Krefting Research Centre, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Wallenberg Centre for Molecular and Translational Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Krefting Research Centre, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Division of Allergology and Respiratory Medicine, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
J Allergy Clin Immunol Pract. 2019 Apr;7(4):1230-1238.e4. doi: 10.1016/j.jaip.2018.12.018. Epub 2018 Dec 27.
Sensitization to allergen components has been linked to asthma in children, but studies in adults are lacking.
To study the relation of sensitization to furry animal allergen components to risk of asthma, rhinitis, and markers of asthma severity in adults.
From the West Sweden Asthma Study, a random population-representative sample of adults aged 16 to 75 years, 2006 participants were clinically examined; 1872 were analyzed for serum IgE level to a mix of aeroallergens. Those with an IgE level of more than 0.35 kU/L to cat, dog, or horse allergen components were analyzed for specific cat (Felis domesticus [Fel d 1, Fel d 2, and Fel d 4]), dog (Canis familiaris [Can f 1, Can f 2, Can f 3, and Can f 5]), and horse (Equus caballus [Equ c 1]) allergen components. We defined monosensitization, double sensitization, and polysensitization (>2 components) patterns and applied cluster analysis to derive distinct sensitization clusters.
Sensitization to each allergen component, lipocalins, each sensitization pattern, and each sensitization cluster (nonsensitized, Fel d 1-driven sensitized, and multisensitized clusters) was associated with substantial increased risk of asthma, rhinitis, concomitant asthma and rhinitis, and Asthma Control Test-controlled asthma. Fel d 1, Can f 1, Can f 2, Can f 3, polysensitization, and multisensitized cluster were further associated with increased fractional exhaled nitric oxide and eosinophil levels, but with lower PD methacoline (provocative dose of methacholine causing a 20% drop in FEV) values. There was no association with asthma exacerbations, FEV predicted values, emergency visits or regular oral steroid use, and neutrophil levels.
Sensitization to furry animal allergen components is an important predictor of asthma, rhinitis, and markers of asthma severity with increased blood eosinophils, fractional exhaled nitric oxide, and airway hyperreactivity.
变应原成分致敏与儿童哮喘有关,但成人研究较少。
研究成人对皮毛动物变应原成分致敏与哮喘、鼻炎和哮喘严重程度标志物的关系。
来自于 2006 年的瑞典西部哮喘研究,这是一项针对 16 至 75 岁成年人的随机人群代表性研究,其中 2006 名参与者进行了临床检查;1872 名参与者分析了血清 IgE 水平对混合气传过敏原的反应。对 IgE 水平超过 0.35 kU/L 对猫、狗或马过敏原成分的人进行了特异性猫(家猫[Fel d 1、Fel d 2 和 Fel d 4])、狗(犬[Can f 1、Can f 2、Can f 3 和 Can f 5])和马(马[Equ c 1])过敏原成分的分析。我们定义了单敏、双敏和多敏(>2 种成分)模式,并应用聚类分析得出不同的致敏聚类。
对每种过敏原成分、脂质运载蛋白、每种致敏模式和每种致敏聚类(无致敏、Fel d 1 驱动致敏和多致敏聚类)的致敏与哮喘、鼻炎、哮喘和鼻炎同时存在、哮喘控制测试控制的哮喘的风险显著增加相关。Fel d 1、Can f 1、Can f 2、Can f 3、多敏和多敏聚类进一步与呼出气一氧化氮分数和嗜酸性粒细胞水平升高相关,但与较低的 PD 甲泼尼龙(引起 FEV 下降 20%的甲泼尼龙激发剂量)值相关。与哮喘恶化、FEV 预计值、急诊就诊或常规口服类固醇使用以及中性粒细胞水平无关。
对皮毛动物变应原成分的致敏是哮喘、鼻炎和哮喘严重程度标志物的重要预测因子,这些标志物与血液嗜酸性粒细胞增多、呼出气一氧化氮分数升高和气道高反应性有关。