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Kunjin Virus Replicon Vectors for Human Immunodeficiency Virus Vaccine Development

Sir Albert Sakzewski Virus Research Centre, Royal Children's Hospital,¹ Clinical Medical Virology Centre,² The Australian Centre for International and Tropical Health and Nutrition, Queensland Institute of Medical Research, University of Queensland, Brisbane, Queensland, Australia³

Received 2 December 2002/ Accepted 29 April 2003

We have previously demonstrated the ability of the vaccine vectors based on replicon RNA of the Australian flavivirus Kunjin (KUN) to induce protective antiviral and anticancer CD8⁺ T-cell responses using murine polyepitope as a model immunogen (I. Anraku, T. J. Harvey, R. Linedale, J. Gardner, D. Harrich, A. Suhrbier, and A. A. Khromykh, J. Virol. 76:3791-3799, 2002). Here we showed that immunization of BALB/c mice with KUN replicons encoding HIV-1 Gag antigen resulted in induction of both Gag-specific antibody and protective Gag-specific CD8⁺ T-cell responses. Two immunizations with KUNgag replicons in the form of virus-like particles (VLPs) induced anti-Gag antibodies with titers of ≥1:10,000. Immunization with KUNgag replicons delivered as plasmid DNA, naked RNA, or VLPs induced potent Gag-specific CD8⁺ T-cell responses, with one immunization of KUNgag VLPs inducing 4.5-fold-more CD8⁺ T cells than the number induced after immunization with recombinant vaccinia virus carrying the gag gene (rVVgag). Two immunizations with KUNgag VLPs also provided significant protection against challenge with rVVgag. Importantly, KUN replicon VLP vaccinations induced long-lasting immune responses with CD8⁺ T cells able to secrete gamma interferon and to mediate protection 6 to 10 months after immunization. These results illustrate the potential value of the KUN replicon vectors for human immunodeficiency virus vaccine design.

Publication 148 of the Clinical Medical Virology Centre and the Sir Albert Sakzewski Virus Research Centre, Brisbane, Queensland, Australia.

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