Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.

Recent studies in the SIV-macaque model of HIV infection suggest that Nef-specific CD8+ T-cell responses may mediate highly effective immune control of viraemia. In HIV infection Nef recognition dominates in acute infection, but in large cohort studies of chronically infected subjects, breadth of T...

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Main Authors: Emily Adland, Jonathan M Carlson, Paolo Paioni, Henrik Kløverpris, Roger Shapiro, Anthony Ogwu, Lynn Riddell, Graz Luzzi, Fabian Chen, Thambiah Balachandran, David Heckerman, Anette Stryhn, Anne Edwards, Thumbi Ndung'u, Bruce D Walker, Søren Buus, Philip Goulder, Philippa C Matthews
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0073117
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author Emily Adland
Jonathan M Carlson
Paolo Paioni
Henrik Kløverpris
Roger Shapiro
Anthony Ogwu
Lynn Riddell
Graz Luzzi
Fabian Chen
Thambiah Balachandran
David Heckerman
Anette Stryhn
Anne Edwards
Thumbi Ndung'u
Bruce D Walker
Søren Buus
Philip Goulder
Philippa C Matthews
author_facet Emily Adland
Jonathan M Carlson
Paolo Paioni
Henrik Kløverpris
Roger Shapiro
Anthony Ogwu
Lynn Riddell
Graz Luzzi
Fabian Chen
Thambiah Balachandran
David Heckerman
Anette Stryhn
Anne Edwards
Thumbi Ndung'u
Bruce D Walker
Søren Buus
Philip Goulder
Philippa C Matthews
author_sort Emily Adland
collection DOAJ
description Recent studies in the SIV-macaque model of HIV infection suggest that Nef-specific CD8+ T-cell responses may mediate highly effective immune control of viraemia. In HIV infection Nef recognition dominates in acute infection, but in large cohort studies of chronically infected subjects, breadth of T cell responses to Nef has not been correlated with significant viraemic control. Improved disease outcomes have instead been associated with targeting Gag and, in some cases, Pol. However analyses of the breadth of Nef-specific T cell responses have been confounded by the extreme immunogenicity and multiple epitope overlap within the central regions of Nef, making discrimination of distinct responses impossible via IFN-gamma ELISPOT assays. Thus an alternative approach to assess Nef as an immune target is needed. Here, we show in a cohort of >700 individuals with chronic C-clade infection that >50% of HLA-B-selected polymorphisms within Nef are associated with a predicted fitness cost to the virus, and that HLA-B alleles that successfully drive selection within Nef are those linked with lower viral loads. Furthermore, the specific CD8+ T cell epitopes that are restricted by protective HLA Class I alleles correspond substantially to effective SIV-specific epitopes in Nef. Distinguishing such individual HIV-specific responses within Nef requires specific peptide-MHC I tetramers. Overall, these data suggest that CD8+ T cell targeting of certain specific Nef epitopes contributes to HIV suppression. These data suggest that a re-evaluation of the potential use of Nef in HIV T-cell vaccine candidates would be justified.
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spelling doaj-art-69e24ca61d674730944408fe0c33b9dd2025-08-20T02:22:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7311710.1371/journal.pone.0073117Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.Emily AdlandJonathan M CarlsonPaolo PaioniHenrik KløverprisRoger ShapiroAnthony OgwuLynn RiddellGraz LuzziFabian ChenThambiah BalachandranDavid HeckermanAnette StryhnAnne EdwardsThumbi Ndung'uBruce D WalkerSøren BuusPhilip GoulderPhilippa C MatthewsRecent studies in the SIV-macaque model of HIV infection suggest that Nef-specific CD8+ T-cell responses may mediate highly effective immune control of viraemia. In HIV infection Nef recognition dominates in acute infection, but in large cohort studies of chronically infected subjects, breadth of T cell responses to Nef has not been correlated with significant viraemic control. Improved disease outcomes have instead been associated with targeting Gag and, in some cases, Pol. However analyses of the breadth of Nef-specific T cell responses have been confounded by the extreme immunogenicity and multiple epitope overlap within the central regions of Nef, making discrimination of distinct responses impossible via IFN-gamma ELISPOT assays. Thus an alternative approach to assess Nef as an immune target is needed. Here, we show in a cohort of >700 individuals with chronic C-clade infection that >50% of HLA-B-selected polymorphisms within Nef are associated with a predicted fitness cost to the virus, and that HLA-B alleles that successfully drive selection within Nef are those linked with lower viral loads. Furthermore, the specific CD8+ T cell epitopes that are restricted by protective HLA Class I alleles correspond substantially to effective SIV-specific epitopes in Nef. Distinguishing such individual HIV-specific responses within Nef requires specific peptide-MHC I tetramers. Overall, these data suggest that CD8+ T cell targeting of certain specific Nef epitopes contributes to HIV suppression. These data suggest that a re-evaluation of the potential use of Nef in HIV T-cell vaccine candidates would be justified.https://doi.org/10.1371/journal.pone.0073117
spellingShingle Emily Adland
Jonathan M Carlson
Paolo Paioni
Henrik Kløverpris
Roger Shapiro
Anthony Ogwu
Lynn Riddell
Graz Luzzi
Fabian Chen
Thambiah Balachandran
David Heckerman
Anette Stryhn
Anne Edwards
Thumbi Ndung'u
Bruce D Walker
Søren Buus
Philip Goulder
Philippa C Matthews
Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
PLoS ONE
title Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
title_full Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
title_fullStr Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
title_full_unstemmed Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
title_short Nef-specific CD8+ T cell responses contribute to HIV-1 immune control.
title_sort nef specific cd8 t cell responses contribute to hiv 1 immune control
url https://doi.org/10.1371/journal.pone.0073117
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