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Journal of Clinical Microbiology, September 2004, p. 4147-4153, Vol. 42, No. 9
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.9.4147-4153.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Field Evaluation of a Rapid Human Immunodeficiency Virus (HIV) Serial Serologic Testing Algorithm for Diagnosis and Differentiation of HIV Type 1 (HIV-1), HIV-2, and Dual HIV-1-HIV-2 Infections in West African Pregnant Women

François Rouet,^1,2* Didier K. Ekouevi,^2,3 André Inwoley,^1,2 Marie-Laure Chaix,⁴ Marianne Burgard,⁴ Laurence Bequet,² Ida Viho,² Valériane Leroy,^2,3 François Simon,⁵ François Dabis,^2,3 and Christine Rouzioux⁴

Centre de Diagnostic et de Recherches sur le SIDA, CHU de Treichville,¹ Programme ANRS 1201/1202 Ditrame Plus, PAC-CI, Abidjan, Côte d'Ivoire,² Unité INSERM 593, Université Victor Segalen, Bordeaux,³ Laboratoire de Virologie, CHU Necker, Paris, France,⁴ Institut Pasteur, Dakar, Sénégal⁵

Received 31 October 2003/ Returned for modification 21 February 2004/ Accepted 15 May 2004

We evaluated a two-rapid-test serial algorithm using the Determine and Genie II rapid assays, performed on-site in four peripheral laboratories during the French Agence Nationale de Recherches sur le SIDA (ANRS) 1201/1202 Ditrame Plus cohort developed for prevention of mother-to-child transmission of human immunodeficiency virus (HIV) infection in Côte d'Ivoire. A total of 1,039 specimens were retested by two commercial enzyme-linked immunosorbent assays (ELISAs). The following specimens were tested: 315 specimens found on-site to be infected with HIV type 1 (HIV-1), 8 specimens found on-site to be infected with HIV-2, 71 specimens found on-site to be infected with both HIV-1 and HIV-2, 40 specimens found on-site to have indeterminate results for HIV infection, and 605 specimens taken during a quality assurance program. For HIV discrimination, 99 positive serum samples (20 with HIV-1, 8 with HIV-2, and 71 with HIV-1 and HIV-2 on the basis of our rapid test algorithm) were retested by the Peptilav test, Western blot (WB) assays, and homemade monospecific ELISAs. Real-time DNA PCRs for the detection of HIV-1 and HIV-2 were performed with peripheral blood mononuclear cells from 35 women diagnosed on-site with HIV-1 and HIV-2 infections. Compared to the results of the ELISAs, the sensitivities of the Determine and Genie II assays were 100% (95% lower limit [95% LL], 99.1%) and 99.5% (95% confidence interval [95% CI], 98.2 to 99.9%), respectively. The specificities were 98.4% (95% CI, 96.9 to 99.3%) and 100% (95% LL, 99.3%), respectively. All serological assays gave concordant results for infections with single types. By contrast, for samples found to be infected with dual HIV types by the Genie II assay, dual reactivity was detected for only 37 samples (52.1%) by WB assays, 34 samples (47.9%) by the Peptilav assay, and 23 samples (32.4%) by the monospecific ELISAs. For specimens with dual reactivity by the Genie II assay, the rates of concordance between the real-time PCR assays and the serological assays were 25.7% for the Genie II assay, 82.9% for the Peptilav assay, 74.3% for WB assays, and 80% for the homemade ELISAs. Our algorithm provided high degrees of sensitivity and specificity comparable to those of ELISAs. Even if they are rare, women identified by the Genie II assay as being infected with HIV-1 and HIV-2 mostly appeared to be infected only with HIV-2.

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* Corresponding author. Mailing address: CeDReS, Programme PAC-CI, CHU de Treichville, BP V3 Abidjan, Côte d'Ivoire. Phone: 225 21 25 77 53. Fax: 225 21 24 92 06. E-mail: rouet{at}aviso.ci.

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Journal of Clinical Microbiology, September 2004, p. 4147-4153, Vol. 42, No. 9
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.9.4147-4153.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

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