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HIV-1 persistent viremia is frequently followed by episodes of low-level viremia

After the start of antiretroviral therapy (ART), plasma HIV-RNA levels should fall below the limit of detection (LOD) within 24 weeks. Hence, the prolonged decline of HIV-RNA after ART initiation is defined as persistent viremia (PV). In this retrospective study, we analyzed factors associated with...

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Autores principales: Widera, Marek, Dirks, Miriam, Bleekmann, Barbara, Jablonka, Robert, Däumer, Martin, Walter, Hauke, Ehret, Robert, Verheyen, Jens, Esser, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409919/
https://www.ncbi.nlm.nih.gov/pubmed/28220254
http://dx.doi.org/10.1007/s00430-017-0494-1
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author Widera, Marek
Dirks, Miriam
Bleekmann, Barbara
Jablonka, Robert
Däumer, Martin
Walter, Hauke
Ehret, Robert
Verheyen, Jens
Esser, Stefan
author_facet Widera, Marek
Dirks, Miriam
Bleekmann, Barbara
Jablonka, Robert
Däumer, Martin
Walter, Hauke
Ehret, Robert
Verheyen, Jens
Esser, Stefan
author_sort Widera, Marek
collection PubMed
description After the start of antiretroviral therapy (ART), plasma HIV-RNA levels should fall below the limit of detection (LOD) within 24 weeks. Hence, the prolonged decline of HIV-RNA after ART initiation is defined as persistent viremia (PV). In this retrospective study, we analyzed factors associated with PV. Next-generation sequencing of viral RNA/DNA was performed to study viral evolution and the emergence of drug-resistance mutations in HIV-infected patients with PV (n = 20). In addition, HIV-DNA species, immunological parameters, and clinical data of the patients were analyzed. We found that the possible causes for PV were divers, and both virologic and host parameters of this particular cohort were heterogeneous. We identified viruses with therapy-associated DRMs in six patients (30%); two of these were detected as minority variants. Five patients had sub-optimal drug levels (25%) and the baseline plasma viral loads were relatively high. Strikingly, we observed that >40% of the PV patients finally reaching HIV levels below the LOD later on showed up with episodes of low-level viremia (LLV). However, the amount of PBMC derived HIV-DNA species was not correlated with the likelihood of LLV after PV. According to our data, we conclude that drug-resistant viruses, sub-optimal drug level, and high baseline viral loads might be probable reasons for the prolonged RNA decline only in a sub-set of patients. In the absence of emerging DRMs and/or compliance issues, the clinical implications of PV remain unclear; however, PV appears to be a risk factor for episodes of LLV.
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spelling pubmed-54099192017-05-15 HIV-1 persistent viremia is frequently followed by episodes of low-level viremia Widera, Marek Dirks, Miriam Bleekmann, Barbara Jablonka, Robert Däumer, Martin Walter, Hauke Ehret, Robert Verheyen, Jens Esser, Stefan Med Microbiol Immunol Original Investigation After the start of antiretroviral therapy (ART), plasma HIV-RNA levels should fall below the limit of detection (LOD) within 24 weeks. Hence, the prolonged decline of HIV-RNA after ART initiation is defined as persistent viremia (PV). In this retrospective study, we analyzed factors associated with PV. Next-generation sequencing of viral RNA/DNA was performed to study viral evolution and the emergence of drug-resistance mutations in HIV-infected patients with PV (n = 20). In addition, HIV-DNA species, immunological parameters, and clinical data of the patients were analyzed. We found that the possible causes for PV were divers, and both virologic and host parameters of this particular cohort were heterogeneous. We identified viruses with therapy-associated DRMs in six patients (30%); two of these were detected as minority variants. Five patients had sub-optimal drug levels (25%) and the baseline plasma viral loads were relatively high. Strikingly, we observed that >40% of the PV patients finally reaching HIV levels below the LOD later on showed up with episodes of low-level viremia (LLV). However, the amount of PBMC derived HIV-DNA species was not correlated with the likelihood of LLV after PV. According to our data, we conclude that drug-resistant viruses, sub-optimal drug level, and high baseline viral loads might be probable reasons for the prolonged RNA decline only in a sub-set of patients. In the absence of emerging DRMs and/or compliance issues, the clinical implications of PV remain unclear; however, PV appears to be a risk factor for episodes of LLV. Springer Berlin Heidelberg 2017-02-20 2017 /pmc/articles/PMC5409919/ /pubmed/28220254 http://dx.doi.org/10.1007/s00430-017-0494-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Investigation
Widera, Marek
Dirks, Miriam
Bleekmann, Barbara
Jablonka, Robert
Däumer, Martin
Walter, Hauke
Ehret, Robert
Verheyen, Jens
Esser, Stefan
HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title_full HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title_fullStr HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title_full_unstemmed HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title_short HIV-1 persistent viremia is frequently followed by episodes of low-level viremia
title_sort hiv-1 persistent viremia is frequently followed by episodes of low-level viremia
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409919/
https://www.ncbi.nlm.nih.gov/pubmed/28220254
http://dx.doi.org/10.1007/s00430-017-0494-1
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