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The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children
As the immune system develops with age, children combat infections better. HIV-1, however, targets an activated immune system, potentially rendering children increasingly permissive to HIV-1 infection as they grow. How HIV-1 fitness changes with age in children is unknown. Here, we estimated the wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862260/ https://www.ncbi.nlm.nih.gov/pubmed/33542308 http://dx.doi.org/10.1038/s41598-021-82293-2 |
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author | Nagaraja, Pradeep Gopalan, Bindu P. D’Souza, Reena R. Sarkar, Debolina Rajnala, Niharika Dixit, Narendra M. Shet, Anita |
author_facet | Nagaraja, Pradeep Gopalan, Bindu P. D’Souza, Reena R. Sarkar, Debolina Rajnala, Niharika Dixit, Narendra M. Shet, Anita |
author_sort | Nagaraja, Pradeep |
collection | PubMed |
description | As the immune system develops with age, children combat infections better. HIV-1, however, targets an activated immune system, potentially rendering children increasingly permissive to HIV-1 infection as they grow. How HIV-1 fitness changes with age in children is unknown. Here, we estimated the within-host basic reproductive ratio, R(0), a marker of viral fitness, in HIV-1 subtype C-infected children in India, aged between 84 days and 17 years. We measured serial viral load and CD4 T cell counts in 171 children who initiated first-line ART. For 25 children, regular and frequent measurements provided adequate data points for analysis using a mathematical model of viral dynamics to estimate R(0). For the rest, we used CD4 counts for approximate estimation of R(0). The viral load decline during therapy was biphasic. The mean lifespans of productively and long-lived infected cells were 1.4 and 27.8 days, respectively. The mean R(0) was 1.5 in children aged < 5 years, increased with age, and approached 6.0 at 18 years, close to 5.8 estimated previously for adults. The tolerogenic immune environment thus compromises HIV-1 fitness in young children. Early treatment initiation, when the R(0) is small, will likely improve viral control, in addition to suppressing the latent reservoir. |
format | Online Article Text |
id | pubmed-7862260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78622602021-02-05 The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children Nagaraja, Pradeep Gopalan, Bindu P. D’Souza, Reena R. Sarkar, Debolina Rajnala, Niharika Dixit, Narendra M. Shet, Anita Sci Rep Article As the immune system develops with age, children combat infections better. HIV-1, however, targets an activated immune system, potentially rendering children increasingly permissive to HIV-1 infection as they grow. How HIV-1 fitness changes with age in children is unknown. Here, we estimated the within-host basic reproductive ratio, R(0), a marker of viral fitness, in HIV-1 subtype C-infected children in India, aged between 84 days and 17 years. We measured serial viral load and CD4 T cell counts in 171 children who initiated first-line ART. For 25 children, regular and frequent measurements provided adequate data points for analysis using a mathematical model of viral dynamics to estimate R(0). For the rest, we used CD4 counts for approximate estimation of R(0). The viral load decline during therapy was biphasic. The mean lifespans of productively and long-lived infected cells were 1.4 and 27.8 days, respectively. The mean R(0) was 1.5 in children aged < 5 years, increased with age, and approached 6.0 at 18 years, close to 5.8 estimated previously for adults. The tolerogenic immune environment thus compromises HIV-1 fitness in young children. Early treatment initiation, when the R(0) is small, will likely improve viral control, in addition to suppressing the latent reservoir. Nature Publishing Group UK 2021-02-04 /pmc/articles/PMC7862260/ /pubmed/33542308 http://dx.doi.org/10.1038/s41598-021-82293-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nagaraja, Pradeep Gopalan, Bindu P. D’Souza, Reena R. Sarkar, Debolina Rajnala, Niharika Dixit, Narendra M. Shet, Anita The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title | The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title_full | The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title_fullStr | The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title_full_unstemmed | The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title_short | The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children |
title_sort | within-host fitness of hiv-1 increases with age in art-naïve hiv-1 subtype c infected children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862260/ https://www.ncbi.nlm.nih.gov/pubmed/33542308 http://dx.doi.org/10.1038/s41598-021-82293-2 |
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