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基于肽、重组蛋白和病毒裂解物的酶联免疫吸附试验检测HIV-1抗体的比较性能。

Comparative performance of peptide-, recombinant protein-, and viral lysate-based enzyme immunosorbent assays for the detection of HIV-1 antibodies.

作者信息

Griffith B P, Chacko T M

机构信息

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut.

出版信息

Diagn Microbiol Infect Dis. 1993 May-Jun;16(4):331-5. doi: 10.1016/0732-8893(93)90085-l.

Abstract

The performance of peptide-, recombinant protein-, and whole virus lysate-based enzyme immunosorbent assays (EIAs) for the detection of antibodies to the human immunodeficiency virus type 1 (HIV-1) was compared on a panel of 245 routine samples, a panel of low-positive samples, four seroconversion panels, and serial dilutions of five known positive samples. Of the 245 routine samples, 83 were confirmed to be HIV-1 antibody positive by Western blot and were reactive in the three EIAs used. Agreement between the three EIA tests was also 100% for all 162 negative samples. Although there was no significant difference in the performance of the three types of assays in seroconversion panels, the whole virus and recombinant protein-based EIAs detected 15 of 15 samples in the low-positive panel whereas only 10 of 15 samples were reactive when the peptide-based EIA was used. In addition, evaluation of diluted positive samples suggested that the virus lysate-based EIA was more sensitive than the peptide- and recombinant-based EIAs. These results show that although the three types of assays performed well on routine serum panels, differences in sensitivities were demonstrated when performance panels were evaluated. The data suggest that seroconversion and low-positive performance panels should be included in evaluations of new generations of EIAs for HIV-1 antibodies.

摘要

在一组245份常规样本、一组低阳性样本、四个血清转化样本组以及五个已知阳性样本的系列稀释样本上,比较了基于肽、重组蛋白和全病毒裂解物的酶联免疫吸附测定(EIA)检测1型人类免疫缺陷病毒(HIV-1)抗体的性能。在245份常规样本中,83份经蛋白质印迹法确认为HIV-1抗体阳性,并且在所使用的三种EIA检测中呈反应性。对于所有162份阴性样本,三种EIA检测之间的一致性也为100%。尽管在血清转化样本组中三种检测类型的性能没有显著差异,但基于全病毒和重组蛋白的EIA在低阳性样本组中检测出15份样本中的15份,而使用基于肽的EIA时,15份样本中只有10份呈反应性。此外,对稀释阳性样本的评估表明,基于病毒裂解物的EIA比基于肽和重组蛋白的EIA更敏感。这些结果表明,尽管三种检测类型在常规血清样本组中表现良好,但在评估性能样本组时显示出敏感性差异。数据表明,血清转化和低阳性性能样本组应纳入新一代HIV-1抗体EIA的评估中。

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