Identification and specificity of broadly neutralizing antibodies against HIV

被引:173
作者
McCoy, Laura E. [1 ,2 ]
Burton, Dennis R. [1 ,3 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, IAVI Neutralizing Antibody Ctr, Ctr HIV AIDS Vaccine Immunol & Immunogen Discover, La Jolla, CA 92037 USA
[2] UCL, Div Infect & Immun, London, England
[3] Ragon Inst Massachusetts Gen Hosp Massachusetts I, Cambridge, MA USA
关键词
B cells; HIV; monoclonal antibody isolation; neutralization; HUMAN MONOCLONAL-ANTIBODIES; PROXIMAL EXTERNAL REGION; CD4; BINDING-SITE; HIV-1-NEUTRALIZING ANTIBODIES; CONFORMATIONAL EPITOPE; POTENT NEUTRALIZATION; MATURATION PATHWAY; DEPENDENT EPITOPE; STRUCTURAL BASIS; B-CELLS;
D O I
10.1111/imr.12484
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Beginning in 2009, studies of the humoral responses of HIV-positive individuals have led to the identification of scores, if not hundreds, of antibodies that are both broadly reactive and potently neutralizing. This development has provided renewed impetus toward an HIV vaccine and led directly to the development of novel immunogens. Advances in identification of donors with the most potent and broad anti-HIV serum neutralizing responses were crucial in this effort. Equally, development of methods for the rapid generation of human antibodies from these donors was pivotal. Primarily these methods comprise single B-cell culture coupled to high-throughput neutralization screening and flow cytometry-based sorting of single B cells using HIV envelope protein baits. In this review, the advantages and disadvantages of these methodologies are discussed in the context of the specificities targeted by individual antibodies and the need for further improvements to evaluate HIV vaccine candidates.
引用
收藏
页码:11 / 20
页数:10
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