| Literature DB >> 29132197 |
Hanseul Oh1, C-Yoon Kim2, Chang-Hwan Kim3, Gyeung-Haeng Hur3, Ji Min Lee1, Seo-Na Chang1, Jae-Hak Park1.
Abstract
Francisella tularensis (FT), a highly infectious pathogen, is considered to be a potential biological weapon owing to the current lack of a human vaccine against it. Tul4 and FopA, both outer membrane proteins of FT, play an important role in the bacterium's immunogenicity. In the present study, we evaluated the immune response of mice-humanized with human CD34+ cells (hu-mice)-to a cocktail of recombinant Tul4 and FopA (rTul4 and rFopA), which were codon-optimized and expressed in Escherichia coli. Not only did the cocktail-immunized hu-mice produce a significant human immunoglobulin response, they also exhibited prolonged survival against an attenuated live vaccine strain as well as human T cells in the spleen. These results suggest that the cocktail of rTul4 and rFopA had successfully induced an immune response in the hu-mice, demonstrating the potential of this mouse model for use in the evaluation of FT vaccine candidates.Entities:
Keywords: Francisella tularensis; humanized mice; vaccine
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Year: 2018 PMID: 29132197 DOI: 10.4014/jmb.1707.07075
Source DB: PubMed Journal: J Microbiol Biotechnol ISSN: 1017-7825 Impact factor: 2.351