| Literature DB >> 27192579 |
Daniel T MacLeod1, Nancy M Choi1, Bryan Briney2, Fernando Garces3, Lorena S Ver1, Elise Landais1, Ben Murrell4, Terri Wrin5, William Kilembe6, Chi-Hui Liang7, Alejandra Ramos1, Chaoran B Bian1, Lalinda Wickramasinghe1, Leopold Kong3, Kemal Eren4, Chung-Yi Wu8, Chi-Huey Wong8, Sergei L Kosakovsky Pond4, Ian A Wilson3, Dennis R Burton9, Pascal Poignard10.
Abstract
The high-mannose patch on HIV Env is a preferred target for broadly neutralizing antibodies (bnAbs), but to date, no vaccination regimen has elicited bnAbs against this region. Here, we present the development of a bnAb lineage targeting the high-mannose patch in an HIV-1 subtype-C-infected donor from sub-Saharan Africa. The Abs first acquired autologous neutralization, then gradually matured to achieve breadth. One Ab neutralized >47% of HIV-1 strains with only ∼11% somatic hypermutation and no insertions or deletions. By sequencing autologous env, we determined key residues that triggered the lineage and participated in Ab-Env coevolution. Next-generation sequencing of the Ab repertoire showed an early expansive diversification of the lineage followed by independent maturation of individual limbs, several of them developing notable breadth and potency. Overall, the findings are encouraging from a vaccine standpoint and suggest immunization strategies mimicking the evolution of the entire high-mannose patch and promoting maturation of multiple diverse Ab pathways.Entities:
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Year: 2016 PMID: 27192579 PMCID: PMC5003182 DOI: 10.1016/j.immuni.2016.04.016
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745