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About:
Immunoglobulin fragment F(ab’)(2) against RBD potently neutralizes SARS-CoV-2 in vitro
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
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
has title
Immunoglobulin fragment F(ab’)(2) against RBD potently neutralizes SARS-CoV-2 in vitro
Creator
Chen, R
Sun, J
Xiao, Z
Zhang, Y
Zhao, Y
Shi, J
Wu, T
Zhou, X
Fang, W
Shi, X
Fan, P
Gong, S
Jiang, L
Research Pan, Antiviral
Shang, X
topic
covid:18c7340382aefdae419f2dbe5dbb04df6215a7c4#this
Source
Elsevier; Medline; PMC
abstract
COVID-19, which is caused by the emerging human coronavirus SARS-CoV-2, has become a global pandemic that poses a serious threat to human health. To date, no vaccines or specific antiviral drugs have been approved for the treatment of this disease in clinic. Herein, therapeutic antibodies for SARS-CoV-2 were obtained from hyperimmune equine plasma. First, a recombinant SARS-CoV-2 spike protein receptor-binding domain (RBD) was obtained in gram-level quantities through high-cell density fermentation of Chinese hamster ovary cells. Then, the binding of the RBD to the SARS-CoV-2 receptor, human angiotensin-converting enzyme 2, was verified by several biochemical methods. The efficacy of the RBD in triggering antibody response in vivo was subsequently tested in both mice and equines, and the results showed that the RBD triggered high-titer neutralizing antibody production in vivo. Immunoglobulin F(ab’)(2) fragments were prepared from equine antisera via removal of the Fc region from the immunoglobulins. Finally, a neutralization test with live virus demonstrated that RBD-specific F(ab’)(2) inhibited SARS-CoV-2 with an EC(50) of 0.07 μg/ml and an EC(80) of 0.18 μg/ml, showing a potent inhibitory effect on SARS-CoV-2. These results highlight RBD-specific equine immunoglobulin F(ab’)(2) fragment as a candidate for the treatment of SARS-CoV-2.
has issue date
2020-07-10
(
xsd:dateTime
)
bibo:doi
10.1016/j.antiviral.2020.104868
bibo:pmid
32659292
has license
no-cc
sha1sum (hex)
18c7340382aefdae419f2dbe5dbb04df6215a7c4
schema:url
https://doi.org/10.1016/j.antiviral.2020.104868
resource representing a document's title
Immunoglobulin fragment F(ab’)(2) against RBD potently neutralizes SARS-CoV-2 in vitro
has PubMed Central identifier
PMC7351055
has PubMed identifier
32659292
schema:publication
Antiviral Res
resource representing a document's body
covid:18c7340382aefdae419f2dbe5dbb04df6215a7c4#body_text
is
http://vocab.deri.ie/void#inDataset
of
proxy:http/ns.inria.fr/covid19/18c7340382aefdae419f2dbe5dbb04df6215a7c4
is
schema:about
of
named entity 'Fc region'
named entity 'inhibited'
named entity 'poses'
named entity 'RBD'
named entity 'Immunoglobulin'
named entity 'inhibitory'
named entity 'QUANTITIES'
named entity 'REMOVAL'
named entity 'FRAGMENTS'
named entity 'PREPARED'
named entity '0.07'
named entity 'CANDIDATE'
named entity 'EQUINE'
named entity 'HIGH'
named entity 'IN VIVO'
named entity 'DATE'
named entity 'candidate'
named entity 'production'
named entity 'antibodies'
named entity 'emerging'
named entity 'response'
named entity 'prepared'
named entity 'caused'
named entity 'removal'
named entity 'vaccines'
named entity 'antibody'
named entity 'fermentation'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'mice'
named entity 'virus'
named entity 'Immunoglobulin'
named entity 'SARS-CoV-2'
named entity 'RBD'
named entity 'RBD'
named entity 'plasma'
named entity 'RBD'
named entity 'biochemical'
named entity 'immunoglobulin'
named entity 'RBD'
named entity 'RBD'
named entity 'triggered'
named entity 'assay'
named entity '3,3',5,5'-tetramethylbenzidine'
named entity 'Laboratory Animal'
named entity 'Fc regions'
named entity 'SARS-CoV-2'
named entity 'protein'
named entity 'protein'
named entity 'thrombin'
named entity 'immunizations'
named entity 'Dulbecco's modified Eagle's medium'
named entity 'antigenicity'
named entity 'RBD'
named entity 'Chinese Academy of Sciences'
named entity 'antibody response'
named entity 'murine'
named entity 'intramuscular injection'
named entity 'antibody response'
named entity 'plasma collection'
named entity 'immunoglobulins'
named entity 'Chinese Academy of Sciences'
named entity 'rhesus monkeys'
named entity 'PBS'
named entity 'virus'
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