Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.
Identifieur interne : 002464 ( PubMed/Corpus ); précédent : 002463; suivant : 002465Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.
Auteurs : Man Cheng ; Ceci W L. Chan ; Randy C F. Cheung ; Rama Kamesh Bikkavilli ; Qi Zhao ; Shannon W N. Au ; Paul K S. Chan ; Susanna S T. Lee ; Gregory Cheng ; Walter K K. Ho ; Wing-Tai CheungSource :
- Biochemical and biophysical research communications [ 0006-291X ] ; 2005.
English descriptors
- KwdEn :
- Animals, Antibodies, Viral (immunology), Base Sequence, Cell Line, Chlorocebus aethiops, Cross Reactions (immunology), Interleukin-11 (immunology), Mice, Molecular Sequence Data, Nucleocapsid Proteins (chemistry), Nucleocapsid Proteins (immunology), Rats, SARS Virus (chemistry), SARS Virus (immunology), Sequence Alignment, Sequence Homology, Nucleic Acid.
- MESH :
- chemical , chemistry : Nucleocapsid Proteins.
- chemical , immunology : Antibodies, Viral, Interleukin-11, Nucleocapsid Proteins.
- chemistry : SARS Virus.
- immunology : Cross Reactions, SARS Virus.
- Animals, Base Sequence, Cell Line, Chlorocebus aethiops, Mice, Molecular Sequence Data, Rats, Sequence Alignment, Sequence Homology, Nucleic Acid.
Abstract
Infection of SARS-associated coronavirus (SARS-CoV) induced a strong anti-nucleocapsid (anti-N) antibody response. However, the pathophysiological significance of the anti-N antibodies in SARS pathogenesis is largely unknown. To profile the anti-N antibodies, a phage-displayed scFv library was prepared from mice immunized with heat-inactivated SARS-CoV-infected Vero E6 cell lysate. Specific anti-N scFvs were isolated by panning against a recombinant nucleocapsid protein and reactivity was confirmed with phage-ELISA. Sequence analysis indicated that two of the isolated anti-N scFv clones were identical and displayed a high homology with an scFv specific for interleukin 11 (IL-11), an anti-inflammatory cytokine derived from bone marrow stroma cells. In a neutralization assay, IL-11-induced STAT 3 phosphorylation in rat intestinal epithelial IEC-18 cells was completely suppressed by the anti-N scFv clone L9N01.
DOI: 10.1016/j.bbrc.2005.10.088
PubMed: 16263078
Links to Exploration step
pubmed:16263078Le document en format XML
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Cheung</name></author><author><name sortKey="Bikkavilli, Rama Kamesh" sort="Bikkavilli, Rama Kamesh" uniqKey="Bikkavilli R" first="Rama Kamesh" last="Bikkavilli">Rama Kamesh Bikkavilli</name></author><author><name sortKey="Zhao, Qi" sort="Zhao, Qi" uniqKey="Zhao Q" first="Qi" last="Zhao">Qi Zhao</name></author><author><name sortKey="Au, Shannon W N" sort="Au, Shannon W N" uniqKey="Au S" first="Shannon W N" last="Au">Shannon W N. Au</name></author><author><name sortKey="Chan, Paul K S" sort="Chan, Paul K S" uniqKey="Chan P" first="Paul K S" last="Chan">Paul K S. Chan</name></author><author><name sortKey="Lee, Susanna S T" sort="Lee, Susanna S T" uniqKey="Lee S" first="Susanna S T" last="Lee">Susanna S T. Lee</name></author><author><name sortKey="Cheng, Gregory" sort="Cheng, Gregory" uniqKey="Cheng G" first="Gregory" last="Cheng">Gregory Cheng</name></author><author><name sortKey="Ho, Walter K K" sort="Ho, Walter K K" uniqKey="Ho W" first="Walter K K" last="Ho">Walter K K. Ho</name></author><author><name sortKey="Cheung, Wing Tai" sort="Cheung, Wing Tai" uniqKey="Cheung W" first="Wing-Tai" last="Cheung">Wing-Tai Cheung</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2005">2005</date><idno type="RBID">pubmed:16263078</idno><idno type="pmid">16263078</idno><idno type="doi">10.1016/j.bbrc.2005.10.088</idno><idno type="wicri:Area/PubMed/Corpus">002464</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002464</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.</title><author><name sortKey="Cheng, Man" sort="Cheng, Man" uniqKey="Cheng M" first="Man" last="Cheng">Man Cheng</name><affiliation><nlm:affiliation>Department of Biochemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.</nlm:affiliation></affiliation></author><author><name sortKey="Chan, Ceci W L" sort="Chan, Ceci W L" uniqKey="Chan C" first="Ceci W L" last="Chan">Ceci W L. Chan</name></author><author><name sortKey="Cheung, Randy C F" sort="Cheung, Randy C F" uniqKey="Cheung R" first="Randy C F" last="Cheung">Randy C F. Cheung</name></author><author><name sortKey="Bikkavilli, Rama Kamesh" sort="Bikkavilli, Rama Kamesh" uniqKey="Bikkavilli R" first="Rama Kamesh" last="Bikkavilli">Rama Kamesh Bikkavilli</name></author><author><name sortKey="Zhao, Qi" sort="Zhao, Qi" uniqKey="Zhao Q" first="Qi" last="Zhao">Qi Zhao</name></author><author><name sortKey="Au, Shannon W N" sort="Au, Shannon W N" uniqKey="Au S" first="Shannon W N" last="Au">Shannon W N. Au</name></author><author><name sortKey="Chan, Paul K S" sort="Chan, Paul K S" uniqKey="Chan P" first="Paul K S" last="Chan">Paul K S. Chan</name></author><author><name sortKey="Lee, Susanna S T" sort="Lee, Susanna S T" uniqKey="Lee S" first="Susanna S T" last="Lee">Susanna S T. Lee</name></author><author><name sortKey="Cheng, Gregory" sort="Cheng, Gregory" uniqKey="Cheng G" first="Gregory" last="Cheng">Gregory Cheng</name></author><author><name sortKey="Ho, Walter K K" sort="Ho, Walter K K" uniqKey="Ho W" first="Walter K K" last="Ho">Walter K K. Ho</name></author><author><name sortKey="Cheung, Wing Tai" sort="Cheung, Wing Tai" uniqKey="Cheung W" first="Wing-Tai" last="Cheung">Wing-Tai Cheung</name></author></analytic><series><title level="j">Biochemical and biophysical research communications</title><idno type="ISSN">0006-291X</idno><imprint><date when="2005" type="published">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Antibodies, Viral (immunology)</term><term>Base Sequence</term><term>Cell Line</term><term>Chlorocebus aethiops</term><term>Cross Reactions (immunology)</term><term>Interleukin-11 (immunology)</term><term>Mice</term><term>Molecular Sequence Data</term><term>Nucleocapsid Proteins (chemistry)</term><term>Nucleocapsid Proteins (immunology)</term><term>Rats</term><term>SARS Virus (chemistry)</term><term>SARS Virus (immunology)</term><term>Sequence Alignment</term><term>Sequence Homology, Nucleic Acid</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Nucleocapsid Proteins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Antibodies, Viral</term><term>Interleukin-11</term><term>Nucleocapsid Proteins</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>SARS Virus</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Cross Reactions</term><term>SARS Virus</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Base Sequence</term><term>Cell Line</term><term>Chlorocebus aethiops</term><term>Mice</term><term>Molecular Sequence Data</term><term>Rats</term><term>Sequence Alignment</term><term>Sequence Homology, Nucleic Acid</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Infection of SARS-associated coronavirus (SARS-CoV) induced a strong anti-nucleocapsid (anti-N) antibody response. However, the pathophysiological significance of the anti-N antibodies in SARS pathogenesis is largely unknown. To profile the anti-N antibodies, a phage-displayed scFv library was prepared from mice immunized with heat-inactivated SARS-CoV-infected Vero E6 cell lysate. Specific anti-N scFvs were isolated by panning against a recombinant nucleocapsid protein and reactivity was confirmed with phage-ELISA. Sequence analysis indicated that two of the isolated anti-N scFv clones were identical and displayed a high homology with an scFv specific for interleukin 11 (IL-11), an anti-inflammatory cytokine derived from bone marrow stroma cells. In a neutralization assay, IL-11-induced STAT 3 phosphorylation in rat intestinal epithelial IEC-18 cells was completely suppressed by the anti-N scFv clone L9N01.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16263078</PMID><DateCompleted><Year>2006</Year><Month>01</Month><Day>06</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>04</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0006-291X</ISSN><JournalIssue CitedMedium="Print"><Volume>338</Volume><Issue>3</Issue><PubDate><Year>2005</Year><Month>Dec</Month><Day>23</Day></PubDate></JournalIssue><Title>Biochemical and biophysical research communications</Title><ISOAbbreviation>Biochem. Biophys. Res. Commun.</ISOAbbreviation></Journal><ArticleTitle>Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.</ArticleTitle><Pagination><MedlinePgn>1654-60</MedlinePgn></Pagination><Abstract><AbstractText>Infection of SARS-associated coronavirus (SARS-CoV) induced a strong anti-nucleocapsid (anti-N) antibody response. However, the pathophysiological significance of the anti-N antibodies in SARS pathogenesis is largely unknown. To profile the anti-N antibodies, a phage-displayed scFv library was prepared from mice immunized with heat-inactivated SARS-CoV-infected Vero E6 cell lysate. Specific anti-N scFvs were isolated by panning against a recombinant nucleocapsid protein and reactivity was confirmed with phage-ELISA. Sequence analysis indicated that two of the isolated anti-N scFv clones were identical and displayed a high homology with an scFv specific for interleukin 11 (IL-11), an anti-inflammatory cytokine derived from bone marrow stroma cells. In a neutralization assay, IL-11-induced STAT 3 phosphorylation in rat intestinal epithelial IEC-18 cells was completely suppressed by the anti-N scFv clone L9N01.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Cheng</LastName><ForeName>Man</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Biochemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chan</LastName><ForeName>Ceci W L</ForeName><Initials>CW</Initials></Author><Author ValidYN="Y"><LastName>Cheung</LastName><ForeName>Randy C F</ForeName><Initials>RC</Initials></Author><Author ValidYN="Y"><LastName>Bikkavilli</LastName><ForeName>Rama Kamesh</ForeName><Initials>RK</Initials></Author><Author ValidYN="Y"><LastName>Zhao</LastName><ForeName>Qi</ForeName><Initials>Q</Initials></Author><Author ValidYN="Y"><LastName>Au</LastName><ForeName>Shannon W N</ForeName><Initials>SW</Initials></Author><Author ValidYN="Y"><LastName>Chan</LastName><ForeName>Paul K S</ForeName><Initials>PK</Initials></Author><Author ValidYN="Y"><LastName>Lee</LastName><ForeName>Susanna S T</ForeName><Initials>SS</Initials></Author><Author ValidYN="Y"><LastName>Cheng</LastName><ForeName>Gregory</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Ho</LastName><ForeName>Walter K K</ForeName><Initials>WK</Initials></Author><Author ValidYN="Y"><LastName>Cheung</LastName><ForeName>Wing-Tai</ForeName><Initials>WT</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2005</Year><Month>10</Month><Day>25</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Biochem Biophys Res 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