Immunofocusing and enhancing autologous Tier-2 HIV-1 neutralization by displaying Env trimers on two-component protein nanoparticles

Brouwer, Philip J. M.; Antanasijevic, Aleksandar; de Gast, Marlon; Allen, Joel D.; Bijl, Tom P. L.; Yasmeen, Anila; Ravichandran, Rashmi; Burger, Judith A.; Ozorowski, Gabriel; Torres, Jonathan L.; LaBranche, Celia; Montefiori, David C.; Ringe, Rajesh P.; van Gils, Marit J.; Moore, John P.; Klasse, Per Johan; Crispin, Max; King, Neil P.; Ward, Andrew B.; Sanders, Rogier W.

The HIV-1 envelope glycoprotein trimer is poorly immunogenic because it is covered by a dense glycan shield. As a result, recombinant Env glycoproteins generally elicit inadequate antibody levels that neutralize clinically-relevant, neutralization-resistant (Tier-2) HIV-1 strains. Multivalent antigen presentation on nanoparticles is an established strategy to increase vaccine-driven immune responses. However, due to nanoparticle instability in vivo, the display of non-native Env structures, and the inaccessibility of many neutralizing antibody (NAb) epitopes, the effects of nanoparticle display have been modest for Env trimers. Here, we generated two-component self-assembling protein nanoparticles presenting twenty SOSIP trimers of the clade C Tier-2 genotype 16055. An immunization study in rabbits demonstrated that these nanoparticles induced 60-fold higher autologous Tier-2 NAb titers than the corresponding SOSIP trimers. Epitope mapping revealed that nanoparticle presentation focused antibody responses to an immunodominant apical epitope. Thus, these nanoparticles are a promising platform to improve the immunogenicity of Env trimers with apex-proximate NAb epitopes.