Chimpanzee SIV Envelope trimer: structure and deployment as an HIV vaccine template
R. Andrabi, J. Pallesen, J. Allen, G. Song, J. Zhang, N. de Val, G. Gegg, K. Porter, C.-Y. Su, M. Pauthner, A. Newman, H. Bouton-Vervelle, F. Garces, I. A. Wilson, M. Crispin, B. H. Hahn, B. F. Haynes, L. Verkoczy, A. B. Ward, D. R. Burton
Abstract
Epitope-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.
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