Author:
Andrabi Raiees,Pallesen Jesper,Allen Joel,Song Ge,Zhang Jinsong,de Val Natalia,Gegg Gavin,Porter Katelyn,Su Ching-Yao,Pauthner Matthias,Newman Amanda,Bouton-Vervelle Hilary,Garces Fernando,Wilson Ian A.,Crispin Max,Hahn Beatrice H.,Haynes Barton F.,Verkoczy Laurent,Ward Andrew B.,Burton Dennis R.
Abstract
SummaryEpitope-targeted HIV vaccine design seeks to focus antibody responses to broadly neutralizing antibody (bnAb) sites by sequential immunization. Chimpanzee SIV Envelope (Env) shares a single bnAb site, the V2-apex, with HIV, suggesting its possible utility in an HIV immunization strategy. Accordingly, we generated a chimpanzee SIV Env trimer, MT145K, which displays selective binding to HIV V2-apex bnAbs and precursor versions, but no binding to other HIV specificities. We determined the structure of the MT145K trimer by cryo-EM and showed its architecture was remarkably similar to HIV Env. Immunization of an HIV V2-apex bnAb precursor Ab-expressing knock-in mouse with chimpanzee MT145K trimer induced HIV V2-specific neutralizing responses. Subsequent boosting with an HIV trimer cocktail induced responses exhibiting some virus cross-neutralization. Overall, the chimpanzee MT145K trimer behaves as expected from design both in vitro and in vivo and is an attractive potential component of a sequential immunization regimen to induce V2-apex bnAbs.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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