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[不同人群组中DNA-HIV检测的评估]

[Evaluation of DNA-HIV detection in various population groups].

作者信息

Quirós E, García F, Cabezas T, González I, Bernal M C, Maroto M C, Piedrola G

机构信息

Departamento de Microbiología (Facultad de Medicina), Universidad de Granada.

出版信息

Enferm Infecc Microbiol Clin. 1993 May;11(5):241-3.

PMID:8324019
Abstract

BACKGROUND

To evaluate the diagnostic use of Polymerase Chain Reaction (PCR) for the detection of HIV-DNA.

METHODS

We have investigated HIV-DNA in peripheral blood mononuclear cells of 150 individuals: 50 seronegative without recognized factors to acquire HIV infection, 50 seronegative that showed risk habits and 50 seropositive. For amplification we have used primers SK38/SK39 which amplify a conserved region of 114 bp from HIV's gag gen. The detection of the amplificate was performed using solution hybridization with 32P-labelled SK 19, 6% polyacrylamide gel electrophoresis and autoradiography.

RESULTS

We have detected HIV-DNA at every seropositive patient (100%), 6 samples from seronegative individuals that showed risk habits and 1 sample from non-risk seronegative individuals.

CONCLUSIONS

Polymerase chain reaction represents a diagnostic tool at HIV infection, specially for those patients where seroconversion can not be demonstrated by conventional methods.

摘要

背景

评估聚合酶链反应(PCR)用于检测HIV-DNA的诊断价值。

方法

我们检测了150名个体外周血单个核细胞中的HIV-DNA,其中50名血清学阴性且无已知感染HIV的危险因素,50名血清学阴性但有高危行为,50名血清学阳性。我们使用引物SK38/SK39进行扩增,该引物可扩增HIV gag基因中一段114 bp的保守区域。扩增产物的检测采用与32P标记的SK 19进行溶液杂交、6%聚丙烯酰胺凝胶电泳和放射自显影。

结果

我们在所有血清学阳性患者(100%)中检测到了HIV-DNA,在6名有高危行为的血清学阴性个体和1名无高危行为的血清学阴性个体中也检测到了HIV-DNA。

结论

聚合酶链反应是HIV感染的一种诊断工具,尤其适用于那些无法通过传统方法证实血清转化的患者。

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