Elicitation of HIV-1-neutralizing antibodies against the CD4-binding site

被引:30
作者
Georgiev, Ivelin S. [1 ]
Joyce, M. Gordon [1 ]
Zhou, Tongqing [1 ]
Kwong, Peter D. [1 ]
机构
[1] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
antibody template; B-cell ontogeny; gp120 envelope glycoprotein; HIV-1; vaccine; structure-based design; HIV-1 ENVELOPE GLYCOPROTEINS; B-CELL RESPONSES; CD4; BINDING-SITE; STRUCTURAL BASIS; NEUTRALIZING ANTIBODY; ENV TRIMERS; MONOCLONAL-ANTIBODIES; IMMUNOGEN DESIGN; OUTER DOMAIN; GENE USAGE;
D O I
10.1097/COH.0b013e328363a90e
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of reviewThe HIV-1 site of binding for the CD4 receptor has long attracted attention as a potential supersite of vulnerability to antibody-mediated neutralization. We review recent findings related to effective CD4-binding site antibodies isolated from HIV-1-infected individuals and discuss implications for immunogen design.Recent findingsHighly effective CD4-binding site antibodies such as antibody VRC01 have the ability to neutralize over 90% of circulating HIV-1 strains. Sequence and structural analysis of these antibodies from over half a dozen HIV-1-infected donors reveals remarkable similarity in their ontogenies and their modes of recognition, all of which involve mimicry of CD4 receptor by antibody-heavy chain. Meanwhile, other effective CD4-binding site neutralizers such as antibody CH103 have been shown to utilize a different mode of recognition, with next-generation sequencing of both virus and antibody suggesting co-evolution to drive the development of antibody-neutralization breadth.SummaryThe nexus of information concerning the CD4-binding site and its recognition by human antibodies capable of effective neutralization has expanded remarkably in the last few years. Although barriers are substantial, new insights from donor-serum responses, atomic-level structures of antibody-Env complexes, and next-generation sequencing of B-cell transcripts are invigorating vaccine-design efforts to elicit effective CD4-binding site antibodies.
引用
收藏
页码:382 / 392
页数:11
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