Department of Pathology, University of North Dakota School of Medicine & Health Sciences, Grand Forks, ND, USA.
Department of Biomedical Sciences, University of North Dakota School of Medicine & Health Sciences, Grand Forks, ND, USA.
Methods Mol Biol. 2021;2223:159-167. doi: 10.1007/978-1-0716-1001-5_12.
Type-I hypersensitivity is commonly characterized by increased levels of antigen-specific immunoglobulin (Ig) E. Therefore, it is important for clinical and research investigators to reliably measure serum levels of IgE in allergic patients and animal models. While current ELISA-based methods are simple and commonly performed for the detection of allergen-specific IgE using serum or plasma, they may produce misleading results. This is in part due to decreased sensitivity for IgE in the presence of other Ig isotypes in the same sample, such as IgG, that are typically more abundant than IgE. When assessment of multiple Ig isotypes is necessary, performing optimized assays for individual isotypes requires high sample volumes. Here, we describe an approach to increase the sensitivity for IgE detection while conserving the sample volume needed. This method not only improves the accuracy of serum IgE measurements but also allows simultaneous analysis of other allergen-specific immunoglobulins.
I 型超敏反应的特征通常为抗原特异性免疫球蛋白 (Ig) E 水平升高。因此,对于临床和研究研究人员来说,可靠地测量过敏患者和动物模型中的血清 IgE 水平非常重要。虽然目前基于 ELISA 的方法简单且常用于使用血清或血浆检测过敏原特异性 IgE,但它们可能会产生误导性结果。这在一定程度上是由于在同一样本中存在其他 Ig 同种型(如 IgG)时,IgE 的敏感性降低,而 IgG 通常比 IgE 更丰富。当需要评估多种 Ig 同种型时,针对各个同种型进行优化检测需要大量的样本量。在这里,我们描述了一种在保留所需样本量的同时提高 IgE 检测灵敏度的方法。该方法不仅提高了血清 IgE 测量的准确性,而且还允许同时分析其他过敏原特异性免疫球蛋白。