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Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller
HIV-1 controllers are patients who control HIV-1 viral replication without antiretroviral therapy. Control is achieved very early in the course of infection, but the mechanisms through which viral replication is restricted are not fully understood. We describe a patient who presented with acute HIV-...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474502/ https://www.ncbi.nlm.nih.gov/pubmed/28159573 http://dx.doi.org/10.1016/j.ebiom.2017.01.034 |
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author | Walker-Sperling, Victoria E. Pohlmeyer, Christopher W. Veenhuis, Rebecca T. May, Megan Luna, Krystle A. Kirkpatrick, Allison R. Laeyendecker, Oliver Cox, Andrea L. Carrington, Mary Bailey, Justin R. Arduino, Roberto C. Blankson, Joel N. |
author_facet | Walker-Sperling, Victoria E. Pohlmeyer, Christopher W. Veenhuis, Rebecca T. May, Megan Luna, Krystle A. Kirkpatrick, Allison R. Laeyendecker, Oliver Cox, Andrea L. Carrington, Mary Bailey, Justin R. Arduino, Roberto C. Blankson, Joel N. |
author_sort | Walker-Sperling, Victoria E. |
collection | PubMed |
description | HIV-1 controllers are patients who control HIV-1 viral replication without antiretroviral therapy. Control is achieved very early in the course of infection, but the mechanisms through which viral replication is restricted are not fully understood. We describe a patient who presented with acute HIV-1 infection and was found to have an HIV-1 RNA level of < 100 copies/mL. She did not have any known protective HLA alleles, but significant immune activation of CD8 + T cells and natural killer (NK) cells was present, and both cell types inhibited viral replication. Virus cultured from this patient replicated as well in vitro as virus isolated from her partner, a patient with AIDS who was the source of transmission. Virologic breakthrough occurred 9 months after her initial presentation and was associated with an increase in CD4 + T cell activation levels and a significant decrease in NK cell inhibitory capacity. Remarkably, CD8 + T cell inhibitory capacity was preserved and there were no new escape mutations in targeted Gag epitopes. These findings suggest that fully replication-competent virus can be controlled in acute HIV-1 infection in some patients without protective HLA alleles and that NK cell responses may contribute to this early control of viral replication. |
format | Online Article Text |
id | pubmed-5474502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54745022017-06-26 Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller Walker-Sperling, Victoria E. Pohlmeyer, Christopher W. Veenhuis, Rebecca T. May, Megan Luna, Krystle A. Kirkpatrick, Allison R. Laeyendecker, Oliver Cox, Andrea L. Carrington, Mary Bailey, Justin R. Arduino, Roberto C. Blankson, Joel N. EBioMedicine Research Paper HIV-1 controllers are patients who control HIV-1 viral replication without antiretroviral therapy. Control is achieved very early in the course of infection, but the mechanisms through which viral replication is restricted are not fully understood. We describe a patient who presented with acute HIV-1 infection and was found to have an HIV-1 RNA level of < 100 copies/mL. She did not have any known protective HLA alleles, but significant immune activation of CD8 + T cells and natural killer (NK) cells was present, and both cell types inhibited viral replication. Virus cultured from this patient replicated as well in vitro as virus isolated from her partner, a patient with AIDS who was the source of transmission. Virologic breakthrough occurred 9 months after her initial presentation and was associated with an increase in CD4 + T cell activation levels and a significant decrease in NK cell inhibitory capacity. Remarkably, CD8 + T cell inhibitory capacity was preserved and there were no new escape mutations in targeted Gag epitopes. These findings suggest that fully replication-competent virus can be controlled in acute HIV-1 infection in some patients without protective HLA alleles and that NK cell responses may contribute to this early control of viral replication. Elsevier 2017-01-26 /pmc/articles/PMC5474502/ /pubmed/28159573 http://dx.doi.org/10.1016/j.ebiom.2017.01.034 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Walker-Sperling, Victoria E. Pohlmeyer, Christopher W. Veenhuis, Rebecca T. May, Megan Luna, Krystle A. Kirkpatrick, Allison R. Laeyendecker, Oliver Cox, Andrea L. Carrington, Mary Bailey, Justin R. Arduino, Roberto C. Blankson, Joel N. Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title | Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title_full | Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title_fullStr | Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title_full_unstemmed | Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title_short | Factors Associated With the Control of Viral Replication and Virologic Breakthrough in a Recently Infected HIV-1 Controller |
title_sort | factors associated with the control of viral replication and virologic breakthrough in a recently infected hiv-1 controller |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474502/ https://www.ncbi.nlm.nih.gov/pubmed/28159573 http://dx.doi.org/10.1016/j.ebiom.2017.01.034 |
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