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变应性鼻炎临床研究者协作组(AR-CIC):在一项使用针对猫过敏的研究性免疫疗法的研究中对鼻过敏原激发程序的验证。

The Allergic Rhinitis Clinical Investigator Collaborative (AR-CIC): verification of nasal allergen challenge procedures in a study utilizing an investigational immunotherapy for cat allergy.

作者信息

Neighbour Helen, Soliman Mena, Steacy Lisa M, Hickey Pascal, Forbes Beth, Larché Mark, Ellis Anne K

机构信息

1Divisions of Clinical Immunology & Allergy and Respirology, Department of Medicine, Firestone Institute of Respiratory Health, The Research Institute, St. Joe's Hamilton and McMaster University, Hamilton, ON Canada.

2Allergy Research Unit, Kingston General Hospital, Kingston, ON Canada.

出版信息

Clin Transl Allergy. 2018 Apr 12;8:15. doi: 10.1186/s13601-018-0198-7. eCollection 2018.

Abstract

BACKGROUND

The Allergic Rhinitis Clinical Investigator Collaborative (AR-CIC) is a network of experienced Allergic Rhinitis (AR) researchers developing better research tools based on the nasal allergen challenge (NAC). A key objective of such is the ability to detect efficacy in a small population. AR-CIC sought to test its NAC protocol as a secondary objective in two small mechanistic research trials of a novel form of immunotherapy [Cat Peptide Antigen Desensitisation (Cat-PAD)] for which efficacy had previously been demonstrated. The primary objective (not presented here) was to identify potential biomarkers of efficacy for peptide immunotherapy, and this provided an ideal opportunity to corroborate the NAC protocol. We aim to clinically validate the AR-CIC NAC methodology in a pooled analysis of secondary endpoints measured in two open label mechanistic studies of cat allergic participants treated with Cat-PAD.

METHODS

Cat allergic AR sufferers with ongoing cat exposure were included. Participants had to demonstrate a total nasal symptom score (TNSS) of at least 8 (max 12) and/or achieve a reduction in peak nasal inspiratory flow (PNIF) of ≥ 50% during a screening titrated NAC. Eligible participants then underwent a baseline NAC visit with the allergen dose that produced a positive challenge at screening, followed by four monthly injections of 6 nmol Cat-PAD. A follow up NAC visit documented changes in nasal response 1 month following the completion of treatment.

RESULTS

Nineteen subjects completed the study protocol in the two studies combined. Four injections of Cat-PAD resulted in a significant reduction in TNSS responses generated via NAC following allergen challenge (15 min  < 0.05, 30 min  < 0.05, 1 h  < 0.01, 2 h  < 0.05). There was modest correlation between symptom scores and PNIF measurements.

CONCLUSIONS

This study supports the validity of the AR-CIC's optimised NAC protocol for conducting research of the potential efficacy of novel therapeutics in multi-centre studies. Both studies reported herein were registered clinicaltrials.gov (NCT01383590 and NCT01383603).

摘要

背景

变应性鼻炎临床研究者协作组(AR-CIC)是一个由经验丰富的变应性鼻炎(AR)研究人员组成的网络,旨在基于鼻过敏原激发试验(NAC)开发更好的研究工具。其一个关键目标是能够在小样本人群中检测疗效。AR-CIC试图在两项小型机制性研究中,将其NAC方案作为次要目标进行测试,这两项研究针对一种新型免疫疗法[猫肽抗原脱敏疗法(Cat-PAD)],该疗法此前已证明具有疗效。主要目标(此处未展示)是确定肽免疫疗法疗效的潜在生物标志物,这为验证NAC方案提供了理想机会。我们旨在通过对两项开放标签机制性研究中接受Cat-PAD治疗的猫过敏参与者的次要终点进行汇总分析,从临床角度验证AR-CIC的NAC方法。

方法

纳入持续接触猫的猫过敏AR患者。参与者在筛选滴定NAC期间,总鼻症状评分(TNSS)必须至少为8(满分12)和/或鼻吸气峰流速(PNIF)降低≥50%。符合条件的参与者随后接受一次基线NAC访视,使用在筛选时产生阳性激发的过敏原剂量,然后每月注射4次6 nmol的Cat-PAD。治疗完成后1个月的随访NAC访视记录了鼻反应的变化。

结果

两项研究合并后,19名受试者完成了研究方案。4次注射Cat-PAD导致过敏原激发后通过NAC产生的TNSS反应显著降低(15分钟<0.05,30分钟<0.05,1小时<0.01,2小时<0.05)。症状评分与PNIF测量之间存在适度相关性。

结论

本研究支持AR-CIC优化的NAC方案在多中心研究中对新型疗法潜在疗效进行研究的有效性。本文报道的两项研究均已在clinicaltrials.gov注册(NCT01383590和NCT01383603)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2809/5896125/77cb0bd0789f/13601_2018_198_Fig1_HTML.jpg

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