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用于测量IgE抗体的夹心酶联免疫吸附测定法的灵敏度和特异性提高。

Increased sensitivity and specificity of a sandwich ELISA for measurement of IgE antibodies.

作者信息

Kemeny D M, Urbanek R, Samuel D, Richards D

出版信息

J Immunol Methods. 1985 Apr 22;78(2):217-26. doi: 10.1016/0022-1759(85)90079-1.

Abstract

We have developed a sandwich enzyme-linked immunosorbent assay (ELISA) for measurement of IgE antibodies to the bee venom allergens phospholipase A2 (PLA2) and hyaluronidase (HYAL). The assay is 10-20 times more sensitive than conventional indirect ELISA or radioallergosorbent test (RAST). Furthermore, by using affinity purified rabbit antibodies to these allergens, the specificity of the test was increased compared to RAST. The use of antibodies to link the antigen to the solid phase removes the dependence on the individual protein's ability to bind to the microtitre plate. The increased sensitivity of the sandwich assay seems to be due to better presentation and retention of antigen on the solid phase.

摘要

我们开发了一种夹心酶联免疫吸附测定法(ELISA),用于测量针对蜂毒过敏原磷脂酶A2(PLA2)和透明质酸酶(HYAL)的IgE抗体。该测定法的灵敏度比传统间接ELISA或放射变应原吸附试验(RAST)高10至20倍。此外,通过使用针对这些过敏原的亲和纯化兔抗体,与RAST相比,该测试的特异性有所提高。使用抗体将抗原连接到固相上消除了对单个蛋白质与微量滴定板结合能力的依赖。夹心测定法灵敏度的提高似乎是由于抗原在固相上的更好呈现和保留。

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