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通过比色PCR检测法直接检测外周血淋巴细胞中人类免疫缺陷病毒的前病毒gag片段,作为一种应用于不同高危人群的临床实验室工具。

Direct detection of proviral gag segment of human immunodeficiency virus in peripheral blood lymphocytes by colorimetric PCR assay as a clinical laboratory tool applied to different at-risk populations.

作者信息

Pane F, Buttò S, Gobbo M L, Franco M, Butteroni C, Pastore L, Maiorano G, Foggia M, Cataldo P T, Guarino A

机构信息

CEINGE-Biotecnologie Avanzate, Università di Napoli Federico II, Italy.

出版信息

J Clin Microbiol. 1995 Mar;33(3):641-7. doi: 10.1128/jcm.33.3.641-647.1995.

Abstract

We used a colorimetric polymerase chain reaction (PCR)-based assay in kit form to detect directly human immunodeficiency virus type 1 (HIV-1) proviral gag sequences in peripheral blood cells from 68 healthy blood donors, 51 subjects at risk for HIV infection, 122 patients with HIV-1 infection, 11 patients with indeterminate Western blot (immunoblot) results, 4 blood donors HIV-1 positive by enzyme immunoassay, and 13 children born to HIV-1-seropositive mothers. The results obtained in the blood donors and HIV-1-infected patients demonstrated the high degree of diagnostic specificity and sensitivity of the PCR method. HIV-1 infection was excluded in 10 of the 11 patients with indeterminate Western blot results and in all four enzyme immunoassay-positive blood donors. A diagnosis of HIV infection was ruled out by negative PCR results in 5 of 13 children from seropositive mothers, which excluded vertical transmission of the infection in these cases; these children were younger than 3 months and had positive serological results. Two at-risk patients with negative serological results had positive PCR results. All results were confirmed by conventional PCR. In conclusion, colorimetric PCR, which is commercially available in kit form, is an easy and reliable technique that can be used to detect proviral HIV-1 genomes in blood cells, and despite the limitations owing to HIV genome variability, it is useful in the clinical setting for the diagnosis of HIV infection in selected categories of patients.

摘要

我们使用了试剂盒形式的基于比色聚合酶链反应(PCR)的检测方法,直接检测68名健康献血者、51名有感染人类免疫缺陷病毒1型(HIV-1)风险的受试者、122名HIV-1感染患者、11名免疫印迹结果不确定的患者、4名酶免疫测定显示HIV-1阳性的献血者以及13名HIV-1血清反应阳性母亲所生儿童外周血细胞中的HIV-1前病毒gag序列。在献血者和HIV-1感染患者中获得的结果证明了PCR方法具有高度的诊断特异性和敏感性。11名免疫印迹结果不确定的患者中有10名以及所有4名酶免疫测定阳性的献血者被排除HIV-1感染。13名血清反应阳性母亲所生儿童中有5名PCR结果为阴性,从而排除了这些病例中的感染垂直传播;这些儿童年龄小于3个月且血清学结果为阳性,由此排除了HIV感染的诊断。2名血清学结果为阴性的有感染风险的患者PCR结果为阳性。所有结果均通过常规PCR得到证实。总之,试剂盒形式的比色PCR是一种简便可靠的技术,可用于检测血细胞中的HIV-1前病毒基因组,尽管由于HIV基因组变异性存在局限性,但它在临床环境中对于特定类型患者的HIV感染诊断很有用。

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HIV variability and perspectives for a vaccine.
Vaccine. 1993;11(5):542-4. doi: 10.1016/0264-410x(93)90227-o.
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