Dr von Hauner Children's Hospital, LMU Munich, Munich, Germany.
Dr von Hauner Children's Hospital, LMU Munich, Munich, Germany.
J Allergy Clin Immunol. 2017 Jun;139(6):1935-1945.e12. doi: 10.1016/j.jaci.2016.08.046. Epub 2016 Oct 19.
Phenotypes of childhood-onset asthma are characterized by distinct trajectories and functional features. For atopy, definition of phenotypes during childhood is less clear.
We sought to define phenotypes of atopic sensitization over the first 6 years of life using a latent class analysis (LCA) integrating 3 dimensions of atopy: allergen specificity, time course, and levels of specific IgE (sIgE).
Phenotypes were defined by means of LCA in 680 children of the Multizentrische Allergiestudie (MAS) and 766 children of the Protection against allergy: Study in Rural Environments (PASTURE) birth cohorts and compared with classical nondisjunctive definitions of seasonal, perennial, and food sensitization with respect to atopic diseases and lung function. Cytokine levels were measured in the PASTURE cohort.
The LCA classified predominantly by type and multiplicity of sensitization (food vs inhalant), allergen combinations, and sIgE levels. Latent classes were related to atopic disease manifestations with higher sensitivity and specificity than the classical definitions. LCA detected consistently in both cohorts a distinct group of children with severe atopy characterized by high seasonal sIgE levels and a strong propensity for asthma; hay fever; eczema; and impaired lung function, also in children without an established asthma diagnosis. Severe atopy was associated with an increased IL-5/IFN-γ ratio. A path analysis among sensitized children revealed that among all features of severe atopy, only excessive sIgE production early in life affected asthma risk.
LCA revealed a set of benign, symptomatic, and severe atopy phenotypes. The severe phenotype emerged as a latent condition with signs of a dysbalanced immune response. It determined high asthma risk through excessive sIgE production and directly affected impaired lung function.
儿童期起病哮喘的表型特征为明显的轨迹和功能特征。对于特应性,儿童时期表型的定义不太明确。
我们试图通过整合特应性的 3 个维度(过敏原特异性、时间进程和特异性 IgE [sIgE] 水平)的潜在类别分析(LCA),在儿童生命的头 6 年定义特应性致敏的表型。
通过 LCA 在 Multizentrische Allergiestudie(MAS)的 680 名儿童和 Protection against allergy: Study in Rural Environments(PASTURE)出生队列的 766 名儿童中定义表型,并与季节性、常年性和食物致敏的经典非分离定义进行比较,比较内容为特应性疾病和肺功能。在 PASTURE 队列中测量细胞因子水平。
LCA 主要根据致敏类型和多发性(食物与吸入性)、过敏原组合和 sIgE 水平进行分类。潜在类别与特应性疾病表现相关,具有比经典定义更高的敏感性和特异性。在两个队列中,LCA 均一致检测到一组具有严重特应性的儿童,其特征为高季节性 sIgE 水平和强烈的哮喘倾向;花粉症;湿疹;以及肺功能受损,即使在未确诊哮喘的儿童中也是如此。严重特应性与增加的 IL-5/IFN-γ 比值相关。在致敏儿童中进行的路径分析表明,在严重特应性的所有特征中,只有早期生活中过多的 sIgE 产生会影响哮喘风险。
LCA 揭示了一组良性、有症状和严重的特应性表型。严重表型是一种潜在的状态,具有免疫反应失衡的迹象。它通过过度的 sIgE 产生确定了高哮喘风险,并直接影响受损的肺功能。