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Background The generation of globally relevant HIV-1 immunogens mimicking native, trimeric Envelope (Env) structure, remains a major challenge for HIV-1 vaccine development. We identified a mosaic Env sequence, originally designed to optimize cellular immunologic coverage of global HIV-1 sequence diversity, which was capable of forming biochemically stable trimers. We assessed this mosaic Env gp140 trimer in guinea pig immunogenicity studies compared to our previously reported biochemically stable C97ZA012 (clade C) trimer. Methods

Stability and neutralization capacity of a novel mosaic HIV-1 gp140 trimer in a guinea pig model