Department of Paediatric Pneumology & Immunology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
J Allergy Clin Immunol. 2017 Feb;139(2):541-549.e8. doi: 10.1016/j.jaci.2016.08.014. Epub 2016 Oct 25.
The evolution of the IgE response to the numerous allergen molecules of Dermatophagoides pteronyssinus is still unknown.
We sought to characterize the evolutionary patterns of the IgE response to 12 molecules of D pteronyssinus from birth to adulthood and to investigate their determinants and clinical relevance.
We investigated the clinical data and sera of 722 participants in the German Multicenter Allergy Study, a birth cohort started in 1990. Diagnoses of current allergic rhinitis (AR) related to mite allergy and asthma were based on yearly interviews at the ages of 1 to 13 years and 20 years. IgE to the extract and 12 molecules of D pteronyssinus were tested by means of ImmunoCAP and microarray technology, respectively, in sera collected at ages 1, 2, 3, 5, 6, 7, 10, 13, and 20 years. Exposure to mites at age 6 and 18 months was assessed by measuring Der p 1 weight/weight concentration in house dust.
One hundred ninety-one (26.5%) of 722 participants ever had IgE to D pteronyssinus extract (≥0.35 kU/L). At age 20 years, their IgE recognized most frequently Der p 2, Der p 1, and Der p 23 (group A molecules; prevalence, >40%), followed by Der p 5, Der p 7, Der p 4, and Der p 21 (group B molecules; prevalence, 15% to 30%) and Der p 11, Der p 18, clone 16, Der p 14, and Der p 15 (group C molecules; prevalence, <10%). IgE sensitization started almost invariably with group A molecules and expanded sequentially first to group B and finally to group C molecules. Early IgE sensitization onset, parental hay fever, and higher exposure to mites were associated with a broader polymolecular IgE sensitization pattern. Participants reaching the broadest IgE sensitization stage (ie, ABC) had significantly higher risk of mite-related AR and asthma than unsensitized participants. IgE to Der p 1 or Der p 23 at age 5 years or less predicted asthma at school age.
Parental hay fever and early exposure to D pteronyssinus allergens promote IgE polysensitization to several D pteronyssinus molecules, which in turn predicts current mite-related AR and current/future asthma. These results might inspire predictive algorithms and prevention strategies against the progression of IgE sensitization to mites toward AR and asthma.
目前尚不清楚尘螨过敏原分子的 IgE 反应的演变过程。
我们旨在描述从出生到成年期间对 12 种尘螨蛋白的 IgE 反应的进化模式,并研究其决定因素和临床相关性。
我们调查了德国多中心过敏研究中的 722 名参与者的临床数据和血清,该研究是 1990 年开始的一项出生队列研究。根据 1 至 13 岁和 20 岁时每年的访谈,诊断当前与尘螨过敏相关的过敏性鼻炎 (AR) 和哮喘。通过 ImmunoCAP 和微阵列技术分别检测尘螨提取物和 12 种尘螨蛋白的 IgE,血清样本采集于 1、2、3、5、6、7、10、13 和 20 岁。通过测量屋尘中 Der p 1 重量/重量浓度来评估 6 个月和 18 个月时的螨暴露情况。
722 名参与者中有 191 名(26.5%)曾对尘螨提取物产生 IgE(≥0.35 kU/L)。在 20 岁时,他们的 IgE 最常识别 Der p 2、Der p 1 和 Der p 23(A 组分子;患病率>40%),其次是 Der p 5、Der p 7、Der p 4 和 Der p 21(B 组分子;患病率 15%至 30%)和 Der p 11、Der p 18、克隆 16、Der p 14 和 Der p 15(C 组分子;患病率<10%)。IgE 致敏几乎总是从 A 组分子开始,并首先依次扩展到 B 组,最后扩展到 C 组分子。早期 IgE 致敏的起始、父母的花粉热和更高的螨暴露与更广泛的多分子 IgE 致敏模式相关。达到最广泛的 IgE 致敏阶段(即 ABC)的参与者患与螨相关的 AR 和哮喘的风险明显高于未致敏的参与者。5 岁或以下时的 Der p 1 或 Der p 23 的 IgE 预测学龄时的哮喘。
父母的花粉热和早期接触尘螨过敏原会促进对几种尘螨分子的 IgE 多敏化,进而预测当前与尘螨相关的 AR 和当前/未来的哮喘。这些结果可能会激发针对 IgE 对尘螨过敏向 AR 和哮喘进展的预测算法和预防策略。