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

被引:24
作者
Bonard, D
Rouet, F
Toni, TA
Minga, A
Huet, C
Ekouévi, DK
Dabis, F
Salamon, R
Rouzioux, C
机构
[1] ANRS 1220 PRIMO CI, Programme PAC CI, Ctr Diagnost & Rech SIDA, Abidjan, Cote Ivoire
[2] Ctr Integre Rech Bioclin Abidjan, Abidjan, Cote Ivoire
[3] Univ Victor Segalen Bordeaux 2, Unite INSERM 593, Bordeaux, France
[4] CHU Necker, Virol Lab, F-75015 Paris, France
关键词
heat-dissociated p24 antigen; HIV-1 RNA load; sub-Saharan Africa;
D O I
10.1097/00126334-200311010-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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, Cote d'lvoire, 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 greater than or equal to5 log(10) 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.
引用
收藏
页码:267 / 273
页数:7
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