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桥接 ELISA 法在人血清中检测抗促红细胞生成素结合抗体和中和抗体的应用及基于细胞的生物测定法。

Application of a bridging ELISA for detection of anti-erythropoietin binding antibodies and a cell-based bioassay for neutralizing antibodies in human sera.

机构信息

Department of Internal Medicine, Ilsan Hospital, National Health Insurance Cooperation, Goyang-shi, Republic of Korea.

出版信息

J Pharm Biomed Anal. 2010 Jun 5;52(2):289-93. doi: 10.1016/j.jpba.2010.01.022. Epub 2010 Jan 18.

Abstract

Although erythropoietin (EPO)-related pure red-cell aplasia (PRCA) is a rare disorder, attention still needs to be paid because underline mechanism of EPO immunogenicity is various and controversial. Among several assay systems for screening of anti-EPO binding antibodies (Abs), we adopted and setup the bridging ELISA using streptavidin-coated plate. To test their neutralizing activities, cell-based neutralizing (NT) bioassay was setup. When we analyzed serum samples by using these two assays, we found two positive results in the two samples. In the sample 1, 411.9 ng/ml of anti-EPO Abs were found and neutralizing activity of 36.2% at 1:5 serum dilution was detected. In the sample 2, 40.5 ng/ml of anti-EPO Abs were found and neutralizing activity of 96.7% was detected. Our results indicate that the higher anti-EPO antibody (Ab) level in a serum does not always lead to the stronger neutralizing activity. This report gives crucial consideration to the needs of establishing clear criteria to link various assay parameters with the onset of PRCA and its progression.

摘要

虽然促红细胞生成素(EPO)相关纯红细胞再生障碍性贫血(PRCA)是一种罕见的疾病,但仍需要引起关注,因为 EPO 免疫原性的潜在机制是多种多样且存在争议的。在几种用于筛选抗 EPO 结合抗体(Abs)的检测系统中,我们采用了并建立了使用链霉亲和素包被板的桥接 ELISA。为了测试它们的中和活性,建立了基于细胞的中和(NT)生物测定法。当我们使用这两种检测方法分析血清样本时,在两个样本中发现了两个阳性结果。在样本 1 中,发现了 411.9ng/ml 的抗 EPO Abs,在 1:5 血清稀释度下检测到 36.2%的中和活性。在样本 2 中,发现了 40.5ng/ml 的抗 EPO Abs,检测到 96.7%的中和活性。我们的结果表明,血清中较高的抗 EPO 抗体(Ab)水平并不总是导致更强的中和活性。本报告对需要建立明确的标准以将各种检测参数与 PRCA 的发病及其进展联系起来给予了重要考虑。

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