Authors
Sandrine L Hulot, Bette Korber, Elena E Giorgi, Nathan Vandergrift, Kevin O Saunders, Harikrishnan Balachandran, Linh V Mach, Michelle A Lifton, Giuseppe Pantaleo, Jim Tartaglia, Sanjay Phogat, Bertram Jacobs, Karen Kibler, Beatriz Perdiguero, Carmen E Gomez, Mariano Esteban, Margherita Rosati, Barbara K Felber, George N Pavlakis, Robert Parks, Krissey Lloyd, Laura Sutherland, Richard Scearce, Norman L Letvin, Michael S Seaman, S Munir Alam, David Montefiori, Hua-Xin Liao, Barton F Haynes, Sampa Santra
Publication date
2015/6/15
Journal
Journal of virology
Volume
89
Issue
12
Pages
6462-6480
Publisher
American Society for Microbiology
Description
An effective human immunodeficiency virus type 1 (HIV-1) vaccine must induce protective antibody responses, as well as CD4+ and CD8+ T cell responses, that can be effective despite extraordinary diversity of HIV-1. The consensus and mosaic immunogens are complete but artificial proteins, computationally designed to elicit immune responses with improved cross-reactive breadth, to attempt to overcome the challenge of global HIV diversity. In this study, we have compared the immunogenicity of a transmitted-founder (T/F) B clade Env (B.1059), a global group M consensus Env (Con-S), and a global trivalent mosaic Env protein in rhesus macaques. These antigens were delivered using a DNA prime-recombinant NYVAC (rNYVAC) vector and Env protein boost vaccination strategy. While Con-S Env was a single sequence, mosaic immunogens were a set of three Envs optimized to include the most common …
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