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首页> 外文期刊>Journal of Clinical Microbiology >Quantification of immunoglobulin on electrophoretic immunoblot strips as a tool for human immunodeficiency virus serodiagnosis.
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Quantification of immunoglobulin on electrophoretic immunoblot strips as a tool for human immunodeficiency virus serodiagnosis.

机译:电泳免疫印迹试纸上免疫球蛋白的定量分析作为人类免疫缺陷病毒血清诊断的工具。

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Electrophoretic immunoblotting (EIB [Western blotting]), the main method for verification of human immunodeficiency virus (HIV) seropositivity, needs thorough characterization and standardization. We explored the possibilities of quantifying immunoglobulin G (IgG) bound to EIB strips both by densitometry of the peroxidase-stained bands and by measurement of radioactivity with labeled anti-HIV IgG. The radioactivity method is inherently more exact but was more cumbersome. However, despite saturation phenomena at high IgG densities, the densitometric method was more convenient and yielded reproducible estimates of the amount of bound IgG. We found it useful primarily for documentation of changes in the relative abundance of antibodies to different HIV proteins from individual patients over time. To explore the potential usefulness of the method, we studied a small set of HIV-seropositive persons. The average p24/gp41 color yield ratios and standard deviations in 3 persons with recent seroconversion, 15 healthy subjects, and 6 diseased HIV-seropositive persons were 6.6 +/- 0.9, 2.3 +/- 1.9, and 1.3 +/- 0.5, respectively. These data are in accord with previous qualitative or semiquantitative observations but are too limited for any conclusions regarding the use of quantitative EIB for prognostic use with individual patients. Quantitative EIB is a valuable tool for comparative methodological studies and for research on the protective role of anti-HIV antibodies in acquired immunodeficiency syndrome pathogenesis. Its possible use in prognostication for individual patients must be evaluated in long-term studies.
机译:电泳免疫印迹(EIB [Western blotting])是验证人类免疫缺陷病毒(HIV)血清阳性的主要方法,需要进行全面的表征和标准化。我们探索了通过过氧化物酶染色的条带的光密度测定和通过标记的抗HIV IgG的放射性测量来定量结合到EIB条的免疫球蛋白G(IgG)的可能性。放射性方法本来就更精确,但是比较麻烦。但是,尽管在高IgG密度下出现饱和现象,光密度测定法还是更方便的方法,并且可以重现结合IgG量的估计值。我们发现它主要用于记录随着时间​​推移来自各个患者的针对不同HIV蛋白的抗体相对丰度的变化。为了探索该方法的潜在用途,我们研究了一小批艾滋病毒血清阳性的人。 3名近期发生血清转化的人,15名健康受试者和6名艾滋病毒血清阳性的患者的平均p24 / gp41颜色产生率和标准差分别为6.6 +/- 0.9、2.3 +/- 1.9和1.3 +/- 0.5 。这些数据与先前的定性或半定量观察结果一致,但对于将定量EIB用于个体患者的预后使用的任何结论都太有限了。定量EIB是进行比较方法学研究和抗HIV抗体在获得性免疫缺陷综合症发病机制中的保护作用研究的宝贵工具。必须在长期研究中评估其可能用于个别患者的预后。

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