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HIV-1 DNA predicts disease progression and post-treatment virological control

In HIV-1 infection, a population of latently infected cells facilitates viral persistence despite antiretroviral therapy (ART). With the aim of identifying individuals in whom ART might induce a period of viraemic control on stopping therapy, we hypothesised that quantification of the pool of latent...

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Detalles Bibliográficos
Autores principales: Williams, James P, Hurst, Jacob, Stöhr, Wolfgang, Robinson, Nicola, Brown, Helen, Fisher, Martin, Kinloch, Sabine, Cooper, David, Schechter, Mauro, Tambussi, Giuseppe, Fidler, Sarah, Carrington, Mary, Babiker, Abdel, Weber, Jonathan, Koelsch, Kersten K, Kelleher, Anthony D, Phillips, Rodney E, Frater, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199415/
https://www.ncbi.nlm.nih.gov/pubmed/25217531
http://dx.doi.org/10.7554/eLife.03821
Descripción
Sumario:In HIV-1 infection, a population of latently infected cells facilitates viral persistence despite antiretroviral therapy (ART). With the aim of identifying individuals in whom ART might induce a period of viraemic control on stopping therapy, we hypothesised that quantification of the pool of latently infected cells in primary HIV-1 infection (PHI) would predict clinical progression and viral replication following ART. We measured HIV-1 DNA in a highly characterised randomised population of individuals with PHI. We explored associations between HIV-1 DNA and immunological and virological markers of clinical progression, including viral rebound in those interrupting therapy. In multivariable analyses, HIV-1 DNA was more predictive of disease progression than plasma viral load and, at treatment interruption, predicted time to plasma virus rebound. HIV-1 DNA may help identify individuals who could safely interrupt ART in future HIV-1 eradication trials. Clinical trial registration: ISRCTN76742797 and EudraCT2004-000446-20 DOI: http://dx.doi.org/10.7554/eLife.03821.001