首页> 外文期刊>The Lancet >Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response.
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Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response.

机译:白介素5阻断单克隆抗体对嗜酸性粒细胞,气道高反应性和晚期哮喘反应的影响。

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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.
机译:背景:白细胞介素5(IL-5)对于嗜酸性粒细胞的形成至关重要,嗜酸性粒细胞被认为在哮喘和其他过敏性疾病的发病机理中起着重要作用。我们旨在评估针对IL-5的单克隆抗体对轻度哮喘患者血液和痰中嗜酸性粒细胞,气道高反应性以及对吸入性过敏原的晚期哮喘反应的影响。方法:我们进行了一项双盲随机安慰剂对照试验,以2.5 mg / kg的剂量单次静脉输注人源化针对IL-5的人源化(IgG-K)单克隆抗体(SB-240563)(n = 8)或10.0 mg / kg(n = 8)。在第1和第4周测量治疗对吸入性变应原刺激反应,痰中嗜酸性粒细胞和气道对组胺高反应性的影响,并监测多达16周的血液嗜酸性粒细胞计数。结果:针对IL-5的单克隆抗体在第29天将平均血嗜酸性粒细胞计数从安慰剂组的0.25x10(9)/ L(95%CI 0.16-0.34)降低至0.04x10(9)/ L(0.00-0.07)在10 mg / kg组中(p <0.0001),并防止了过敏原激发后的血液嗜酸性粒细胞增多。吸入过敏原后,治疗后9天,安慰剂组的痰中嗜酸性粒细胞百分比为12.2%,而10 mg / kg组的痰中嗜酸性粒细胞百分比降至0.9%(-1.2至3.0; p = 0.0076),并且这种效果持续到一天服药后30。 IL-5单克隆抗体对晚期哮喘反应或对组胺的气道高反应性没有显着影响。解释:单剂抗IL-5单克隆抗体可减少长达16周的血液嗜酸性粒细胞,并在4周减少痰嗜酸性粒细胞,对哮喘和过敏具有相当大的治疗潜力。然而,我们的发现质疑嗜酸性粒细胞在介导晚期哮喘反应和引起气道高反应性中的作用。

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