| Literature DB >> 25865483 |
Xueling Wu1, Zhenhai Zhang2, Chaim A Schramm3, M Gordon Joyce4, Young Do Kwon4, Tongqing Zhou4, Zizhang Sheng3, Baoshan Zhang4, Sijy O'Dell4, Krisha McKee4, Ivelin S Georgiev4, Gwo-Yu Chuang4, Nancy S Longo4, Rebecca M Lynch4, Kevin O Saunders4, Cinque Soto4, Sanjay Srivatsan4, Yongping Yang4, Robert T Bailer4, Mark K Louder4, James C Mullikin5, Mark Connors6, Peter D Kwong7, John R Mascola8, Lawrence Shapiro9.
Abstract
HIV-1-neutralizing antibodies develop in most HIV-1-infected individuals, although highly effective antibodies are generally observed only after years of chronic infection. Here, we characterize the rate of maturation and extent of diversity for the lineage that produced the broadly neutralizing antibody VRC01 through longitudinal sampling of peripheral B cell transcripts over 15 years and co-crystal structures of lineage members. Next-generation sequencing identified VRC01-lineage transcripts, which encompassed diverse antibodies organized into distinct phylogenetic clades. Prevalent clades maintained characteristic features of antigen recognition, though each evolved binding loops and disulfides that formed distinct recognition surfaces. Over the course of the study period, VRC01-lineage clades showed continuous evolution, with rates of ∼2 substitutions per 100 nucleotides per year, comparable to that of HIV-1 evolution. This high rate of antibody evolution provides a mechanism by which antibody lineages can achieve extraordinary diversity and, over years of chronic infection, develop effective HIV-1 neutralization.Entities:
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Year: 2015 PMID: 25865483 PMCID: PMC4706178 DOI: 10.1016/j.cell.2015.03.004
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582