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- W2045229650 abstract "We developed the method to efficiently construct recombinant vaccinia viruses based on LC16m8Δ strain that can replicate in mammalian cells but is still safe in human. Immunization in a prime-boost strategy using DNA and LC16m8Δ expressing SIV Gag elicited 7–30-fold more IFN-γ-producing T cells in mice than that using DNA and non-replicating vaccinia DIs recombinant strain. As the previous study on the DNA-prime and recombinant DIs-boost anti-SIV vaccine showed protective efficacy in the macaque model [Someya K, Ami Y, Nakasone T, Izumi Y, Matsuo K, Horibata S, et al. Induction of positive cellular and humoral responses by a prime-boost vaccine encoded with simian immunodeficiency virus gag/pol. J Immunol 2006;176(3):1784–95], LC16m8Δ would have potential as a better recombinant viral vector for HIV vaccine." @default.
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- W2045229650 date "2009-02-01" @default.
- W2045229650 modified "2023-10-14" @default.
- W2045229650 title "Immunogenicity of newly constructed attenuated vaccinia strain LC16m8Δ that expresses SIV Gag protein" @default.
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- W2045229650 doi "https://doi.org/10.1016/j.vaccine.2008.12.015" @default.
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