首页> 美国卫生研究院文献>The Korean Journal of Parasitology >Monoclonal antibodies to recombinant Der p 2 a major house dust mite allergen: specificity epitope analysis and development of two-site capture ELISA
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Monoclonal antibodies to recombinant Der p 2 a major house dust mite allergen: specificity epitope analysis and development of two-site capture ELISA

机译:重组Der p 2(一种主要的屋尘螨过敏原)的单克隆抗体:特异性抗原决定簇分析和两点捕获ELISA的发展

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摘要

House dust mite allergens have been well established as sensitizing agents that are important in the induction of allergic diseases. In order to analyze epitopes of the allergen and to develop a quantitative method of the allergen exposure, monoclonal antibodies against a recombinant Der p 2 (rDer p 2), one of the major allergens of Dermatophagoides pteronyssinus, were produced. Four monoclonal antibodies produced were species-specific and did not cross-react to the D. farinae crude extract. Two of the monoclonal antibodies were found to be IgG1 and the others were IgM. For the analysis of epitopes, a Der p 2 cDNA encoding 126 amino acids (aa) was dissected into three fragments with several overlapping peptides, A (aa residues 1-49), B (44-93), and C fragment (84-126). Three monoclonal antibodies showed reactivities to the recombinant B fragment and to the full-length rDer p 2, but one monoclonal antibody reacted only with the full-length rDer p 2. Two-site capture ELISA was developed using two different monoclonal antibodies for quantitating Der p 2 in house dust. The sensitivity limit was 4 ng/ml with rDer p 2 and 8 µg/ml with the D. pteronyssinus crude extract. The result suggested that the assay using monoclonal antibodies against rDer p 2 could be useful for the environmental studies and for the standardization of mite allergen extracts.
机译:屋尘螨过敏原已被很好地确立为敏化剂,对诱发过敏性疾病很重要。为了分析变应原的表位并开发定量变应原暴露的方法,生产了抗重组Der p 2(rDer p 2)(Dermatophagoides pteronyssinus的主要变应原之一)的单克隆抗体。产生的四种单克隆抗体是物种特异性的,并且不会与粉虱(D. farinae)粗提物发生交叉反应。发现其中两个单克隆抗体为IgG1,其他为IgM。为了分析表位,将编码126个氨基酸(aa)的Der p 2 cDNA分为三个片段,这些片段带有几个重叠的肽,A(aa残基1-49),B(44-93)和C片段(84- 126)。三种单克隆抗体显示出对重组B片段和全长rDer p 2的反应性,但一种单克隆抗体仅与全长rDer p 2反应。使用两种不同的单克隆抗体开发了用于定量Der的两点捕获ELISA p 2在室内灰尘中。 rDer p 2的灵敏度极限为4 ng / ml,翼龙蕨粗提物的灵敏度极限为8 µg / ml。结果表明,使用针对rDer p 2的单克隆抗体进行的测定可用于环境研究和螨过敏原提取物的标准化。

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