| Literature DB >> 27806295 |
Christina Yacoob1, Marie Pancera2, Vladimir Vigdorovich3, Brian G Oliver3, Jolene A Glenn1, Junli Feng1, D Noah Sather3, Andrew T McGuire1, Leonidas Stamatatos4.
Abstract
Elicitation of broadly neutralizing antibodies remains a long-standing goal of HIV vaccine research. Although such antibodies can arise during HIV-1 infection, gaps in our knowledge of their germline, pre-immune precursor forms, as well as on their interaction with viral Env, limit our ability to elicit them through vaccination. Studies of broadly neutralizing antibodies from the VRC01-class provide insight into progenitor B cell receptors (BCRs) that could develop into this class of antibodies. Here, we employed high-throughput heavy chain variable region (VH)/light chain variable region (VL) deep sequencing, combined with biophysical, structural, and modeling antibody analyses, to interrogate circulating potential VRC01-progenitor BCRs in healthy individuals. Our study reveals that not all humans are equally predisposed to generate VRC01-class antibodies, not all predicted progenitor VRC01-expressing B cells can bind to Env, and the CDRH3 region of germline VRC01 antibodies influence their ability to recognize HIV-1. These findings will be critical to the design of optimized immunogens that should consider CDRH3 interactions.Entities:
Keywords: CDRH3; HIV; VRC01; broadly neutralizing antibodies; germline; human alleles; human antibodies
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Year: 2016 PMID: 27806295 PMCID: PMC5207042 DOI: 10.1016/j.celrep.2016.10.017
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423