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五个抗HIV-1 O亚型标本与六种不同的抗HIV筛查酶联免疫吸附测定(ELISA)和三种免疫印迹法的反应性。

Reactivity of five anti-HIV-1 subtype O specimens with six different anti-HIV screening ELISAs and three immunoblots.

作者信息

Gürtler L G, Zekeng L, Simon F, Eberle J, Tsague J M, Kaptue L, Brust S, Knapp S

机构信息

Max von Pettenkofer Institute, University of Munich, Germany.

出版信息

J Virol Methods. 1995 Feb;51(2-3):177-83. doi: 10.1016/0166-0934(94)00102-m.

Abstract

Five anti-subtype O specimens were tested by anti-HIV-1/2 screening and confirmatory assays. They can be divided into three specimens, reactive with all ELISAs, independent of the nature of the antigen (recombinant proteins or peptides) and test configuration (indirect ELISA or double antigen/sandwich ELISA). One specimen was not detected by one peptide based ELISA. One specimen was only recognized by two ELISAs and should be considered as a marker sample for the weakness of currently used ELISAs with anti-subtype O. Three different immunoblot assays available commercially detected two of the specimens with a major binding of gp160 and other viral bands, especially the integrase and reverse transcriptase. Another two specimens lacked reactivity with glycoproteins almost completely, but showed some staining with the enzymes of HIV, and would most probably be interpreted as indeterminate. The fifth specimen, which was also missed by most of the ELISAs, had very faint staining of the gp160 and a very weak staining of p24, and would most probably be interpreted as negative. Adaption of currently available tests to anti-subtype O is needed for the future reliability of anti-HIV diagnostic reagents.

摘要

对五个抗O亚型标本进行了抗HIV-1/2筛查和确证试验。它们可分为三个标本,与所有酶联免疫吸附测定(ELISA)均呈反应性,与抗原性质(重组蛋白或肽)和检测模式(间接ELISA或双抗原/夹心ELISA)无关。一个标本未被一种基于肽的ELISA检测到。一个标本仅被两种ELISA识别,应被视为当前使用的抗O亚型ELISA存在缺陷的标记样本。市售的三种不同免疫印迹试验检测到其中两个标本与gp160及其他病毒条带主要结合,尤其是整合酶和逆转录酶。另外两个标本几乎完全缺乏与糖蛋白的反应性,但对HIV的酶有一些染色,很可能被判定为不确定。第五个标本也被大多数ELISA漏检,gp160染色非常淡,p24染色非常弱,很可能被判定为阴性。为了抗HIV诊断试剂未来的可靠性,需要对现有检测方法进行针对抗O亚型的改进。

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