Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus.
Identifieur interne : 000E68 ( Ncbi/Merge ); précédent : 000E67; suivant : 000E69Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus.
Auteurs : Jincun Zhao [République populaire de Chine] ; Wei Wang ; Guang-Fa Wang ; Yonghua Li ; Hui Zhuang ; Xiaoyuan Xu ; Furong Ren ; Zhendong Zhao ; Xiao-Ming GaoSource :
- Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology [ 1386-6532 ] ; 2005.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Anticorps antiviraux (sang), Femelle, Glycoprotéine de spicule des coronavirus, Glycoprotéines membranaires (génétique), Glycoprotéines membranaires (immunologie), Humains, Immunoglobuline G (sang), Mâle, Protéines de l'enveloppe virale (génétique), Protéines de l'enveloppe virale (immunologie), Protéines recombinantes (génétique), Protéines recombinantes (immunologie), Sensibilité et spécificité, Syndrome respiratoire aigu sévère, Test ELISA, Virus du SRAS.
- MESH :
- génétique : Glycoprotéines membranaires, Protéines de l'enveloppe virale, Protéines recombinantes.
- immunologie : Glycoprotéines membranaires, Protéines de l'enveloppe virale, Protéines recombinantes.
- sang : Anticorps antiviraux, Immunoglobuline G.
- Adolescent, Adulte, Adulte d'âge moyen, Femelle, Glycoprotéine de spicule des coronavirus, Humains, Mâle, Sensibilité et spécificité, Syndrome respiratoire aigu sévère, Test ELISA, Virus du SRAS.
English descriptors
- KwdEn :
- Adolescent, Adult, Antibodies, Viral (blood), Enzyme-Linked Immunosorbent Assay, Female, Humans, Immunoglobulin G (blood), Male, Membrane Glycoproteins (genetics), Membrane Glycoproteins (immunology), Middle Aged, Recombinant Proteins (genetics), Recombinant Proteins (immunology), SARS Virus, Sensitivity and Specificity, Severe Acute Respiratory Syndrome, Spike Glycoprotein, Coronavirus, Viral Envelope Proteins (genetics), Viral Envelope Proteins (immunology).
- MESH :
- chemical , blood : Antibodies, Viral, Immunoglobulin G.
- chemical , genetics : Membrane Glycoproteins, Recombinant Proteins, Viral Envelope Proteins.
- chemical , immunology : Membrane Glycoproteins, Recombinant Proteins, Viral Envelope Proteins.
- Adolescent, Adult, Enzyme-Linked Immunosorbent Assay, Female, Humans, Male, Middle Aged, SARS Virus, Sensitivity and Specificity, Severe Acute Respiratory Syndrome, Spike Glycoprotein, Coronavirus.
Abstract
Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450-650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera.
DOI: 10.1016/j.jcv.2004.09.024
PubMed: 15797360
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 002814
- to stream PubMed, to step Curation: 002814
- to stream PubMed, to step Checkpoint: 002753
Links to Exploration step
pubmed:15797360Le document en format XML
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450-650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15797360</PMID>
<DateCompleted><Year>2005</Year>
<Month>07</Month>
<Day>19</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>04</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">1386-6532</ISSN>
<JournalIssue CitedMedium="Print"><Volume>33</Volume>
<Issue>1</Issue>
<PubDate><Year>2005</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology</Title>
<ISOAbbreviation>J. Clin. Virol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus.</ArticleTitle>
<Pagination><MedlinePgn>12-8</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450-650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To develop and evaluate an ELISA system for detection of anti-S Abs in patient sera.</AbstractText>
<AbstractText Label="STUDY DESIGN" NlmCategory="METHODS">Express recombinant S450-650 in E. Coli and evaluate the sensitivity and specificity of an ELISA system based on the S450-650 polypeptide.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The S450-650-based ELISA detected IgG Abs in 41 out of 51 serum samples from 22 hospitalized patients with probable SARS, a result closely correlated with that obtained with a virus-based ELISA (r = 0.75, k = 0.8). Differential anti-S IgG responses were observed amongst SARS patients. Some of them produced anti-S Abs early during their infection, while others failed to make IgG Abs against the S450-650 polypeptide. None of the serum samples from 100 healthy blood donors was positive in the S450-650-based assay.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The S450-650-based ELISA can detect anti-S IgG Abs with high sensitivity and specificity.</AbstractText>
</Abstract>
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<ForeName>Jincun</ForeName>
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<AffiliationInfo><Affiliation>Department of Immunology, Peking University Health Science Center, 38 Xueyuan Road, Beijing 100083, PR China.</Affiliation>
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<ForeName>Wei</ForeName>
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<ForeName>Guang-Fa</ForeName>
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<Author ValidYN="Y"><LastName>Li</LastName>
<ForeName>Yonghua</ForeName>
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<ForeName>Xiaoyuan</ForeName>
<Initials>X</Initials>
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<Author ValidYN="Y"><LastName>Ren</LastName>
<ForeName>Furong</ForeName>
<Initials>F</Initials>
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<Author ValidYN="Y"><LastName>Zhao</LastName>
<ForeName>Zhendong</ForeName>
<Initials>Z</Initials>
</Author>
<Author ValidYN="Y"><LastName>Gao</LastName>
<ForeName>Xiao-Ming</ForeName>
<Initials>XM</Initials>
</Author>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D023362">Evaluation Study</PublicationType>
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<affiliations><list><country><li>République populaire de Chine</li>
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<settlement><li>Pékin</li>
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<tree><noCountry><name sortKey="Gao, Xiao Ming" sort="Gao, Xiao Ming" uniqKey="Gao X" first="Xiao-Ming" last="Gao">Xiao-Ming Gao</name>
<name sortKey="Li, Yonghua" sort="Li, Yonghua" uniqKey="Li Y" first="Yonghua" last="Li">Yonghua Li</name>
<name sortKey="Ren, Furong" sort="Ren, Furong" uniqKey="Ren F" first="Furong" last="Ren">Furong Ren</name>
<name sortKey="Wang, Guang Fa" sort="Wang, Guang Fa" uniqKey="Wang G" first="Guang-Fa" last="Wang">Guang-Fa Wang</name>
<name sortKey="Wang, Wei" sort="Wang, Wei" uniqKey="Wang W" first="Wei" last="Wang">Wei Wang</name>
<name sortKey="Xu, Xiaoyuan" sort="Xu, Xiaoyuan" uniqKey="Xu X" first="Xiaoyuan" last="Xu">Xiaoyuan Xu</name>
<name sortKey="Zhao, Zhendong" sort="Zhao, Zhendong" uniqKey="Zhao Z" first="Zhendong" last="Zhao">Zhendong Zhao</name>
<name sortKey="Zhuang, Hui" sort="Zhuang, Hui" uniqKey="Zhuang H" first="Hui" last="Zhuang">Hui Zhuang</name>
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<country name="République populaire de Chine"><noRegion><name sortKey="Zhao, Jincun" sort="Zhao, Jincun" uniqKey="Zhao J" first="Jincun" last="Zhao">Jincun Zhao</name>
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