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Anti-proliferative therapy for HIV cure: a compound interest approach
In the era of antiretroviral therapy (ART), HIV-1 infection is no longer tantamount to early death. Yet the benefits of treatment are available only to those who can access, afford, and tolerate taking daily pills. True cure is challenged by HIV latency, the ability of chromosomally integrated virus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479830/ https://www.ncbi.nlm.nih.gov/pubmed/28638104 http://dx.doi.org/10.1038/s41598-017-04160-3 |
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author | Reeves, Daniel B. Duke, Elizabeth R. Hughes, Sean M. Prlic, Martin Hladik, Florian Schiffer, Joshua T. |
author_facet | Reeves, Daniel B. Duke, Elizabeth R. Hughes, Sean M. Prlic, Martin Hladik, Florian Schiffer, Joshua T. |
author_sort | Reeves, Daniel B. |
collection | PubMed |
description | In the era of antiretroviral therapy (ART), HIV-1 infection is no longer tantamount to early death. Yet the benefits of treatment are available only to those who can access, afford, and tolerate taking daily pills. True cure is challenged by HIV latency, the ability of chromosomally integrated virus to persist within memory CD4(+) T cells in a non-replicative state and activate when ART is discontinued. Using a mathematical model of HIV dynamics, we demonstrate that treatment strategies offering modest but continual enhancement of reservoir clearance rates result in faster cure than abrupt, one-time reductions in reservoir size. We frame this concept in terms of compounding interest: small changes in interest rate drastically improve returns over time. On ART, latent cell proliferation rates are orders of magnitude larger than activation and new infection rates. Contingent on subtypes of cells that may make up the reservoir and their respective proliferation rates, our model predicts that coupling clinically available, anti-proliferative therapies with ART could result in functional cure within 2–10 years rather than several decades on ART alone. |
format | Online Article Text |
id | pubmed-5479830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54798302017-06-23 Anti-proliferative therapy for HIV cure: a compound interest approach Reeves, Daniel B. Duke, Elizabeth R. Hughes, Sean M. Prlic, Martin Hladik, Florian Schiffer, Joshua T. Sci Rep Article In the era of antiretroviral therapy (ART), HIV-1 infection is no longer tantamount to early death. Yet the benefits of treatment are available only to those who can access, afford, and tolerate taking daily pills. True cure is challenged by HIV latency, the ability of chromosomally integrated virus to persist within memory CD4(+) T cells in a non-replicative state and activate when ART is discontinued. Using a mathematical model of HIV dynamics, we demonstrate that treatment strategies offering modest but continual enhancement of reservoir clearance rates result in faster cure than abrupt, one-time reductions in reservoir size. We frame this concept in terms of compounding interest: small changes in interest rate drastically improve returns over time. On ART, latent cell proliferation rates are orders of magnitude larger than activation and new infection rates. Contingent on subtypes of cells that may make up the reservoir and their respective proliferation rates, our model predicts that coupling clinically available, anti-proliferative therapies with ART could result in functional cure within 2–10 years rather than several decades on ART alone. Nature Publishing Group UK 2017-06-21 /pmc/articles/PMC5479830/ /pubmed/28638104 http://dx.doi.org/10.1038/s41598-017-04160-3 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Reeves, Daniel B. Duke, Elizabeth R. Hughes, Sean M. Prlic, Martin Hladik, Florian Schiffer, Joshua T. Anti-proliferative therapy for HIV cure: a compound interest approach |
title | Anti-proliferative therapy for HIV cure: a compound interest approach |
title_full | Anti-proliferative therapy for HIV cure: a compound interest approach |
title_fullStr | Anti-proliferative therapy for HIV cure: a compound interest approach |
title_full_unstemmed | Anti-proliferative therapy for HIV cure: a compound interest approach |
title_short | Anti-proliferative therapy for HIV cure: a compound interest approach |
title_sort | anti-proliferative therapy for hiv cure: a compound interest approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479830/ https://www.ncbi.nlm.nih.gov/pubmed/28638104 http://dx.doi.org/10.1038/s41598-017-04160-3 |
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