Abstract
We evaluated the efficacy of three SARS vaccine candidates in a murine SARS model utilizing low-virulence Pp and SARS-CoV coinfection. Vaccinated mice were protected from severe respiratory disease in parallel with a low virus titer in the lungs and a high neutralizing antibody titer in the plasma. Importantly, the administration of spike protein-specific neutralizing monoclonal antibody protected mice from the disease, indicating that the neutralization is sufficient for protection. Moreover, a high level of IL-6 and MCP-1 production, but not other 18 cytokines tested, on days 2 and 3 after SARS-CoV infection was closely linked to the virus replication and disease severity, suggesting the importance of these cytokines in the lung pathogenicity of SARS-CoV infection.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies, Monoclonal / immunology
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Antibodies, Viral / immunology*
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Body Weight
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Chemokine CCL2 / analysis
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Disease Models, Animal
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Interleukin-6 / analysis
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Membrane Glycoproteins / immunology*
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Mice
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Mice, Inbred BALB C
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Neutralization Tests
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Severe Acute Respiratory Syndrome / immunology
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Severe Acute Respiratory Syndrome / prevention & control*
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Severe Acute Respiratory Syndrome / virology
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Severe acute respiratory syndrome-related coronavirus / immunology*
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Severe acute respiratory syndrome-related coronavirus / physiology
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Spike Glycoprotein, Coronavirus
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Vaccines, Inactivated
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Viral Envelope Proteins / immunology*
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Viral Vaccines / immunology*
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Virus Replication
Substances
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Antibodies, Monoclonal
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Antibodies, Viral
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Chemokine CCL2
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Interleukin-6
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Membrane Glycoproteins
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Spike Glycoprotein, Coronavirus
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Vaccines, Inactivated
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Viral Envelope Proteins
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Viral Vaccines
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spike glycoprotein, SARS-CoV