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About:
Single intranasal immunization with chimpanzee adenovirus-based vaccine induces sustained and protective immunity against MERS-CoV infection
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Single intranasal immunization with chimpanzee adenovirus-based vaccine induces sustained and protective immunity against MERS-CoV infection
Creator
Zhang, Chao
Zhao, Jincun
Jia, Wenxu
Shi, Xuanling
Wang, Xinquan
Zhang, Linqi
Zhou, Panpan
Perlman, Stanley
Channappanavar, Rudragouda
Zhou, Dongming
Li, Mingxi
Shan, Sisi
Xu, Jiuyang
Zhang, Shuyuan
Zhou, Haixia
topic
covid:89c52fc69362dbc2c29ed79aa72928ad14dc4c80#this
source
Medline; PMC
abstract
The recently identified Middle East Respiratory Syndrome Coronavirus (MERS-CoV) causes severe and fatal acute respiratory illness in humans. However, no approved prophylactic and therapeutic interventions are currently available. The MERS-CoV envelope spike protein serves as a crucial target for neutralizing antibodies and vaccine development, as it plays a critical role in mediating viral entry through interactions with the cellular receptor, dipeptidyl peptidase 4 (DPP4). Here, we constructed a recombinant rare serotype of the chimpanzee adenovirus 68 (AdC68) that expresses full-length MERS-CoV S protein (AdC68-S). Single intranasal immunization with AdC68-S induced robust and sustained neutralizing antibody and T cell responses in BALB/c mice. In a human DPP4 knock-in (hDPP4-KI) mouse model, it completely protected against lethal challenge with a mouse-adapted MERS-CoV (MERS-CoV-MA). Passive transfer of immune sera to naïve hDPP4-KI mice also provided survival advantages from lethal MERS-CoV-MA challenge. Analysis of sera absorption and isolated monoclonal antibodies from immunized mice demonstrated that the potent and broad neutralizing activity was largely attributed to antibodies targeting the receptor binding domain (RBD) of the S protein. These results show that AdC68-S can induce protective immune responses in mice and represent a promising candidate for further development against MERS-CoV infection in both dromedaries and humans.
has issue date
2019-05-25
(
xsd:dateTime
)
bibo:doi
10.1080/22221751.2019.1620083
bibo:pmid
31130102
has license
cc-by
sha1sum (hex)
89c52fc69362dbc2c29ed79aa72928ad14dc4c80
schema:url
https://doi.org/10.1080/22221751.2019.1620083
resource representing a document's title
Single intranasal immunization with chimpanzee adenovirus-based vaccine induces sustained and protective immunity against MERS-CoV infection
has PubMed Central identifier
PMC6542157
has PubMed identifier
31130102
schema:publication
Emerg Microbes Infect
resource representing a document's body
covid:89c52fc69362dbc2c29ed79aa72928ad14dc4c80#body_text
is
http://vocab.deri.ie/void#inDataset
of
https://covidontheweb.inria.fr:4443/about/id/http/ns.inria.fr/covid19/89c52fc69362dbc2c29ed79aa72928ad14dc4c80
is
schema:about
of
named entity 'constructed'
named entity 'fatal'
named entity 'transfer'
named entity 'humans'
named entity 'human'
named entity 'antibodies'
named entity 'robust'
named entity 'absorption'
named entity 'survival'
named entity 'induces'
covid:arg/89c52fc69362dbc2c29ed79aa72928ad14dc4c80
named entity 'binding domain'
named entity 'humans'
named entity 'respiratory illness'
named entity 'prophylactic'
named entity 'promising'
named entity 'MERS-CoV'
named entity 'induced'
named entity 'sera'
named entity 'rare'
named entity 'mediating'
named entity 'MERS-CoV'
named entity 'knock-in'
named entity 'mice'
named entity 'respiratory illness'
named entity 'antibodies'
named entity 'mouse model'
named entity 'immune responses'
named entity 'cellular receptor'
named entity 'DPP4'
named entity 'intranasal'
named entity 'recombinant'
named entity 'DPP4'
named entity 'MERS-CoV'
named entity 'vaccine'
named entity 'Passive transfer'
named entity 'MERS-CoV'
named entity 'immunization'
named entity 'chimpanzee'
named entity 'vaccine'
named entity 'MERS-CoV'
named entity 'RBD'
named entity 'MERS-CoV'
named entity 'dromedaries'
named entity 'IgG1'
named entity 'serum'
named entity 'protein'
named entity 'Carlsbad, CA'
named entity 'human infection'
named entity 'vaccine'
named entity 'infection'
named entity 'MERS-CoV'
named entity 'RBD'
named entity 'viruses'
named entity 'monoclonal antibodies'
named entity 'molecular weight'
named entity 'serum'
named entity 'antibodies'
named entity 'antibody'
named entity 'MERS'
named entity 'MERS-CoV'
named entity 'monoclonal antibodies'
named entity 'IgG'
named entity 'Ebola virus'
named entity 'protein'
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