Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Clin Exp Allergy. 2022 Oct;52(10):1169-1182. doi: 10.1111/cea.14176. Epub 2022 Jun 6.
Infection with rhinovirus (RV) is a major risk factor for disease exacerbations in patients with allergic asthma. This study analysed a broad set of cytokines in the noses of children and adults with asthma during RV infection in order to identify immunophenotypes that may link to virus-induced episodes.
Nasal wash specimens were analysed in children (n = 279 [healthy, n = 125; stable asthma, n = 64; wheeze, n = 90], ages 2-12) who presented to a hospital emergency department, and in adults (n = 44 [healthy, n = 13; asthma, n = 31], ages 18-38) who were experimentally infected with RV, including a subset who received anti-IgE. Cytokines were measured by multiplex bead assay and data analysed by univariate and multivariate methods to test relationships to viral load, allergic status, airway inflammation, and clinical outcomes.
Analysis of a core set of 7 cytokines (IL-6, CXCL8/IL-8, IL-15, EGF, G-CSF, CXCL10/IP-10 and CCL22/MDC) revealed higher levels in children with acute wheeze versus those with stable asthma or controls. Multivariate analysis identified two clusters that were enriched for acutely wheezing children; one displaying high viral load ("RV-high") with robust secretion of CXCL10, and the other displaying high IgE with elevated EGF, CXCL8 and both eosinophil- and neutrophil-derived mediators. Broader assessment of 39 cytokines confirmed that children with acute wheeze were not deficient in type 1 anti-viral responses. Analysis of 18 nasal cytokines in adults with asthma who received RV challenge identified two clusters; one that was "RV-high" and linked to robust induction of anti-viral cytokines and anti-IgE; and the other associated with more severe symptoms and a higher inflammatory state featuring eosinophil and neutrophil factors.
The results confirm the presence of different immunophenotypes linked to parameters of airway disease in both children and adults with asthma who are infected with RV. Such discrepancies may reflect the ability to regulate anti-viral responses.
鼻病毒 (RV) 感染是过敏性哮喘患者疾病恶化的主要危险因素。本研究分析了哮喘儿童和成人在 RV 感染期间广泛的细胞因子,以确定可能与病毒诱导发作相关的免疫表型。
分析了在医院急诊就诊的儿童(n=279[健康,n=125;稳定哮喘,n=64;喘息,n=90],年龄 2-12 岁)和接受 RV 实验感染的成人(n=44[健康,n=13;哮喘,n=31],年龄 18-38 岁)的鼻腔冲洗标本,其中包括接受抗 IgE 治疗的亚组。通过多重微珠检测法测量细胞因子,并通过单变量和多变量方法分析数据,以测试与病毒载量、过敏状态、气道炎症和临床结局的关系。
对 7 种细胞因子(IL-6、CXCL8/IL-8、IL-15、EGF、G-CSF、CXCL10/IP-10 和 CCL22/MDC)的核心集进行分析显示,急性喘息儿童的水平高于稳定哮喘或对照儿童。多变量分析确定了两个富含急性喘息儿童的聚类;一个显示高病毒载量(“RV 高”),具有强烈的 CXCL10 分泌,另一个显示高 IgE,具有升高的 EGF、CXCL8 以及嗜酸性粒细胞和中性粒细胞衍生的介质。对 39 种细胞因子的广泛评估证实,急性喘息儿童并不缺乏 1 型抗病毒反应。对接受 RV 挑战的哮喘成人的 18 种鼻细胞因子进行分析,确定了两个聚类;一个是“RV 高”,与强烈诱导抗病毒细胞因子和抗 IgE 相关;另一个与更严重的症状相关,具有更高的炎症状态,表现为嗜酸性粒细胞和中性粒细胞因子。
这些结果证实,在感染 RV 的儿童和成人哮喘患者中,存在与气道疾病参数相关的不同免疫表型。这种差异可能反映了调节抗病毒反应的能力。