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白细胞介素-5阻断单克隆抗体对嗜酸性粒细胞、气道高反应性和哮喘迟发反应的影响。

Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response.

作者信息

Leckie M J, ten Brinke A, Khan J, Diamant Z, O'Connor B J, Walls C M, Mathur A K, Cowley H C, Chung K F, Djukanovic R, Hansel T T, Holgate S T, Sterk P J, Barnes P J

机构信息

National Heart and Lung Institute, Imperial College, London, UK.

出版信息

Lancet. 2000;356(9248):2144-8. doi: 10.1016/s0140-6736(00)03496-6.

Abstract

BACKGROUND

Interleukin-5 (IL-5) is essential for the formation of eosinophils, which are thought to have a major role in the pathogenesis of asthma and other allergic diseases. We aimed to assess the effects of monoclonal antibody to IL-5 on blood and sputum eosinophils, airway hyper-responsiveness, and the late asthmatic reaction to inhaled allergen in patients with mild asthma.

METHODS

We did a double-blind randomised placebo-controlled trial, in which a single intravenous infusion of humanised (IgG-K) monoclonal antibody to IL-5 (SB-240563) was given at doses of 2.5 mg/kg (n=8) or 10.0 mg/kg (n=8). The effects of treatment on responses to inhaled allergen challenge, sputum eosinophils, and airway hyper-responsiveness to histamine were measured at weeks 1 and 4 with monitoring of blood eosinophil counts for up to 16 weeks.

FINDINGS

Monoclonal antibody against IL-5 lowered the mean blood eosinophil count at day 29 from 0.25x10(9)/L (95% CI 0.16-0.34) in the placebo group to 0.04x10(9)/L (0.00-0.07) in the 10 mg/kg group (p<0.0001), and prevented the blood eosinophilia that follows allergen challenge. After inhaled allergen challenge, 9 days after treatment, the percentage sputum eosinophils were 12.2% in the placebo group and lowered to 0.9% (-1.2 to 3.0; p=0.0076) in the 10 mg/kg group, and this effect persisted at day 30 after the dose. There was no significant effect of monoclonal antibody to IL-5 on the late asthmatic response or on airway hyper-responsiveness to histamine.

INTERPRETATION

A single dose of monoclonal antibody to IL-5 decreased blood eosinophils for up to 16 weeks and sputum eosinophils at 4 weeks, which has considerable therapeutic potential for asthma and allergy. However, our findings question the role of eosinophils in mediating the late asthmatic response and causing airway hyper-responsiveness.

摘要

背景

白细胞介素-5(IL-5)对嗜酸性粒细胞的形成至关重要,而嗜酸性粒细胞被认为在哮喘和其他过敏性疾病的发病机制中起主要作用。我们旨在评估抗IL-5单克隆抗体对轻度哮喘患者血液和痰液嗜酸性粒细胞、气道高反应性以及对吸入变应原的迟发性哮喘反应的影响。

方法

我们进行了一项双盲随机安慰剂对照试验,其中以2.5mg/kg(n = 8)或10.0mg/kg(n = 8)的剂量单次静脉输注人源化(IgG-K)抗IL-5单克隆抗体(SB - 240563)。在第1周和第4周测量治疗对吸入变应原激发反应、痰液嗜酸性粒细胞以及对组胺的气道高反应性的影响,并监测血液嗜酸性粒细胞计数长达16周。

结果

抗IL-5单克隆抗体使第29天的平均血液嗜酸性粒细胞计数从安慰剂组的0.25×10⁹/L(95%CI 0.16 - 0.34)降至10mg/kg组的0.04×10⁹/L(0.00 - 0.07)(p<0.0001),并预防了变应原激发后的血液嗜酸性粒细胞增多。吸入变应原激发后,治疗9天后,安慰剂组痰液嗜酸性粒细胞百分比为12.2%,而10mg/kg组降至0.9%(-1.2至3.0;p = 0.0076),且该效应在给药后第30天持续存在。抗IL-5单克隆抗体对迟发性哮喘反应或对组胺的气道高反应性无显著影响。

解读

单剂量抗IL-5单克隆抗体可使血液嗜酸性粒细胞减少长达16周,痰液嗜酸性粒细胞在4周时减少,这对哮喘和过敏具有相当大的治疗潜力。然而,我们的研究结果对嗜酸性粒细胞在介导迟发性哮喘反应和引起气道高反应性中的作用提出了质疑。

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