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白介素-5给药治疗哮喘的全身而非肺部效应的证据。

Evidence for systemic rather than pulmonary effects of interleukin-5 administration in asthma.

作者信息

van Rensen E L, Stirling R G, Scheerens J, Staples K, Sterk P J, Barnes P J, Chung K F

机构信息

Department of Thoracic Medicine, National Heart and Lung Institute, Imperial College School of Medicine, London SW3 6LY, UK.

出版信息

Thorax. 2001 Dec;56(12):935-40. doi: 10.1136/thorax.56.12.935.

DOI:10.1136/thorax.56.12.935
PMID:11713356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1745987/
Abstract

BACKGROUND

Interleukin 5 (IL-5) has an important role in mobilisation of eosinophils from the bone marrow and in their subsequent terminal differentiation. A study was undertaken to determine whether inhaled and intravenous IL-5 could induce pulmonary eosinophilia and bronchial hyperresponsiveness (BHR) independently of these effects.

METHODS

Nine mild asthmatics received inhaled (15 microg) or intravenous (2 microg) IL-5 or placebo in random order in a double blind, crossover study. Blood samples were taken before and at 0.5, 1, 2, 3, 4, 5, 24, and 72 hours following IL-5 or placebo, and bronchial responsiveness (PC(20) methacholine) and eosinophil counts in induced sputum were determined.

RESULTS

Serum IL-5 levels were markedly increased 30 minutes after intravenous IL-5 (p=0.002), and sputum IL-5 levels increased 4 and 24 hours after inhaled IL-5 (p<0.05). Serum eotaxin was raised 24 hours after intravenous IL-5 but not after inhaled IL-5 or placebo. Blood eosinophils were markedly reduced 0.5-2 hours after intravenous IL-5 (p<0.05), followed by an increase at 3, 4, 5, and 72 hours (p<0.05). Sputum eosinophils rose significantly in all three groups at 24 hours but there were no differences between the groups. Bronchial responsiveness was not affected by IL-5.

CONCLUSION

The effects of IL-5 appear to be mainly in the circulation, inducing peripheral mobilisation of eosinophils to the circulation without any effect on eosinophil mobilisation in the lungs or on bronchial responsiveness.

摘要

背景

白细胞介素5(IL-5)在骨髓中嗜酸性粒细胞的动员及其随后的终末分化过程中发挥重要作用。本研究旨在确定吸入和静脉注射IL-5是否能独立于这些作用诱导肺部嗜酸性粒细胞增多和支气管高反应性(BHR)。

方法

在一项双盲交叉研究中,9名轻度哮喘患者随机依次接受吸入(15微克)或静脉注射(2微克)IL-5或安慰剂。在给予IL-5或安慰剂之前以及之后的0.5、1、2、3、4、5、24和72小时采集血样,并测定支气管反应性(乙酰甲胆碱PC20)和诱导痰中的嗜酸性粒细胞计数。

结果

静脉注射IL-5后30分钟血清IL-5水平显著升高(p = 0.002),吸入IL-5后4小时和24小时痰中IL-5水平升高(p < 0.05)。静脉注射IL-5后24小时血清嗜酸性粒细胞趋化因子升高,但吸入IL-5或安慰剂后未升高。静脉注射IL-5后0.5 - 2小时血嗜酸性粒细胞显著减少(p < 0.05),随后在3、4、5和72小时升高(p < 0.05)。所有三组在24小时时痰嗜酸性粒细胞均显著升高,但组间无差异。支气管反应性不受IL-5影响。

结论

IL-5的作用似乎主要在循环系统,诱导嗜酸性粒细胞从外周动员至循环系统,而对肺部嗜酸性粒细胞的动员或支气管反应性无任何影响。

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