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使用过敏原暴露室对过敏性鼻炎患者进行症状评估。

Symptom Assessment of Patients with Allergic Rhinitis Using an Allergen Exposure Chamber.

作者信息

Zemelka-Wiacek Magdalena, Kosowska Anna, Jutel Marek

机构信息

Department of Clinical Immunology, Wroclaw Medical University;

Department of Clinical Immunology, Wroclaw Medical University; ALL-MED Medical Research Institute.

出版信息

J Vis Exp. 2023 Mar 3(193). doi: 10.3791/64801.

Abstract

Allergen exposure chambers (AECs) are clinical facilities that allow the exposure of participants to allergenic and non-allergenic airborne particles. They provide stable particle concentrations under controlled environmental conditions. This is of great importance both for diagnostic purposes and for the monitoring of treatment effects. Here, a protocol and the technical prerequisites for performing a safe and effective allergen challenge in subjects sensitized to airborne allergens (i.e., house dust mite [HDM]) in the ALL-MED AEC are presented. With this method, triggering allergic symptoms corresponds to natural exposure. This can be used for an allergy diagnosis or as a plausible endpoint in clinical trials, particularly for allergen immunotherapy (AIT). A controlled environment (temperature, humidity, and carbon dioxide [CO2]) in the chamber must be maintained. Allergen particles must be dispersed evenly within the AEC at stable levels throughout the challenge. For this presentation, allergic rhinitis (AR) patients sensitive to HDM allergens were enrolled. AR symptoms were assessed by the following parameters: total nasal symptom score (TNSS), acoustic rhinometry (ARM), peak nasal inspiratory flow (PNIF), and nasal secretion weight. The safety of the procedure was assessed by the peak expiratory flow rate (PEFR) and the forced expiratory volume in the first second (FEV1). The allergic subjects developed symptoms within 120 min of the trial. On average, the most intense symptoms appeared after 60-90 min and, after reaching a plateau, remained stable until the end of the trial.

摘要

变应原暴露舱(AECs)是一种临床设施,可使参与者暴露于变应原性和非变应原性空气传播颗粒中。它们在可控的环境条件下提供稳定的颗粒浓度。这对于诊断目的和治疗效果监测都非常重要。在此,介绍了在ALL-MED AEC中对空气传播变应原(即屋尘螨[HDM])致敏的受试者进行安全有效的变应原激发试验的方案和技术前提条件。通过这种方法,引发过敏症状相当于自然暴露。这可用于过敏诊断或作为临床试验中似是而非的终点,特别是用于变应原免疫疗法(AIT)。必须维持舱内的可控环境(温度、湿度和二氧化碳[CO2])。在整个激发试验过程中,变应原颗粒必须在AEC内以稳定水平均匀分散。为了本次展示,招募了对HDM变应原敏感的变应性鼻炎(AR)患者。通过以下参数评估AR症状:总鼻症状评分(TNSS)、鼻声反射(ARM)、最大鼻吸气流量(PNIF)和鼻分泌物重量。通过呼气峰值流速(PEFR)和第一秒用力呼气量(FEV1)评估该程序的安全性。变应性受试者在试验的120分钟内出现症状。平均而言,最强烈的症状在60 - 90分钟后出现,达到平台期后,直至试验结束保持稳定。

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