Immunization expands B cells specific to HIV-1 V3 glycan in mice and macaques

免疫接种可扩增小鼠和猕猴体内针对 HIV-1 V3 聚糖的特异性 B 细胞。

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作者:Amelia Escolano,Harry B Gristick,Morgan E Abernathy,Julia Merkenschlager,Rajeev Gautam,Thiago Y Oliveira,Joy Pai,Anthony P West Jr,Christopher O Barnes,Alexander A Cohen,Haoqing Wang,Jovana Golijanin,Daniel Yost,Jennifer R Keeffe,Zijun Wang,Peng Zhao,Kai-Hui Yao,Jens Bauer,Lilian Nogueira,Han Gao,Alisa V Voll,David C Montefiori,Michael S Seaman,Anna Gazumyan,Murillo Silva,Andrew T McGuire,Leonidas Stamatatos,Darrell J Irvine,Lance Wells,Malcolm A Martin,Pamela J Bjorkman,Michel C Nussenzweig

Abstract

Broadly neutralizing monoclonal antibodies protect against infection with HIV-1 in animal models, suggesting that a vaccine that elicits these antibodies would be protective in humans. However, it has not yet been possible to induce adequate serological responses by vaccination. Here, to activate B cells that express precursors of broadly neutralizing antibodies within polyclonal repertoires, we developed an immunogen, RC1, that facilitates the recognition of the variable loop 3 (V3)-glycan patch on the envelope protein of HIV-1. RC1 conceals non-conserved immunodominant regions by the addition of glycans and/or multimerization on virus-like particles. Immunization of mice, rabbits and rhesus macaques with RC1 elicited serological responses that targeted the V3-glycan patch. Antibody cloning and cryo-electron microscopy structures of antibody-envelope complexes confirmed that immunization with RC1 expands clones of B cells that carry the anti-V3-glycan patch antibodies, which resemble precursors of human broadly neutralizing antibodies. Thus, RC1 may be a suitable priming immunogen for sequential vaccination strategies in the context of polyclonal repertoires.

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