HIV reservoirs: what, where and how to target them
Viral reservoirs pose a major challenge in the efforts towards curing HIV. Here, Churchill, Deeks, Margolis, Siliciano and Swanstrom discuss the cells and tissues that constitute the viral reservoir, how best to measure it and how to target this source of persistent infection. One of the main challe...
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Published in | Nature reviews. Microbiology Vol. 14; no. 1; pp. 55 - 60 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.01.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Abstract | Viral reservoirs pose a major challenge in the efforts towards curing HIV. Here, Churchill, Deeks, Margolis, Siliciano and Swanstrom discuss the cells and tissues that constitute the viral reservoir, how best to measure it and how to target this source of persistent infection.
One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours integrated, replication-competent provirus within host cellular DNA. This reservoir is resistant to antiretroviral therapy (ART) and to clearance by the immune system of the host; viruses originating from this reservoir lead to rebound viraemia once treatment is stopped, giving rise to new rounds of infection. Several studies have focused on elucidating the cells and tissues that harbour persistent virus, the true size of the reservoir and how best to target it, but these topics are the subject of ongoing debate. In this Viewpoint article, several experts in the field discuss the constitution of the viral reservoir, how best to measure it and the best ways to target this source of persistent infection. |
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AbstractList | One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours integrated, replication-competent provirus within host cellular DNA. This reservoir is resistant to antiretroviral therapy (ART) and to clearance by the immune system of the host; viruses originating from this reservoir lead to rebound viraemia once treatment is stopped, giving rise to new rounds of infection. Several studies have focused on elucidating the cells and tissues that harbour persistent virus, the true size of the reservoir and how best to target it, but these topics are the subject of ongoing debate. In this Viewpoint article, several experts in the field discuss the constitution of the viral reservoir, how best to measure it and the best ways to target this source of persistent infection.One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours integrated, replication-competent provirus within host cellular DNA. This reservoir is resistant to antiretroviral therapy (ART) and to clearance by the immune system of the host; viruses originating from this reservoir lead to rebound viraemia once treatment is stopped, giving rise to new rounds of infection. Several studies have focused on elucidating the cells and tissues that harbour persistent virus, the true size of the reservoir and how best to target it, but these topics are the subject of ongoing debate. In this Viewpoint article, several experts in the field discuss the constitution of the viral reservoir, how best to measure it and the best ways to target this source of persistent infection. One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours integrated, replication-competent provirus within host cellular DNA. This reservoir is resistant to antiretroviral therapy (ART) and to clearance by the immune system of the host; viruses originating from this reservoir lead to rebound viraemia once treatment is stopped, giving rise to new rounds of infection. Several studies have focused on elucidating the cells and tissues that harbour persistent virus, the true size of the reservoir and how best to target it, but these topics are the subject of ongoing debate. In this Viewpoint article, several experts in the field discuss the constitution of the viral reservoir, how best to measure it and the best ways to target this source of persistent infection. Viral reservoirs pose a major challenge in the efforts towards curing HIV. Here, Churchill, Deeks, Margolis, Siliciano and Swanstrom discuss the cells and tissues that constitute the viral reservoir, how best to measure it and how to target this source of persistent infection. One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours integrated, replication-competent provirus within host cellular DNA. This reservoir is resistant to antiretroviral therapy (ART) and to clearance by the immune system of the host; viruses originating from this reservoir lead to rebound viraemia once treatment is stopped, giving rise to new rounds of infection. Several studies have focused on elucidating the cells and tissues that harbour persistent virus, the true size of the reservoir and how best to target it, but these topics are the subject of ongoing debate. In this Viewpoint article, several experts in the field discuss the constitution of the viral reservoir, how best to measure it and the best ways to target this source of persistent infection. |
Audience | Academic |
Author | Siliciano, Robert F. Margolis, David M. Churchill, Melissa J. Swanstrom, Ronald Deeks, Steven G. |
Author_xml | – sequence: 1 givenname: Melissa J. surname: Churchill fullname: Churchill, Melissa J. email: churchil@burnet.edu.au organization: Melissa J. Churchill is at the Centre for Biomedical Research, Burnet Institute, Melbourne, Victoria 3004, Australia – sequence: 2 givenname: Steven G. surname: Deeks fullname: Deeks, Steven G. email: steven.deeks@ucsf.edu organization: Steven G. Deeks is at the Department of Medicine, University of California, San Francisco, California 94110, USA – sequence: 3 givenname: David M. surname: Margolis fullname: Margolis, David M. email: dmargo@med.unc.edu organization: and the Department of Medicine, David M. Margolis is at the University of North Carolina (UNC) HIV Cure Center, Institute of Global Health and Infectious Diseases, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA – sequence: 4 givenname: Robert F. surname: Siliciano fullname: Siliciano, Robert F. email: rsiliciano@jhmi.edu organization: Robert F. Siliciano is at the Department of Medicine and Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA – sequence: 5 givenname: Ronald surname: Swanstrom fullname: Swanstrom, Ronald email: ron_swanstrom@med.unc.edu organization: the Department of Biochemistry and Biophysics, Ronald Swanstrom is at the Lineberger Comprehensive Cancer Center, and the University of North Carolina (UNC) Center for AIDS Research, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26616417$$D View this record in MEDLINE/PubMed |
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Snippet | Viral reservoirs pose a major challenge in the efforts towards curing HIV. Here, Churchill, Deeks, Margolis, Siliciano and Swanstrom discuss the cells and... One of the main challenges in the fight against HIV infection is to develop strategies that are able to eliminate the persistent viral reservoir that harbours... |
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SubjectTerms | 631/250/255/1901 631/326/596/1787 631/326/596/2564 Anti-HIV Agents - therapeutic use Antiretroviral agents Beliefs, opinions and attitudes Biomedical and Life Sciences Care and treatment Complications and side effects Development and progression Health aspects Highly active antiretroviral therapy HIV - drug effects HIV - physiology HIV infections HIV Infections - drug therapy HIV Infections - virology Host-virus relationships Human immunodeficiency virus Humans Immune system Infectious Diseases Life Sciences Medical Microbiology Medical research Methods Microbiology Models, Animal Molecular targeted therapy Observations Parasitology Patient outcomes Physicians Proviruses - drug effects Proviruses - physiology viewpoint Virology Virulence (Microbiology) Virus Integration Virus Latency - drug effects |
Title | HIV reservoirs: what, where and how to target them |
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