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Receptor-binding domain-based subunit vaccines against MERS-CoV
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PubMed
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Europe PubMed Central
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13 July 2022
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PubMed
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22 October 2022
title
Receptor-binding domain-based subunit vaccines against MERS-CoV
(English)
1 reference
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PubMed
main subject
Middle East respiratory syndrome coronavirus
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author
Lu Lu
object named as
Lu Lu
series ordinal
3
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Shibo Jiang
series ordinal
4
object named as
Shibo Jiang
1 reference
stated in
Crossref
Lanying Du
series ordinal
5
object named as
Lanying Du
1 reference
stated in
Crossref
Naru Zhang
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1
object named as
Naru Zhang
1 reference
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author name string
Jian Tang
series ordinal
2
1 reference
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language of work or name
English
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PubMed
publication date
16 April 2015
3 references
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PubMed
stated in
PubMed Central
retrieved
13 July 2022
stated in
PubMed Central
retrieved
22 October 2022
published in
Virus Research
3 references
stated in
PubMed
stated in
PubMed Central
retrieved
13 July 2022
stated in
PubMed Central
retrieved
22 October 2022
volume
202
1 reference
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PubMed
page(s)
151-9
1 reference
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PubMed
cites work
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Crystal Structure of the Receptor-Binding Domain from Newly Emerged Middle East Respiratory Syndrome Coronavirus
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A highly conserved WDYPKCDRA epitope in the RNA directed RNA polymerase of human coronaviruses can be used as epitope-based universal vaccine design
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A conformation-dependent neutralizing monoclonal antibody specifically targeting receptor-binding domain in Middle East respiratory syndrome coronavirus spike protein.
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Intranasal vaccination with recombinant receptor-binding domain of MERS-CoV spike protein induces much stronger local mucosal immune responses than subcutaneous immunization: Implication for designing novel mucosal MERS vaccines.
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Yeast-expressed recombinant protein of the receptor-binding domain in SARS-CoV spike protein with deglycosylated forms as a SARS vaccine candidate
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A truncated receptor-binding domain of MERS-CoV spike protein potently inhibits MERS-CoV infection and induces strong neutralizing antibody responses: implication for developing therapeutics and vaccines
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Evaluation of serologic and antigenic relationships between middle eastern respiratory syndrome coronavirus and other coronaviruses to develop vaccine platforms for the rapid response to emerging coronaviruses
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Wild-type and innate immune-deficient mice are not susceptible to the Middle East respiratory syndrome coronavirus
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Middle East respiratory syndrome coronavirus (MERS-CoV) causes transient lower respiratory tract infection in rhesus macaques
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28 November 2018
Lack of small animal model hinders MERS coronavirus research.
1 reference
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4439384
retrieved
28 November 2018
Antibodies induced by receptor-binding domain in spike protein of SARS-CoV do not cross-neutralize the novel human coronavirus hCoV-EMC.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4439384
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28 November 2018
A predicted receptor-binding and critical neutralizing domain in S protein of the novel human coronavirus HCoV-EMC.
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PubMed Central
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28 November 2018
Cross-neutralization of human and palm civet severe acute respiratory syndrome coronaviruses by antibodies targeting the receptor-binding domain of spike protein.
1 reference
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Evidence for camel-to-human transmission of MERS coronavirus
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7 January 2021
Receptor-binding domain of SARS-CoV spike protein induces long-term protective immunity in an animal model
1 reference
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Crossref
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7 January 2021
Identification of a critical neutralization determinant of severe acute respiratory syndrome (SARS)-associated coronavirus: importance for designing SARS vaccines
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Crossref
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retrieved
7 January 2021
Identifiers
DOI
10.1016/J.VIRUSRES.2014.11.013
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2889525
OpenCitations bibliographic resource ID
2889525
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2889525
PMC publication ID
4439384
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2889525
PubMed publication ID
25445336
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2889525
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