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Nontoxic outer membrane vesicles efficiently increase the efficacy of an influenza vaccine in mice and ferrets

Authors
Shim, Sang-MuSong, Eun-JungSong, DaesubLee, Tae-YoungKim, Doo-JinNam, Jeong-HyunJeong, Dae GwinLee, Chong-KilKim, Sang-HyunKim, Jeong-Ki
Issue Date
27-6월-2017
Publisher
ELSEVIER SCI LTD
Keywords
fmOMV; Adjuvant; Influenza; Pandemic; T cell
Citation
VACCINE, v.35, no.30, pp.3741 - 3748
Indexed
SCIE
SCOPUS
Journal Title
VACCINE
Volume
35
Number
30
Start Page
3741
End Page
3748
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/83089
DOI
10.1016/j.vaccine.2017.05.053
ISSN
0264-410X
Abstract
In this study, we developed a further-modified outer membrane vesicle (fmOMV) from the Delta msbB/Delta pagP mutant of Escherichia coli transformed with the plasmid, pLpxF, in order to use it as an adjuvant for pandemic H1N1 (pH1N1) influenza vaccine. We evaluated the efficacy of the pH1N1 influenza vaccine containing the fmOMV in animal models as compared to the commercial adjuvants, alum or AddaVax(TM). The fmOMV-adjuvanted pH1N1 influenza vaccine induced a significant increase in the humoral immunity; however, this effect was less than that of the AddaVax(Tm). The fmOMV adjuvanted vaccine displayed pronounced an enhanced protective efficacy with increased T cell immune response and reduced the viral load in the lungs of the infected mice after challenging them with a lethal dose of the homologous virus. Moreover, it resulted in a significantly higher cross-protection against heterologous virus challenge than that of the pH1N1 vaccine with alum or with no adjuvants. In ferrets, the fmOMV adjuvanted vaccine elicited a superior antibody response based on the HI titer and efficiently protected the animals from the lethal viral challenges. Taken together, the nontoxic fmOMV could be a promising adjuvant for inducing robust T cell priming into the pH1N1 vaccine and might be broadly applicable to the development of preventive measures against influenza virus infection. (C) 2017 Elsevier Ltd. All rights reserved.
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