| Literature DB >> 26180102 |
Heather A Prentice1, Georgia D Tomaras2, Daniel E Geraghty3, Richard Apps4, Youyi Fong5, Philip K Ehrenberg6, Morgane Rolland1, Gustavo H Kijak1, Shelly J Krebs1, Wyatt Nelson3, Allan DeCamp5, Xiaoying Shen2, Nicole L Yates2, Susan Zolla-Pazner7, Sorachai Nitayaphan8, Supachai Rerks-Ngarm9, Jaranit Kaewkungwal10, Punnee Pitisuttithum11, Guido Ferrari2, M Juliana McElrath5, David C Montefiori2, Robert T Bailer12, Richard A Koup12, Robert J O'Connell8, Merlin L Robb1, Nelson L Michael6, Peter B Gilbert5, Jerome H Kim6, Rasmi Thomas13.
Abstract
In the RV144 vaccine trial, two antibody responses were found to correlate with HIV-1 acquisition. Because human leukocyte antigen (HLA) class II-restricted CD4(+) T cells are involved in antibody production, we tested whether HLA class II genotypes affected HIV-1-specific antibody levels and HIV-1 acquisition in 760 individuals. Indeed, antibody responses correlated with acquisition only in the presence of single host HLA alleles. Envelope (Env)-specific immunoglobulin A (IgA) antibodies were associated with increased risk of acquisition specifically in individuals with DQB1*06. IgG antibody responses to Env amino acid positions 120 to 204 were higher and were associated with decreased risk of acquisition and increased vaccine efficacy only in the presence of DPB1*13. Screening IgG responses to overlapping peptides spanning Env 120-204 and viral sequence analysis of infected individuals defined differences in vaccine response that were associated with the presence of DPB1*13 and could be responsible for the protection observed. Overall, the underlying genetic findings indicate that HLA class II modulated the quantity, quality, and efficacy of antibody responses in the RV144 trial.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26180102 PMCID: PMC4911012 DOI: 10.1126/scitranslmed.aab4005
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956