Differential clade-specific HLA-B*3501 association with HIV-1 disease outcome is linked to immunogenicity of a single Gag epitope.

TitleDifferential clade-specific HLA-B*3501 association with HIV-1 disease outcome is linked to immunogenicity of a single Gag epitope.
Publication TypeJournal Article
Year of Publication2012
AuthorsMatthews PC, Koyanagi M, Kløverpris HN, Harndahl M, Stryhn A, Akahoshi T, Gatanaga H, Oka S, Molina C J, Ponce H V, Avila Rios S, Cole D, Carlson JM, Payne RP, Ogwu A, Bere A, Ndung'u T, Gounder K, Chen F, Riddell L, Luzzi G, Shapiro R, Brander C, Walker BD, Sewell AK, Reyes Teran G, Heckerman D, Hunter E, Buus S, Takiguchi M, Goulder PJR
JournalJ Virol
Date Published2012 Sep 12
ISSN1098-5514
Abstract

The strongest genetic influence on immune control in HIV-1 infection is HLA class I genotype. Rapid disease progression in B-clade infection has been linked to HLA-B*35 expression, in particular to the less common HLA-B*3502 and HLA-B*3503 subtypes, but also to the most prevalent subtype, HLA-B*3501. In these studies we first demonstrate that, whereas HLA-B*3501 is associated with high viral setpoint in two further B-clade infected cohorts, in Japan and Mexico, this association does not hold in two large C-clade infected African cohorts. We tested the hypothesis that clade-specific differences in HLA associations with disease outcomes may be related to distinct targeting of critical CD8+ T-cell epitopes. We observed that only one epitope was significantly targeted differentially, namely, the Gag-specific epitope, NPPIPVGDIY ('NY10' , Gag 253-262, p=2×10(-5)). In common with two other HLA-B*3501-restricted epitopes, in Gag and Nef, that were not targeted differentially, a response towards NY10 was associated with a significantly lower viral setpoint. Non-immunogenicity of NY10 in B-clade infected subjects derives from the Gag-D260E polymorphism present in ∼90% of B-clade sequences, which critically reduces recognition of the Gag-NY10 epitope. These data suggest that, in spite of any inherent HLA-linked T-cell receptor repertoire differences that may exist, maximizing the breadth of the Gag-specific CD8+ T-cell response, by the addition of even a single epitope, may be of over-riding importance in achieving immune control of HIV infection. This distinction is of direct relevance to development of vaccines designed to optimize the anti-HIV CD8+ T-cell response in all individuals, irrespective of HLA type.

DOI10.1128/JVI.01381-12
Alternate JournalJ. Virol.
PubMed ID22973023