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Tracing HIV-1 strains that imprint broadly neutralizing antibody responses

Authors :
Kouyos, Roger D.
Rusert, Peter
Kadelka, Claus
Huber, Michael
Marzel, Alex
Ebner, Hanna
Schanz, Merle
Liechti, Thomas
Friedrich, Nikolas
Braun, Dominique L.
Scherrer, Alexandra U.
Weber, Jacqueline
Uhr, Therese
Baumann, Nicolas S.
Leemann, Christine
Kuster, Herbert
Chave, Jean-Philippe
Cavassini, Matthias
Bernasconi, Enos
Hoffmann, Matthias
Calmy, Alexandra
Battegay, Manuel
Rauch, Andri
Yerly, Sabine
Aubert, Vincent
Klimkait, Thomas
Böni, Jürg
Metzner, Karin J.
Günthard, Huldrych F.
Trkola, Alexandra
Source :
Nature; September 2018, Vol. 561 Issue: 7723 p406-410, 5p
Publication Year :
2018

Abstract

Understanding the determinants of broadly neutralizing antibody (bNAb) evolution is crucial for the development of bNAb-based HIV vaccines1. Despite emerging information on cofactors that promote bNAb evolution in natural HIV-1 infections, in which the induction of bNAbs is genuinely rare2, information on the impact of the infecting virus strain on determining the breadth and specificity of the antibody responses to HIV-1 is lacking. Here we analyse the influence of viral antigens in shaping antibody responses in humans. We call the ability of a virus strain to induce similar antibody responses across different hosts its antibody-imprinting capacity, which from an evolutionary biology perspective corresponds to the viral heritability of the antibody responses. Analysis of 53 measured parameters of HIV-1-binding and neutralizing antibody responses in a cohort of 303 HIV-1 transmission pairs (individuals who harboured highly related HIV-1 strains and were putative direct transmission partners or members of an HIV-1 transmission chain) revealed that the effect of the infecting virus on the outcome of the bNAb response is moderate in magnitude but highly significant. We introduce the concept of bNAb-imprinting viruses and provide evidence for the existence of such viruses in a systematic screening of our cohort. The bNAb-imprinting capacity can be substantial, as indicated by a transmission pair with highly similar HIV-1 antibody responses and strong bNAb activity. Identification of viruses that have bNAb-imprinting capacities and their characterization may thus provide the potential to develop lead immunogens.

Details

Language :
English
ISSN :
00280836 and 14764687
Volume :
561
Issue :
7723
Database :
Supplemental Index
Journal :
Nature
Publication Type :
Periodical
Accession number :
ejs50964745
Full Text :
https://doi.org/10.1038/s41586-018-0517-0