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在西非科特迪瓦,对主要感染HIV-1 CRF02_AG毒株的成年人使用热解离p24抗原的改进检测方法进行现场评估。

Field evaluation of an improved assay using a heat-dissociated p24 antigen for adults mainly infected with HIV-1 CRF02_AG strains in Côte d'Ivoire, West Africa.

作者信息

Bonard D, Rouet F, Toni T A, Minga A, Huet C, Ekouévi D K, Dabis F, Salamon R, Rouzioux C

机构信息

Centre de Diagnostic et de Recherches sur le SIDA, CHU de Treichville, BP V3 Abidjan, Côte d'Ivoire, West Africa.

出版信息

J Acquir Immune Defic Syndr. 2003 Nov 1;34(3):267-73. doi: 10.1097/00126334-200311010-00002.

Abstract

The aim of this study was to evaluate the heat-dissociated p24 antigen (HD p24 Ag) assay as an alternative low-cost tool for diagnosis of HIV-1 infection and quantitation of HIV-1 RNA levels in African adults mainly infected with HIV-1 CRF02_AG strains. One hundred seventeen plasma specimens were obtained from HIV-1-seropositive subjects enrolled in the ANRS 1220 PRIMO-CI cohort (Abidjan, Côte d'Ivoire, West Africa). Results of the HD p24 Ag assay were comparable with those of HIV-1 RNA levels quantified in the same antibody-positive plasma samples by the Amplicor HIV-1 Monitor assay (1.5 version; Roche Diagnostics, Indianapolis, IN): sensitivity, 95.7% versus 96.6%, respectively; specificity (evaluated with samples from 75 seronegative subjects), 94.7% versus 100%, respectively. HD p24 Ag and HIV-1 RNA assays were weakly correlated (Spearman coefficient correlation, r = 0.33; P < 0.001) except for HIV-1 RNA levels of >/=5 log10 copies/mL (r = 0.62; P < 0.001). Quantitation of HD p24 antigenemia in 76 plasma specimens from 14 patients treated with highly active antiretroviral therapy demonstrated weaker changes during treatment than those observed with the HIV-1 RNA assay. Follow-up of infected patients using both markers showed different results. The reliability of the HD p24 Ag assay is questionable for clinical and biologic management as a surrogate tool for measurement of HIV-1 RNA levels in Africa.

摘要

本研究的目的是评估热解离p24抗原(HD p24 Ag)检测法,作为一种替代的低成本工具,用于诊断非洲主要感染HIV-1 CRF02_AG毒株的成年人的HIV-1感染及定量HIV-1 RNA水平。从参加ANRS 1220 PRIMO-CI队列研究(西非科特迪瓦阿比让)的HIV-1血清阳性受试者中获取了117份血浆标本。HD p24 Ag检测结果与通过Amplicor HIV-1 Monitor检测法(1.5版;罗氏诊断公司,印第安纳波利斯,印第安纳州)在相同抗体阳性血浆样本中定量的HIV-1 RNA水平的结果相当:敏感性分别为95.7%和96.6%;特异性(用来自75名血清阴性受试者的样本评估)分别为94.7%和100%。HD p24 Ag检测和HIV-1 RNA检测的相关性较弱(Spearman系数相关性,r = 0.33;P < 0.001),但HIV-1 RNA水平≥5 log10拷贝/mL时除外(r = 0.62;P < 0.001)。对14例接受高效抗逆转录病毒治疗的患者的76份血浆标本中的HD p24抗原血症进行定量分析,结果显示治疗期间的变化比HIV-1 RNA检测所观察到的变化小。使用这两种标志物对感染患者进行随访显示出不同的结果。在非洲,作为测量HIV-1 RNA水平的替代工具,HD p24 Ag检测法在临床和生物学管理方面的可靠性存在疑问。

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