Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.

In the present study, we analyzed the functional profile of CD8+ T-cell responses directed against autologous transmitted/founder HIV-1 isolates during acute and early infection, and examined whether multifunctionality is required for selection of virus escape mutations. Seven anti-retroviral therap...

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Главные авторы: Ferrari, G, Korber, B, Goonetilleke, N, Liu, M, Turnbull, E, Salazar-Gonzalez, J, Hawkins, N, Self, S, Watson, S, Betts, MR, Gay, C, McGhee, K, Pellegrino, P, Williams, I, Tomaras, G, Haynes, B, Gray, C, Borrow, P, Roederer, M, Mcmichael, A, Weinhold, K
Формат: Journal article
Язык:English
Опубликовано: Public Library of Science 2011
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author Ferrari, G
Korber, B
Goonetilleke, N
Liu, M
Turnbull, E
Salazar-Gonzalez, J
Hawkins, N
Self, S
Watson, S
Betts, MR
Gay, C
McGhee, K
Pellegrino, P
Williams, I
Tomaras, G
Haynes, B
Gray, C
Borrow, P
Roederer, M
Mcmichael, A
Weinhold, K
author_facet Ferrari, G
Korber, B
Goonetilleke, N
Liu, M
Turnbull, E
Salazar-Gonzalez, J
Hawkins, N
Self, S
Watson, S
Betts, MR
Gay, C
McGhee, K
Pellegrino, P
Williams, I
Tomaras, G
Haynes, B
Gray, C
Borrow, P
Roederer, M
Mcmichael, A
Weinhold, K
author_sort Ferrari, G
collection OXFORD
description In the present study, we analyzed the functional profile of CD8+ T-cell responses directed against autologous transmitted/founder HIV-1 isolates during acute and early infection, and examined whether multifunctionality is required for selection of virus escape mutations. Seven anti-retroviral therapy-naïve subjects were studied in detail between 1 and 87 weeks following onset of symptoms of acute HIV-1 infection. Synthetic peptides representing the autologous transmitted/founder HIV-1 sequences were used in multiparameter flow cytometry assays to determine the functionality of HIV-1-specific CD8+ T memory cells. In all seven patients, the earliest T cell responses were predominantly oligofunctional, although the relative contribution of multifunctional cell responses increased significantly with time from infection. Interestingly, only the magnitude of the total and not of the poly-functional T-cell responses was significantly associated with the selection of escape mutants. However, the high contribution of MIP-1β-producing CD8+ T-cells to the total response suggests that mechanisms not limited to cytotoxicity could be exerting immune pressure during acute infection. Lastly, we show that epitope entropy, reflecting the capacity of the epitope to tolerate mutational change and defined as the diversity of epitope sequences at the population level, was also correlated with rate of emergence of escape mutants.
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spelling oxford-uuid:75b4a862-44d2-47b2-a7f8-0d576bd8ac902022-03-26T20:11:09ZRelationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:75b4a862-44d2-47b2-a7f8-0d576bd8ac90EnglishSymplectic Elements at OxfordPublic Library of Science2011Ferrari, GKorber, BGoonetilleke, NLiu, MTurnbull, ESalazar-Gonzalez, JHawkins, NSelf, SWatson, SBetts, MRGay, CMcGhee, KPellegrino, PWilliams, ITomaras, GHaynes, BGray, CBorrow, PRoederer, MMcmichael, AWeinhold, KIn the present study, we analyzed the functional profile of CD8+ T-cell responses directed against autologous transmitted/founder HIV-1 isolates during acute and early infection, and examined whether multifunctionality is required for selection of virus escape mutations. Seven anti-retroviral therapy-naïve subjects were studied in detail between 1 and 87 weeks following onset of symptoms of acute HIV-1 infection. Synthetic peptides representing the autologous transmitted/founder HIV-1 sequences were used in multiparameter flow cytometry assays to determine the functionality of HIV-1-specific CD8+ T memory cells. In all seven patients, the earliest T cell responses were predominantly oligofunctional, although the relative contribution of multifunctional cell responses increased significantly with time from infection. Interestingly, only the magnitude of the total and not of the poly-functional T-cell responses was significantly associated with the selection of escape mutants. However, the high contribution of MIP-1β-producing CD8+ T-cells to the total response suggests that mechanisms not limited to cytotoxicity could be exerting immune pressure during acute infection. Lastly, we show that epitope entropy, reflecting the capacity of the epitope to tolerate mutational change and defined as the diversity of epitope sequences at the population level, was also correlated with rate of emergence of escape mutants.
spellingShingle Ferrari, G
Korber, B
Goonetilleke, N
Liu, M
Turnbull, E
Salazar-Gonzalez, J
Hawkins, N
Self, S
Watson, S
Betts, MR
Gay, C
McGhee, K
Pellegrino, P
Williams, I
Tomaras, G
Haynes, B
Gray, C
Borrow, P
Roederer, M
Mcmichael, A
Weinhold, K
Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title_full Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title_fullStr Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title_full_unstemmed Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title_short Relationship between functional profile of HIV-1 specific CD8 T cells and epitope variability with the selection of escape mutants in acute HIV-1 infection.
title_sort relationship between functional profile of hiv 1 specific cd8 t cells and epitope variability with the selection of escape mutants in acute hiv 1 infection
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