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About:
A Novel Bacterium-Like Particle-Based Vaccine Displaying the SUDV Glycoprotein Induces Potent Humoral and Cellular Immune Responses in Mice
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
A Novel Bacterium-Like Particle-Based Vaccine Displaying the SUDV Glycoprotein Induces Potent Humoral and Cellular Immune Responses in Mice
Creator
Xia, Xianzhu
Yang, Songtao
He, Hongbin
Wang, Jianzhong
Chi, Hang
Feng, Na
Gao, Yuwei
Wang, Hualei
Zhao, Yongkun
Zhang, Shengnan
Jin, Hongli
Li, Entao
Yan, Feihu
Cao, Zengguo
Jiao, Cuicui
Li, Wujian
Shi, Zhikang
Xu, Shengnan
Source
Medline; PMC
abstract
Sudan virus (SUDV) causes severe lethal hemorrhagic fever in humans and nonhuman primates. The most effective and economical way to protect against Sudan ebolavirus disease is prophylactic vaccination. However, there are no licensed vaccines to prevent SUDV infections. In this study, a bacterium-like particle (BLP)-based vaccine displaying the extracellular domain of the SUDV glycoprotein (eGP) was developed based on a gram-positive enhancer matrix-protein anchor (GEM-PA) surface display system. Expression of the recombinant GEM-displayed eGP (eGP-PA-GEM) was verified by Western blotting and immunofluorescence assays. The SUDV BLPs (SBLPs), which were mixed with Montanide ISA 201VG plus Poly (I:C) combined adjuvant, could induce high SUDV GP-specific IgG titers of up to 1:40,960 and robust virus-neutralizing antibody titers reached 1:460. The SBLP also elicited T-helper 1 (Th1) and T-helper 2 (Th2) cell-mediated immunity. These data indicate that the SBLP subunit vaccine has the potential to be developed into a promising candidate vaccine against SUDV infections.
has issue date
2019-12-11
(
xsd:dateTime
)
bibo:doi
10.3390/v11121149
bibo:pmid
31835785
has license
cc-by
sha1sum (hex)
4bcdac71c12d45032dfb8c6753e7d94643a11283
schema:url
https://doi.org/10.3390/v11121149
resource representing a document's title
A Novel Bacterium-Like Particle-Based Vaccine Displaying the SUDV Glycoprotein Induces Potent Humoral and Cellular Immune Responses in Mice
has PubMed Central identifier
PMC6950126
has PubMed identifier
31835785
schema:publication
Viruses
resource representing a document's body
covid:4bcdac71c12d45032dfb8c6753e7d94643a11283#body_text
is
schema:about
of
named entity 'immunofluorescence assays'
named entity 'prevent'
named entity 'EVD'
named entity 'outbreak'
named entity 'vaccine'
named entity 'surface'
named entity 'The'
named entity 'EBOV'
named entity 'Immune'
covid:arg/4bcdac71c12d45032dfb8c6753e7d94643a11283
named entity 'cases'
named entity 'study'
named entity 'These'
named entity 'IgG'
named entity 'EVD'
named entity 'infections'
named entity 'Bundibugyo'
named entity 'Th2'
named entity '1998'
named entity 'antibody'
named entity 'receiving'
named entity 'vaccination'
named entity 'adjuvant'
named entity 'Taï Forest'
named entity 'T-helper'
named entity 'reached'
named entity 'subunit vaccine'
named entity '2018'
named entity 'enhancer'
named entity 'Sudan ebolavirus'
named entity 'subunit vaccine'
named entity 'ebolaviruses'
named entity 'recombinant'
named entity 'SUDV'
named entity 'EVD'
named entity 'SUDV'
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named entity 'SUDV'
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named entity 'IgG'
named entity 'virus-like particle'
named entity 'IL-4'
named entity 'neutralizing antibody'
named entity 'germinal center'
named entity 'TNF-α'
named entity 'protein expression'
named entity 'Th2 response'
named entity 'SUDV'
named entity 'IgG2a'
named entity 'morbidity'
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named entity 'La Jolla'
named entity 'Stockholm'
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named entity 'antigens'
named entity 'SUDV'
named entity 'one-way ANOVA'
named entity 'TNF-α'
named entity 'antibody'
named entity 'IL-10'
named entity 'T-helper'
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