Revez Joana A, Bain Lisa M, Watson Rick M, Towers Michelle, Collins Tina, Killian Kieran J, O'Byrne Paul M, Gauvreau Gail M, Upham John W, Ferreira Manuel Ar
QIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Division of Respirology Department of Medicine McMaster University Hamilton ON Canada.
Clin Transl Immunology. 2019 Jun 14;8(6):e1044. doi: 10.1002/cti2.1044. eCollection 2019.
Interleukin (IL)-6 signalling has been implicated in allergic asthma by animal, genetic association and clinical studies. In this study, we tested the hypothesis that tocilizumab (TCZ), a human monoclonal antibody that blocks IL-6 signalling, can prevent the development of allergen-induced bronchoconstriction in humans.
We performed a randomised, double-blind, placebo-controlled study, with eligible participants completing two allergen inhalation challenge tests, conducted before and after treatment with a single dose of TCZ or placebo. The primary efficacy endpoint was the magnitude of the late asthmatic response recorded between 3 and 7 after allergen challenge. The secondary efficacy endpoint was the early asthmatic response, measured 20 min to 2 h after allergen challenge.
A total of 66 patients enrolled between September 2014 and August 2017, when the trial was stopped for futility based on results from an interim analysis. Eleven patients fulfilled all eligibility criteria assessed at baseline and were subsequently randomised to the TCZ (=6) or placebo (=5) groups. Both the primary and secondary efficacy endpoints were not significantly different between the two groups. Five patients reported adverse events (AEs), three in the TCZ group (11 AEs) and two in the placebo group (four AEs). Only one AE was TCZ-related (mild neutropenia), and there were no serious AEs. Significant treatment effects were observed for serum levels of C-reactive protein, IL-6 and soluble IL-6R levels.
In a small proof-of-concept clinical trial, we found no evidence that a single dose of tocilizumab was able to prevent allergen-induced bronchoconstriction. (Trial registered in the Australian New Zealand Clinical Trials Registry, number ACTRN12614000123640).
动物、遗传关联和临床研究表明,白细胞介素(IL)-6信号传导与过敏性哮喘有关。在本研究中,我们检验了一种假设,即阻断IL-6信号传导的人单克隆抗体托珠单抗(TCZ)可预防人类变应原诱发的支气管收缩。
我们进行了一项随机、双盲、安慰剂对照研究,符合条件的参与者完成两次变应原吸入激发试验,分别在单剂量TCZ或安慰剂治疗前后进行。主要疗效终点是变应原激发后3至7小时记录的迟发性哮喘反应的程度。次要疗效终点是变应原激发后20分钟至2小时测量的早发性哮喘反应。
2014年9月至2017年8月期间共招募了66例患者,基于中期分析结果,该试验因无效而提前终止。11例患者符合基线评估的所有入选标准,随后被随机分为TCZ组(n = 6)或安慰剂组(n = 5)。两组的主要和次要疗效终点均无显著差异。5例患者报告了不良事件(AE),TCZ组3例(11次AE),安慰剂组2例(4次AE)。只有1次AE与TCZ相关(轻度中性粒细胞减少),且无严重AE。观察到血清C反应蛋白、IL-6和可溶性IL-6R水平有显著治疗效果。
在一项小型概念验证临床试验中,我们没有发现证据表明单剂量托珠单抗能够预防变应原诱发的支气管收缩。(该试验已在澳大利亚新西兰临床试验注册中心注册,注册号为ACTRN12614000123640)