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Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration

BACKGROUND: Plasma HIV-1 RNA monitoring is one of the standard tests for the management of HIV-1 infection. While HIV-1 RNA can be quantified using several commercial tests, no test has been commercialized for HIV-2 RNA quantification. We studied the relationship between plasma HIV-2 viral load (VL)...

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Autores principales: Ekouévi, Didier K., Avettand-Fènoël, Véronique, Tchounga, Boris K., Coffie, Patrick A., Sawadogo, Adrien, Minta, Daouda, Minga, Albert, Eholie, Serge P., Plantier, Jean-Christophe, Damond, Florence, Dabis, François, Rouzioux, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482391/
https://www.ncbi.nlm.nih.gov/pubmed/26111242
http://dx.doi.org/10.1371/journal.pone.0129886
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author Ekouévi, Didier K.
Avettand-Fènoël, Véronique
Tchounga, Boris K.
Coffie, Patrick A.
Sawadogo, Adrien
Minta, Daouda
Minga, Albert
Eholie, Serge P.
Plantier, Jean-Christophe
Damond, Florence
Dabis, François
Rouzioux, Christine
author_facet Ekouévi, Didier K.
Avettand-Fènoël, Véronique
Tchounga, Boris K.
Coffie, Patrick A.
Sawadogo, Adrien
Minta, Daouda
Minga, Albert
Eholie, Serge P.
Plantier, Jean-Christophe
Damond, Florence
Dabis, François
Rouzioux, Christine
author_sort Ekouévi, Didier K.
collection PubMed
description BACKGROUND: Plasma HIV-1 RNA monitoring is one of the standard tests for the management of HIV-1 infection. While HIV-1 RNA can be quantified using several commercial tests, no test has been commercialized for HIV-2 RNA quantification. We studied the relationship between plasma HIV-2 viral load (VL) and CD4 count in West African patients who were either receiving antiretroviral therapy (ART) or treatment-naïve. METHOD: A cross sectional survey was conducted among HIV-2-infected individuals followed in three countries in West Africa from March to December 2012. All HIV-2 infected-patients who attended one of the participating clinics were proposed a plasma HIV-2 viral load measurement. HIV-2 RNA was quantified using the new ultrasensitive in-house real-time PCR assay with a detection threshold of 10 copies/ mL (cps/mL). RESULTS: A total of 351 HIV-2-infected individuals participated in this study, of whom 131 (37.3%) were treatment naïve and 220 (62.7%) had initiated ART. Among treatment-naïve patients, 60 (46.5%) had undetectable plasma HIV-2 viral load (<10 cps/mL), it was detectable between 10-100 cps/mL in 35.8%, between 100-1000 cps/mL in 11.7% and >1000 cps/mL in 6.0% of the patients. Most of the treatment-naïve patients (70.2%) had CD4-T cell count ≥500 cells/mm(3) and 43 (46.7%) of these patients had a detectable VL (≥10 cps/mL). Among the 220 patients receiving ART, the median CD4-T cell count rose from 231 to 393 cells/mm(3) (IQR [259-561]) after a median follow-up duration of 38 months and 145 (66.0%) patients had CD4-T cell count ≤ 500 cells/mm(3) with a median viral load of 10 cps/mL (IQR [10-33]). Seventy five (34.0%) patients had CD4-T cell count ≥ 500 cells/mm(3), among them 14 (18.7%) had a VL between 10-100 cps/mL and 2 (2.6%) had VL >100 cps/mL. CONCLUSION: This study suggests that the combination of CD4-T cell count and ultrasensitive HIV-2 viral load quantification with a threshold of 10 cps/mL, could improve ART initiation among treatment naïve HIV-2-infected patients and the monitoring of ART response among patients receiving treatment.
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spelling pubmed-44823912015-07-01 Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration Ekouévi, Didier K. Avettand-Fènoël, Véronique Tchounga, Boris K. Coffie, Patrick A. Sawadogo, Adrien Minta, Daouda Minga, Albert Eholie, Serge P. Plantier, Jean-Christophe Damond, Florence Dabis, François Rouzioux, Christine PLoS One Research Article BACKGROUND: Plasma HIV-1 RNA monitoring is one of the standard tests for the management of HIV-1 infection. While HIV-1 RNA can be quantified using several commercial tests, no test has been commercialized for HIV-2 RNA quantification. We studied the relationship between plasma HIV-2 viral load (VL) and CD4 count in West African patients who were either receiving antiretroviral therapy (ART) or treatment-naïve. METHOD: A cross sectional survey was conducted among HIV-2-infected individuals followed in three countries in West Africa from March to December 2012. All HIV-2 infected-patients who attended one of the participating clinics were proposed a plasma HIV-2 viral load measurement. HIV-2 RNA was quantified using the new ultrasensitive in-house real-time PCR assay with a detection threshold of 10 copies/ mL (cps/mL). RESULTS: A total of 351 HIV-2-infected individuals participated in this study, of whom 131 (37.3%) were treatment naïve and 220 (62.7%) had initiated ART. Among treatment-naïve patients, 60 (46.5%) had undetectable plasma HIV-2 viral load (<10 cps/mL), it was detectable between 10-100 cps/mL in 35.8%, between 100-1000 cps/mL in 11.7% and >1000 cps/mL in 6.0% of the patients. Most of the treatment-naïve patients (70.2%) had CD4-T cell count ≥500 cells/mm(3) and 43 (46.7%) of these patients had a detectable VL (≥10 cps/mL). Among the 220 patients receiving ART, the median CD4-T cell count rose from 231 to 393 cells/mm(3) (IQR [259-561]) after a median follow-up duration of 38 months and 145 (66.0%) patients had CD4-T cell count ≤ 500 cells/mm(3) with a median viral load of 10 cps/mL (IQR [10-33]). Seventy five (34.0%) patients had CD4-T cell count ≥ 500 cells/mm(3), among them 14 (18.7%) had a VL between 10-100 cps/mL and 2 (2.6%) had VL >100 cps/mL. CONCLUSION: This study suggests that the combination of CD4-T cell count and ultrasensitive HIV-2 viral load quantification with a threshold of 10 cps/mL, could improve ART initiation among treatment naïve HIV-2-infected patients and the monitoring of ART response among patients receiving treatment. Public Library of Science 2015-06-25 /pmc/articles/PMC4482391/ /pubmed/26111242 http://dx.doi.org/10.1371/journal.pone.0129886 Text en © 2015 Ekouévi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ekouévi, Didier K.
Avettand-Fènoël, Véronique
Tchounga, Boris K.
Coffie, Patrick A.
Sawadogo, Adrien
Minta, Daouda
Minga, Albert
Eholie, Serge P.
Plantier, Jean-Christophe
Damond, Florence
Dabis, François
Rouzioux, Christine
Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title_full Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title_fullStr Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title_full_unstemmed Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title_short Plasma HIV-2 RNA According to CD4 Count Strata among HIV-2-Infected Adults in the IeDEA West Africa Collaboration
title_sort plasma hiv-2 rna according to cd4 count strata among hiv-2-infected adults in the iedea west africa collaboration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482391/
https://www.ncbi.nlm.nih.gov/pubmed/26111242
http://dx.doi.org/10.1371/journal.pone.0129886
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