Haldar Pranabashis, Brightling Christopher E, Hargadon Beverley, Gupta Sumit, Monteiro William, Sousa Ana, Marshall Richard P, Bradding Peter, Green Ruth H, Wardlaw Andrew J, Pavord Ian D
Institute for Lung Health, Glenfield Hospital, University Hospitals of Leicester National Health Service Trust, Leicester, United Kingdom.
N Engl J Med. 2009 Mar 5;360(10):973-84. doi: 10.1056/NEJMoa0808991.
Exacerbations of asthma are associated with substantial morbidity and mortality and with considerable use of health care resources. Preventing exacerbations remains an important goal of therapy. There is evidence that eosinophilic inflammation of the airway is associated with the risk of exacerbations.
We conducted a randomized, double-blind, placebo-controlled, parallel-group study of 61 subjects who had refractory eosinophilic asthma and a history of recurrent severe exacerbations. Subjects received infusions of either mepolizumab, an anti-interleukin-5 monoclonal antibody (29 subjects), or placebo (32) at monthly intervals for 1 year. The primary outcome measure was the number of severe exacerbations per subject during the 50-week treatment phase. Secondary outcomes included a change in asthma symptoms, scores on the Asthma Quality of Life Questionnaire (AQLQ, in which scores range from 1 to 7, with lower values indicating more severe impairment and a change of 0.5 unit considered to be clinically important), forced expiratory volume in 1 second (FEV(1)) after use of a bronchodilator, airway hyperresponsiveness, and eosinophil counts in the blood and sputum.
Mepolizumab was associated with significantly fewer severe exacerbations than placebo over the course of 50 weeks (2.0 vs. 3.4 mean exacerbations per subject; relative risk, 0.57; 95% confidence interval [CI], 0.32 to 0.92; P=0.02) and with a significant improvement in the score on the AQLQ (mean increase from baseline, 0.55 vs. 0.19; mean difference between groups, 0.35; 95% CI, 0.08 to 0.62; P=0.02). Mepolizumab significantly lowered eosinophil counts in the blood (P<0.001) and sputum (P=0.002). There were no significant differences between the groups with respect to symptoms, FEV(1) after bronchodilator use, or airway hyperresponsiveness. The only serious adverse events reported were hospitalizations for acute severe asthma.
Mepolizumab therapy reduces exacerbations and improves AQLQ scores in patients with refractory eosinophilic asthma. The results of our study suggest that eosinophils have a role as important effector cells in the pathogenesis of severe exacerbations of asthma in this patient population. (Current Controlled Trials number, ISRCTN75169762.)
哮喘急性发作与严重的发病率和死亡率相关,且医疗资源使用量可观。预防急性发作仍然是治疗的一个重要目标。有证据表明气道嗜酸性粒细胞炎症与急性发作风险相关。
我们对61名患有难治性嗜酸性粒细胞哮喘且有反复严重急性发作病史的受试者进行了一项随机、双盲、安慰剂对照的平行组研究。受试者每月接受一次美泊利单抗(一种抗白细胞介素-5单克隆抗体,29名受试者)或安慰剂(32名受试者)输注,持续1年。主要结局指标是在50周治疗阶段每位受试者的严重急性发作次数。次要结局包括哮喘症状的变化、哮喘生活质量问卷(AQLQ,评分范围为1至7,分数越低表明损害越严重,0.5分的变化被认为具有临床意义)的得分、使用支气管扩张剂后1秒用力呼气量(FEV₁)、气道高反应性以及血液和痰液中的嗜酸性粒细胞计数。
在50周的疗程中,美泊利单抗组的严重急性发作次数显著少于安慰剂组(每位受试者平均发作次数分别为2.0次和3.4次;相对风险为0.57;95%置信区间[CI]为0.32至0.92;P = 0.02),且AQLQ评分有显著改善(与基线相比平均增加0.55分,而安慰剂组为0.19分;组间平均差异为0.35分;95%CI为0.08至0.62;P = 0.02)。美泊利单抗显著降低了血液(P < 0.001)和痰液(P = 0.002)中的嗜酸性粒细胞计数。两组在症状、使用支气管扩张剂后的FEV₁或气道高反应性方面无显著差异。报告的唯一严重不良事件是急性重症哮喘住院。
美泊利单抗治疗可减少难治性嗜酸性粒细胞哮喘患者的急性发作次数并改善AQLQ评分。我们的研究结果表明,嗜酸性粒细胞在该患者群体严重哮喘急性发作的发病机制中作为重要效应细胞发挥作用。(当前对照试验编号,ISRCTN75169762。)