刚地弓形虫免疫球蛋白G含量测定的简化方法

H. Prince, Marianna Wilson
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引用次数: 34

摘要

建立了一种基于终点滴度的弓形虫免疫球蛋白G (IgG)亲和度酶联免疫吸附测定(ELISA)方法,该方法结合了基于光密度值的测定的准确性和相对易于性。与已发表的方法一样,新方法的亲和力指数(AI)基于尿素缓冲液洗涤的血清处理井与对照缓冲液洗涤的血清处理井中弓形虫特异性IgG反应性的差异;然而,与以往的分析不同,IgG的反应性是用标准曲线定量测量的。使用症状出现后5个月内收集的24份igg阳性和igm阳性血清(最近感染组)和25份igg阳性和igm阴性血清(过去感染组)对该检测进行评估。近期感染组血清AI值均为0.27。新近感染组的AI值与出现症状后的天数有显著相关性。使用市售let测试了16个血清子集(8个最近的和8个过去的)。终点滴定法检测弓形虫IgG亲和力ELISA;两项检测结果呈极显著相关(R2 = 0.9125)。此外,我们证实并扩展了其他研究者的发现,表明使用光密度值计算的AI值,而不是使用定量IgG值计算的AI值,根据所使用的血清稀释度而显着变化。这种新的测定方法应该有助于在参考实验室环境中准确测量弓形虫IgG的亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simplified Assay for Measuring Toxoplasma gondii Immunoglobulin G Avidity
ABSTRACT A Toxoplasma gondii immunoglobulin G (IgG) avidity enzyme-linked immunosorbent assay (ELISA) was developed that combines the accuracy of assays based on end point titers and the relative ease of assays based on optical density values. Like published procedures, the new assay's avidity index (AI) was based on differential T. gondii-specific IgG reactivity in serum-treated wells washed with urea buffer versus that in wells washed with control buffer; unlike previous assays, however, the IgG reactivity was measured quantitatively using a standard curve. The assay was evaluated using 24 IgG-positive and IgM-positive sera collected within 5 months of the onset of symptoms (recent-infection group) and 25 IgG-positive and IgM-negative sera (past-infection group). All sera in the recent-infection group exhibited AI values of <0.18, whereas all sera in the past-infection group exhibited AI values of >0.27. The AI values of the recent-infection group showed significant correlation with the number of days after the onset of symptoms. A subset of 16 sera (8 recent and 8 past) was tested using a commercially availableT. gondii IgG avidity ELISA based on end point titration; the results of the two assays showed highly significant correlation (R2 = 0.9125). In addition, we confirmed and extended the findings of other investigators, showing that AI values calculated using optical density values, but not AI values calculated using quantitative IgG values, varied significantly depending on the serum dilution used. This new assay should facilitate the accurate measurement of T. gondii IgG avidity in a reference laboratory setting.
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