| Literature DB >> 31301135 |
Sushma Boppana1, Sarah Sterrett1, Jacob Files1, Kai Qin1, Andrew Fiore-Gartland2, Kristen W Cohen2, Stephen C De Rosa2, Anju Bansal1, Paul A Goepfert1.
Abstract
HLA-I-associated human immunodeficiency virus (HIV) adaptation is known to negatively affect disease progression and CD8 T-cell responses. We aimed to assess how HLA-I-associated adaptation affects HIV vaccine-induced CD8 T-cell responses in 2 past vaccine efficacy trials. We found that vaccine-encoded adapted epitopes were less immunogenic than vaccine-encoded nonadapted epitopes, and adapted epitope-specific responses were less polyfunctional than nonadapted epitope-specific responses. Along those lines, vaccine recipients with higher HLA-I adaptation to the Gag vaccine insert mounted less polyfunctional CD8 T-cell responses at the protein level. Breadth of response, which correlated with viral control in recipients who became infected, is also dampened by HLA-I adaptation. These findings suggest that HLA-I-associated adaptation is an important consideration for strategies aiming to induce robust CD8 T-cell responses.Entities:
Keywords: HIV-1 vaccine; HIV-specific CD8 T cells; HLA-I; HVTN 502; HVTN 505; adapted epitopes; associated adaptation; polyfunctionality
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Year: 2019 PMID: 31301135 PMCID: PMC6782105 DOI: 10.1093/infdis/jiz368
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226