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Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.

Identifieur interne : 004876 ( Main/Exploration ); précédent : 004875; suivant : 004877

Cross-reactivity of antibody against SARS-coronavirus nucleocapsid protein with IL-11.

Auteurs : Man Cheng [République populaire de Chine] ; 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 Cheung

Source :

RBID : pubmed:16263078

Descripteurs français

English descriptors

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


Affiliations:


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<term>Cross Reactions (immunology)</term>
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<term>Mice</term>
<term>Molecular Sequence Data</term>
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<term>Nucleocapsid Proteins (immunology)</term>
<term>Rats</term>
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<term>Protéines nucléocapside ()</term>
<term>Protéines nucléocapside (immunologie)</term>
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<term>Réactions croisées (immunologie)</term>
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<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>
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