Development of a synthetic consensus sequence scrambled antigen HIV-1 vaccine designed for global use

Scott A. Thomson*, Angel B. Jaramillo, Maryanne Shoobridge, Kerrie J. Dunstan, Beth Everett, Charani Ranasinghe, Stephen J. Kent, Ke Gao, Jill Medveckzy, Rosemary A. Ffrench, Ian A. Ramshaw

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    33 Citations (Scopus)

    Abstract

    Induction of high levels of broadly reactive cytotoxic T lymphocytes (CTL) remains a promising approach for an effective HIV-1 vaccine. We have developed a novel genetic-based vaccine strategy that encodes consensus overlapping peptide sets from all HIV-1 proteins scrambled together. This synthetic scrambled antigen vaccine (SAVINE) strategy has significant advantages, e.g. capacity to encode more antigens safely and is very flexible compared to traditional isolate-based strategies. The SAVINE vaccine strategy is clearly immunogenic, being able to restimulate a range of human HIV-1 specific responses in vitro and induce HIV-1 specific immunity in vivo in mice. Interestingly, different in vivo delivery strategies affected the resulting immunity and immunodominance pattern in mice. This platform strategy could be used for other infections and cancers where T cell responses are important for protection.

    Original languageEnglish
    Pages (from-to)4647-4657
    Number of pages11
    JournalVaccine
    Volume23
    Issue number38
    DOIs
    Publication statusPublished - 7 Sept 2005

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