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Predictors of SIV recrudescence following antiretroviral treatment interruption
There is currently a need for proxy measures of the HIV rebound competent reservoir (RCR) that can predict viral rebound after combined antiretroviral treatment (cART) interruption. In this study, macaques infected with a barcoded SIVmac239 virus received cART beginning between 4- and 27 days post-i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917497/ https://www.ncbi.nlm.nih.gov/pubmed/31650954 http://dx.doi.org/10.7554/eLife.49022 |
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author | Pinkevych, Mykola Fennessey, Christine M Cromer, Deborah Reid, Carolyn Trubey, Charles M Lifson, Jeffrey D Keele, Brandon F Davenport, Miles P |
author_facet | Pinkevych, Mykola Fennessey, Christine M Cromer, Deborah Reid, Carolyn Trubey, Charles M Lifson, Jeffrey D Keele, Brandon F Davenport, Miles P |
author_sort | Pinkevych, Mykola |
collection | PubMed |
description | There is currently a need for proxy measures of the HIV rebound competent reservoir (RCR) that can predict viral rebound after combined antiretroviral treatment (cART) interruption. In this study, macaques infected with a barcoded SIVmac239 virus received cART beginning between 4- and 27 days post-infection, leading to the establishment of different levels of viral dissemination and persistence. Later treatment initiation led to higher SIV DNA levels maintained during treatment, which was significantly associated with an increased frequency of SIV reactivation and production of progeny capable of causing rebound viremia following treatment interruption. However, a 100-fold increase in SIV DNA in PBMCs was associated with only a 2-fold increase in the frequency of reactivation. These data suggest that the RCR can be established soon after infection, and that a large fraction of persistent viral DNA that accumulates after this time makes relatively little contribution to viral rebound. |
format | Online Article Text |
id | pubmed-6917497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69174972019-12-18 Predictors of SIV recrudescence following antiretroviral treatment interruption Pinkevych, Mykola Fennessey, Christine M Cromer, Deborah Reid, Carolyn Trubey, Charles M Lifson, Jeffrey D Keele, Brandon F Davenport, Miles P eLife Microbiology and Infectious Disease There is currently a need for proxy measures of the HIV rebound competent reservoir (RCR) that can predict viral rebound after combined antiretroviral treatment (cART) interruption. In this study, macaques infected with a barcoded SIVmac239 virus received cART beginning between 4- and 27 days post-infection, leading to the establishment of different levels of viral dissemination and persistence. Later treatment initiation led to higher SIV DNA levels maintained during treatment, which was significantly associated with an increased frequency of SIV reactivation and production of progeny capable of causing rebound viremia following treatment interruption. However, a 100-fold increase in SIV DNA in PBMCs was associated with only a 2-fold increase in the frequency of reactivation. These data suggest that the RCR can be established soon after infection, and that a large fraction of persistent viral DNA that accumulates after this time makes relatively little contribution to viral rebound. eLife Sciences Publications, Ltd 2019-10-25 /pmc/articles/PMC6917497/ /pubmed/31650954 http://dx.doi.org/10.7554/eLife.49022 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Microbiology and Infectious Disease Pinkevych, Mykola Fennessey, Christine M Cromer, Deborah Reid, Carolyn Trubey, Charles M Lifson, Jeffrey D Keele, Brandon F Davenport, Miles P Predictors of SIV recrudescence following antiretroviral treatment interruption |
title | Predictors of SIV recrudescence following antiretroviral treatment interruption |
title_full | Predictors of SIV recrudescence following antiretroviral treatment interruption |
title_fullStr | Predictors of SIV recrudescence following antiretroviral treatment interruption |
title_full_unstemmed | Predictors of SIV recrudescence following antiretroviral treatment interruption |
title_short | Predictors of SIV recrudescence following antiretroviral treatment interruption |
title_sort | predictors of siv recrudescence following antiretroviral treatment interruption |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917497/ https://www.ncbi.nlm.nih.gov/pubmed/31650954 http://dx.doi.org/10.7554/eLife.49022 |
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