Abstract
BackgroundHeterologous prime-boost immunization protocols using different gene expression systems have proven to be successful tools in protecting against various diseases in experimental animal models. The main reason for using this approach is to exploit the ability of expression cassettes to prime or boost the immune system in different ways during vaccination procedures. The purpose of the project was to study the ability of recombinant vaccinia virus (VV) and bacterial plasmid, both carrying the NS1 gene from tick-borne encephalitis (TBE) virus under the control of different promoters, to protect mice against lethal challenge using a heterologous prime-boost vaccination protocol.ResultsThe heterologous prime-boost vaccination protocol, using a VV recombinant and bacterial plasmid, both containing the NS1 TBE virus protein gene under the control of different promoters, achieved a high level of protection in mice against lethal challenge with a highly pathogenic TBE virus strain. No signs of pronounced TBE infection were detected in the surviving animals.ConclusionHeterologous prime-boost vaccination protocols using recombinant VV and bacterial plasmids could be used for the development of flavivirus vaccines.
Highlights
Heterologous prime-boost immunization protocols using different gene expression systems have proven to be successful tools in protecting against various diseases in experimental animal models
Prime-boost immunization protocols using different expression systems have proven to be successful tools in protecting experimental animals against various important human diseases [1] including tuberculosis [2], AIDS [3], and hepatitis C [4]. The success of such vaccination schemes depends upon the efficiency of the expression systems, of which, recombinant vaccinia virus(VV) and bacterial plasmid vectors are among the more common systems studied [6,7,8]
The recombinant vaccinia virus (W-NS1) in combination with the control plasmid pMV100 protected 20% of challenged mice, whereas 40% of mice survived that were primed with control vaccinia vector VV-WR and boosted with the NS1 gene expressing plasmid pMV45
Summary
Heterologous prime-boost immunization protocols using different gene expression systems have proven to be successful tools in protecting against various diseases in experimental animal models. Prime-boost immunization protocols using different expression systems have proven to be successful tools in protecting experimental animals against various important human diseases [1] including tuberculosis [2], AIDS [3], and hepatitis C [4]. The success of such vaccination schemes depends upon the efficiency of the expression systems, of which, recombinant vaccinia virus(VV) and bacterial plasmid vectors are among the more common systems studied [6,7,8]. It has been shown that when at least one component in a prime-boost vaccination scheme includes a plasmid vector, there is a strong (page number not for citation purposes)
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