Cargando…
Analysis of ex vivo HIV-1 infection in a controller-discordant couple
OBJECTIVES: Elite controllers (EC) are a rare group of individuals living with HIV-1 who naturally control HIV-1 replication to levels below the limit of detection without antiretroviral therapy (ART) and rarely progress to AIDS. The mechanisms contributing to this control remain incompletely elucid...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mediscript Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038135/ https://www.ncbi.nlm.nih.gov/pubmed/30050679 |
_version_ | 1783338435478552576 |
---|---|
author | Madlala, Paradise Van de Velde, Paulien Van Remoortel, Barbara Vets, Sofie Van Wijngaerden, Eric Van Laethem, Kristel Gijsbers, Rik Schrijvers, Rik Debyser, Zeger |
author_facet | Madlala, Paradise Van de Velde, Paulien Van Remoortel, Barbara Vets, Sofie Van Wijngaerden, Eric Van Laethem, Kristel Gijsbers, Rik Schrijvers, Rik Debyser, Zeger |
author_sort | Madlala, Paradise |
collection | PubMed |
description | OBJECTIVES: Elite controllers (EC) are a rare group of individuals living with HIV-1 who naturally control HIV-1 replication to levels below the limit of detection without antiretroviral therapy (ART) and rarely progress to AIDS. The mechanisms contributing to this control remain incompletely elucidated. In the present study, we have assessed whether cellular host factors could modulate HIV-1 replication post-entry in a controller-discordant couple living with HIV-1. METHODS: CD4 T cells from a controller-discordant couple, one partner being an EC and the other an HIV-1 progressor (PR), and healthy controls (HC) were isolated, activated and infected with VSV-G pseudotyped yellow fluorescent protein-encoding single-round HIV-1 virus (HIV-YFP). Viral reverse transcripts, 2-LTR circles and integrated proviral HIV-1 DNA were monitored by quantitative PCR (qPCR) and integration sites were analysed. We further measured LEDGF/p75 and p21 mRNA expression levels by qPCR. RESULTS: Infection of activated CD4 T cells with HIV-YFP was reduced in EC compared with the PR partner, and HC. Evaluation of viral DNA forms suggested a block after entry and during the early steps of HIV-1 reverse transcription in EC. The integration site distribution pattern in EC, PR and HC was similar. The p21 expression in CD4 T cells of EC was elevated compared with the PR or HC, in line with previous work. CONCLUSIONS: Our study suggests a reduced permissiveness to HIV-1 infection of CD4 T cells from EC due to a block of HIV-1 replication after entry and before integration that might contribute to the EC phenotype in our patient. |
format | Online Article Text |
id | pubmed-6038135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mediscript Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60381352018-07-26 Analysis of ex vivo HIV-1 infection in a controller-discordant couple Madlala, Paradise Van de Velde, Paulien Van Remoortel, Barbara Vets, Sofie Van Wijngaerden, Eric Van Laethem, Kristel Gijsbers, Rik Schrijvers, Rik Debyser, Zeger J Virus Erad Original Research OBJECTIVES: Elite controllers (EC) are a rare group of individuals living with HIV-1 who naturally control HIV-1 replication to levels below the limit of detection without antiretroviral therapy (ART) and rarely progress to AIDS. The mechanisms contributing to this control remain incompletely elucidated. In the present study, we have assessed whether cellular host factors could modulate HIV-1 replication post-entry in a controller-discordant couple living with HIV-1. METHODS: CD4 T cells from a controller-discordant couple, one partner being an EC and the other an HIV-1 progressor (PR), and healthy controls (HC) were isolated, activated and infected with VSV-G pseudotyped yellow fluorescent protein-encoding single-round HIV-1 virus (HIV-YFP). Viral reverse transcripts, 2-LTR circles and integrated proviral HIV-1 DNA were monitored by quantitative PCR (qPCR) and integration sites were analysed. We further measured LEDGF/p75 and p21 mRNA expression levels by qPCR. RESULTS: Infection of activated CD4 T cells with HIV-YFP was reduced in EC compared with the PR partner, and HC. Evaluation of viral DNA forms suggested a block after entry and during the early steps of HIV-1 reverse transcription in EC. The integration site distribution pattern in EC, PR and HC was similar. The p21 expression in CD4 T cells of EC was elevated compared with the PR or HC, in line with previous work. CONCLUSIONS: Our study suggests a reduced permissiveness to HIV-1 infection of CD4 T cells from EC due to a block of HIV-1 replication after entry and before integration that might contribute to the EC phenotype in our patient. Mediscript Ltd 2018-07-01 /pmc/articles/PMC6038135/ /pubmed/30050679 Text en © 2018 The Authors. Journal of Virus Eradication published by Mediscript Ltd http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article published under the terms of a Creative Commons License. |
spellingShingle | Original Research Madlala, Paradise Van de Velde, Paulien Van Remoortel, Barbara Vets, Sofie Van Wijngaerden, Eric Van Laethem, Kristel Gijsbers, Rik Schrijvers, Rik Debyser, Zeger Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title | Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title_full | Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title_fullStr | Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title_full_unstemmed | Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title_short | Analysis of ex vivo HIV-1 infection in a controller-discordant couple |
title_sort | analysis of ex vivo hiv-1 infection in a controller-discordant couple |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038135/ https://www.ncbi.nlm.nih.gov/pubmed/30050679 |
work_keys_str_mv | AT madlalaparadise analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT vandeveldepaulien analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT vanremoortelbarbara analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT vetssofie analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT vanwijngaerdeneric analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT vanlaethemkristel analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT gijsbersrik analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT schrijversrik analysisofexvivohiv1infectioninacontrollerdiscordantcouple AT debyserzeger analysisofexvivohiv1infectioninacontrollerdiscordantcouple |