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Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission

BACKGROUND: Current WHO guidelines recommend antiretroviral therapy (ART) initiation at CD4 counts ≤350 cells/µL. Increasing this threshold has been proposed, with a primary goal of reducing HIV-1 infectiousness. Because the quantity of HIV-1 in plasma is the primary predictor of HIV-1 transmission,...

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Autores principales: Murnane, Pamela M., Hughes, James P., Celum, Connie, Lingappa, Jairam R., Mugo, Nelly, Farquhar, Carey, Kiarie, James, Wald, Anna, Baeten, Jared M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511400/
https://www.ncbi.nlm.nih.gov/pubmed/23250272
http://dx.doi.org/10.1371/journal.pone.0051192
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author Murnane, Pamela M.
Hughes, James P.
Celum, Connie
Lingappa, Jairam R.
Mugo, Nelly
Farquhar, Carey
Kiarie, James
Wald, Anna
Baeten, Jared M.
author_facet Murnane, Pamela M.
Hughes, James P.
Celum, Connie
Lingappa, Jairam R.
Mugo, Nelly
Farquhar, Carey
Kiarie, James
Wald, Anna
Baeten, Jared M.
author_sort Murnane, Pamela M.
collection PubMed
description BACKGROUND: Current WHO guidelines recommend antiretroviral therapy (ART) initiation at CD4 counts ≤350 cells/µL. Increasing this threshold has been proposed, with a primary goal of reducing HIV-1 infectiousness. Because the quantity of HIV-1 in plasma is the primary predictor of HIV-1 transmission, consideration of plasma viral load in ART initiation guidelines is warranted. METHODS: Using per-sex-act infectivity estimates and cross-sectional sexual behavior data from 2,484 HIV-1 infected persons with CD4 counts >350 enrolled in a study of African heterosexual HIV-1 serodiscordant couples, we calculated the number of transmissions expected and the number potentially averted under selected scenarios for ART initiation: i) CD4 count <500 cells/µL, ii) viral load ≥10,000 or ≥50,000 copies/mL and iii) universal treatment. For each scenario, we estimated the proportion of expected infections that could be averted, the proportion of infected persons initiating treatment, and the ratio of these proportions. RESULTS: Initiating treatment at viral load ≥50,000 copies/mL would require treating 19.8% of infected persons with CD4 counts >350 while averting 40.5% of expected transmissions (ratio 2.0); treating at viral load ≥10,0000 copies/mL had a ratio of 1.5. In contrast, initiation at CD4 count <500 would require treating 41.8%, while averting 48.4% (ratio 1.1). CONCLUSION: Inclusion of viral load in ART initiation guidelines could permit targeting ART resources to HIV-1 infected persons who have a higher risk of transmitting HIV-1. Further work is needed to estimate costs and feasibility.
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spelling pubmed-35114002012-12-05 Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission Murnane, Pamela M. Hughes, James P. Celum, Connie Lingappa, Jairam R. Mugo, Nelly Farquhar, Carey Kiarie, James Wald, Anna Baeten, Jared M. PLoS One Research Article BACKGROUND: Current WHO guidelines recommend antiretroviral therapy (ART) initiation at CD4 counts ≤350 cells/µL. Increasing this threshold has been proposed, with a primary goal of reducing HIV-1 infectiousness. Because the quantity of HIV-1 in plasma is the primary predictor of HIV-1 transmission, consideration of plasma viral load in ART initiation guidelines is warranted. METHODS: Using per-sex-act infectivity estimates and cross-sectional sexual behavior data from 2,484 HIV-1 infected persons with CD4 counts >350 enrolled in a study of African heterosexual HIV-1 serodiscordant couples, we calculated the number of transmissions expected and the number potentially averted under selected scenarios for ART initiation: i) CD4 count <500 cells/µL, ii) viral load ≥10,000 or ≥50,000 copies/mL and iii) universal treatment. For each scenario, we estimated the proportion of expected infections that could be averted, the proportion of infected persons initiating treatment, and the ratio of these proportions. RESULTS: Initiating treatment at viral load ≥50,000 copies/mL would require treating 19.8% of infected persons with CD4 counts >350 while averting 40.5% of expected transmissions (ratio 2.0); treating at viral load ≥10,0000 copies/mL had a ratio of 1.5. In contrast, initiation at CD4 count <500 would require treating 41.8%, while averting 48.4% (ratio 1.1). CONCLUSION: Inclusion of viral load in ART initiation guidelines could permit targeting ART resources to HIV-1 infected persons who have a higher risk of transmitting HIV-1. Further work is needed to estimate costs and feasibility. Public Library of Science 2012-11-30 /pmc/articles/PMC3511400/ /pubmed/23250272 http://dx.doi.org/10.1371/journal.pone.0051192 Text en © 2012 Murnane 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
Murnane, Pamela M.
Hughes, James P.
Celum, Connie
Lingappa, Jairam R.
Mugo, Nelly
Farquhar, Carey
Kiarie, James
Wald, Anna
Baeten, Jared M.
Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title_full Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title_fullStr Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title_full_unstemmed Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title_short Using Plasma Viral Load to Guide Antiretroviral Therapy Initiation to Prevent HIV-1 Transmission
title_sort using plasma viral load to guide antiretroviral therapy initiation to prevent hiv-1 transmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511400/
https://www.ncbi.nlm.nih.gov/pubmed/23250272
http://dx.doi.org/10.1371/journal.pone.0051192
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