Predicting the outcomes of treatment to eradicate the latent reservoir for HIV-1
Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency-reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4⁺ T cells, but the...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2014-09, Vol.111 (37), p.13475-13480 |
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creator | Hill, Alison L. Rosenbloom, Daniel I. S. Fu, Feng Nowak, Martin A. Siliciano, Robert F. |
description | Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency-reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4⁺ T cells, but the degree of reservoir reduction needed for cure remains unknown. Here we use a stochastic model of infection dynamics to estimate the efficacy of LRA needed to prevent viral rebound after ART interruption. We incorporate clinical data to estimate population-level parameter distributions and outcomes. Our findings suggest that ~2,000-fold reductions are required to permit a majority of patients to interrupt ART for 1 y without rebound and that rebound may occur suddenly after multiple years. Greater than 10,000-fold reductions may be required to prevent rebound altogether. Our results predict large variation in rebound times following LRA therapy, which will complicate clinical management. This model provides benchmarks for moving LRAs from the laboratory to the clinic and can aid in the design and interpretation of clinical trials. These results also apply to other interventions to reduce the latent reservoir and can explain the observed return of viremia after months of apparent cure in recent bone marrow transplant recipients and an immediately-treated neonate. |
doi_str_mv | 10.1073/pnas.1406663111 |
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S. ; Fu, Feng ; Nowak, Martin A. ; Siliciano, Robert F.</creator><creatorcontrib>Hill, Alison L. ; Rosenbloom, Daniel I. S. ; Fu, Feng ; Nowak, Martin A. ; Siliciano, Robert F.</creatorcontrib><description>Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency-reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4⁺ T cells, but the degree of reservoir reduction needed for cure remains unknown. Here we use a stochastic model of infection dynamics to estimate the efficacy of LRA needed to prevent viral rebound after ART interruption. We incorporate clinical data to estimate population-level parameter distributions and outcomes. Our findings suggest that ~2,000-fold reductions are required to permit a majority of patients to interrupt ART for 1 y without rebound and that rebound may occur suddenly after multiple years. Greater than 10,000-fold reductions may be required to prevent rebound altogether. Our results predict large variation in rebound times following LRA therapy, which will complicate clinical management. This model provides benchmarks for moving LRAs from the laboratory to the clinic and can aid in the design and interpretation of clinical trials. These results also apply to other interventions to reduce the latent reservoir and can explain the observed return of viremia after months of apparent cure in recent bone marrow transplant recipients and an immediately-treated neonate.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1406663111</identifier><identifier>PMID: 25097264</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>antiretroviral agents ; Antiretroviral drugs ; Antiretrovirals ; Benchmarks ; Biological Sciences ; Bone marrow ; case studies ; Cells ; clinical trials ; Disease Eradication ; Disease Reservoirs - virology ; drugs ; HIV ; HIV 1 ; HIV infections ; HIV Infections - therapy ; HIV Infections - virology ; HIV-1 - physiology ; Human immunodeficiency virus ; Human immunodeficiency virus 1 ; Humans ; Infections ; mathematical models ; Medical cures ; Modeling ; Models, Biological ; Parametric models ; Physical Sciences ; prediction ; remission ; Stem cells ; Stochastic Processes ; T lymphocytes ; Time Factors ; Transplants & implants ; Treatment Outcome ; Uncertainty ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (37), p.13475-13480</ispartof><rights>copyright © 1993–2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Sep 16, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c600t-f480cfbe510cc08a13e2b9a97a379f30431b16db57a501bad871439d7cf284363</citedby><cites>FETCH-LOGICAL-c600t-f480cfbe510cc08a13e2b9a97a379f30431b16db57a501bad871439d7cf284363</cites><orcidid>0000-0003-1413-3907</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/111/37.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43043494$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43043494$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27903,27904,53769,53771,57995,58228</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25097264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hill, Alison L.</creatorcontrib><creatorcontrib>Rosenbloom, Daniel I. S.</creatorcontrib><creatorcontrib>Fu, Feng</creatorcontrib><creatorcontrib>Nowak, Martin A.</creatorcontrib><creatorcontrib>Siliciano, Robert F.</creatorcontrib><title>Predicting the outcomes of treatment to eradicate the latent reservoir for HIV-1</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency-reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4⁺ T cells, but the degree of reservoir reduction needed for cure remains unknown. Here we use a stochastic model of infection dynamics to estimate the efficacy of LRA needed to prevent viral rebound after ART interruption. We incorporate clinical data to estimate population-level parameter distributions and outcomes. Our findings suggest that ~2,000-fold reductions are required to permit a majority of patients to interrupt ART for 1 y without rebound and that rebound may occur suddenly after multiple years. Greater than 10,000-fold reductions may be required to prevent rebound altogether. Our results predict large variation in rebound times following LRA therapy, which will complicate clinical management. This model provides benchmarks for moving LRAs from the laboratory to the clinic and can aid in the design and interpretation of clinical trials. 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S.</au><au>Fu, Feng</au><au>Nowak, Martin A.</au><au>Siliciano, Robert F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predicting the outcomes of treatment to eradicate the latent reservoir for HIV-1</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2014-09-16</date><risdate>2014</risdate><volume>111</volume><issue>37</issue><spage>13475</spage><epage>13480</epage><pages>13475-13480</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency-reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4⁺ T cells, but the degree of reservoir reduction needed for cure remains unknown. Here we use a stochastic model of infection dynamics to estimate the efficacy of LRA needed to prevent viral rebound after ART interruption. We incorporate clinical data to estimate population-level parameter distributions and outcomes. Our findings suggest that ~2,000-fold reductions are required to permit a majority of patients to interrupt ART for 1 y without rebound and that rebound may occur suddenly after multiple years. Greater than 10,000-fold reductions may be required to prevent rebound altogether. Our results predict large variation in rebound times following LRA therapy, which will complicate clinical management. This model provides benchmarks for moving LRAs from the laboratory to the clinic and can aid in the design and interpretation of clinical trials. 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subjects | antiretroviral agents Antiretroviral drugs Antiretrovirals Benchmarks Biological Sciences Bone marrow case studies Cells clinical trials Disease Eradication Disease Reservoirs - virology drugs HIV HIV 1 HIV infections HIV Infections - therapy HIV Infections - virology HIV-1 - physiology Human immunodeficiency virus Human immunodeficiency virus 1 Humans Infections mathematical models Medical cures Modeling Models, Biological Parametric models Physical Sciences prediction remission Stem cells Stochastic Processes T lymphocytes Time Factors Transplants & implants Treatment Outcome Uncertainty Viruses |
title | Predicting the outcomes of treatment to eradicate the latent reservoir for HIV-1 |
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