to inhibit the adjuvant-like effect of DEP. Copyright 1999 Academic Press.
机译:糖皮质激素以多种方式阻断局部过敏反应。但是,研究还表明,糖皮质激素会增加体外IgE的合成,而皮质类固醇激素的治疗​​可能会导致血清IgE浓度升高。尚未阐明局部糖皮质激素调节粘膜IgE反应的能力。我们研究了局部类固醇(丙酸氟替卡松)治疗对由过敏原或柴油机尾气颗粒(DEP)激发引起的局部过敏抗体反应的影响。对豚草过敏性受试者进行了平行分组研究,每个受试者作为他/她自己的对照。对三组进行了鼻刺激挑战。一组接受豚草过敏原,另一组柴油机尾气颗粒和第三种盐水。鼻内丙酸氟替卡松治疗1周后重复了该研究。每个小组都收到与以前相同的挑战。总免疫球蛋白(IgE,IgG,IgA和IgM),抗豚草抗体,分泌IgE和IgA的细胞,ε(ε)mRNA和细胞因子mRNA(IL-2,-4,-5,-在攻击之前和之后的各个时间点,在洗鼻液中测量图6中的TNF-α,INF-γ。丙酸氟替卡松治疗7天导致鼻内IgE蛋白,产生IgE的细胞,总epsilon mRNA以及所有测试的细胞因子mRNA浓度降低。此外,用豚草抗原攻击后,丙酸氟替卡松治疗抑制了变应原特异性IgE和细胞因子mRNA的产生。但是,氟替卡松治疗并没有明显抑制DEP鼻腔攻击后观察到的粘膜IgE产生或细胞因子mRNA的增加。这些结果表明,局部使用丙酸氟替卡松治疗1周可有效阻止过敏原暴露的局部作用,但不能抑制DEP的佐剂样作用。版权所有1999,学术出版社。

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