Abstract
We identified the domains of CD26 involved in the binding of Middle East respiratory syndrome coronavirus (MERS-CoV) using distinct clones of anti-CD26 monoclonal antibodies (MAbs). One clone, named 2F9, almost completely inhibited viral entry. The humanized anti-CD26 MAb YS110 also significantly inhibited infection. These findings indicate that both 2F9 and YS110 are potential therapeutic agents for MERS-CoV infection. YS110, in particular, is a good candidate for immediate testing as a therapeutic modality for MERS.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antibodies, Monoclonal / immunology*
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Antibodies, Monoclonal / pharmacology
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Antibodies, Viral / immunology*
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Antibodies, Viral / pharmacology
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Coronaviridae / drug effects
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Coronaviridae / genetics
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Coronaviridae / physiology*
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Coronaviridae Infections / drug therapy
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Coronaviridae Infections / enzymology*
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Coronaviridae Infections / immunology
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Coronaviridae Infections / virology*
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Dipeptidyl Peptidase 4 / chemistry
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Dipeptidyl Peptidase 4 / genetics
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Dipeptidyl Peptidase 4 / immunology*
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Epitope Mapping
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Humans
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Protein Binding
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Protein Structure, Tertiary
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Spike Glycoprotein, Coronavirus / genetics
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Spike Glycoprotein, Coronavirus / metabolism
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Virus Internalization / drug effects
Substances
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Antibodies, Monoclonal
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Antibodies, Viral
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Spike Glycoprotein, Coronavirus
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Dipeptidyl Peptidase 4