Dehus Oliver, Zimmer Julia, Döring Sascha, Führer Frank, Hanschmann Kay-Martin, Holzhauser Thomas, Neske Florian, Strecker Daniel, Trösemeier Jan-Hendrik, Vieths Stefan, Kaul Susanne
Division of Allergology, Paul-Ehrlich-Institut, Paul-Ehrlich-Straße 51-59, 63225, Langen, Germany.
Anal Bioanal Chem. 2015 Feb;407(6):1673-83. doi: 10.1007/s00216-014-8418-z. Epub 2015 Jan 9.
Birch (Betula) pollen is a major cause of allergy in northern and central Europe. The allergenic potency of products for diagnosis and therapy of birch pollen allergy is adjusted nearly exclusively to the major birch pollen allergen Bet v 1. Although every fifth patient is additionally sensitized to Bet v 4, both content and variability of this minor allergen in birch allergen products remain unclear due to a lack of simple and cost-effective quantitative methods. This study aimed to develop and in-house validate the first Bet v 4-specific sandwich enzyme-linked immunosorbent assay (ELISA). Based on a murine monoclonal antibody in combination with a polyclonal rabbit antiserum, the ELISA proved to be highly sensitive, with a lower limit of quantification of 30 pg/ml Bet v 4. After confirmation of satisfactory accuracy, reproducibility, and robustness, the ELISA was utilized to quantify Bet v 4 in 30 authorized birch allergen products. The allergen was detected in all samples tested, ranging from 0.2 to 4.4 μg/ml. No significant correlation of Bet v 4 was found with the respective amount of Bet v 1. In contrast to Bet v 1, also no correlation of Bet v 4 with total protein content or total allergenic activity could be observed. Thus, it seems presently unfeasible to base birch allergen product standardization additionally on Bet v 4. In light of these results, the continuous monitoring of Bet v 4 in birch allergen products with the presented ELISA will provide a basis for the understanding of the clinical relevance of minor allergens.
桦树(Betula)花粉是北欧和中欧过敏的主要原因。用于桦树花粉过敏诊断和治疗的产品的致敏效力几乎完全根据主要的桦树花粉过敏原Bet v 1进行调整。尽管每五名患者中就有一名还对Bet v 4致敏,但由于缺乏简单且经济高效的定量方法,这种次要过敏原在桦树过敏原产品中的含量和变异性仍不清楚。本研究旨在开发并在内部验证首个Bet v 4特异性夹心酶联免疫吸附测定(ELISA)。基于鼠单克隆抗体与兔多克隆抗血清的组合,该ELISA被证明具有高度敏感性,Bet v 4的定量下限为30 pg/ml。在确认具有令人满意的准确性、重现性和稳健性后,该ELISA被用于定量30种获批的桦树过敏原产品中的Bet v 4。在所有测试样品中均检测到该过敏原,含量范围为0.2至4.4 μg/ml。未发现Bet v 4与相应的Bet v 1含量之间存在显著相关性。与Bet v 1不同,也未观察到Bet v 4与总蛋白含量或总致敏活性之间存在相关性。因此,目前似乎无法额外基于Bet v 4对桦树过敏原产品进行标准化。鉴于这些结果,使用所提出的ELISA持续监测桦树过敏原产品中的Bet v 4将为理解次要过敏原的临床相关性提供基础。