Abstract
Epitopes containing the residues 141aa-160aa and 200aa-213aa from foot-and-mouth disease (FMD) serotype O1K HK type FMDV VP1 were joined to a swine immunoglobulin G single heavy chain constant region (scIgG), creating a novel chimeric protein, named F1-scIgG. In this study, inoculation with F1-scIgG induced both FMD virus-neutralizing antibody response and T cell response in swine. Antisera from these F1-scIgG-inoculated swine protected suckling mice against 1000 lethal dose 50 (1000LD(50)) FMD challenge. F1-scIgG-inoculated swine were also fully protected against 50LD(50) FMD virus challenge. The present study demonstrates the clear potential for viral epitopes linked with self-Ig in novel FMD vaccine design.
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, Viral / biosynthesis
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Antigens, Viral / chemistry
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Antigens, Viral / genetics
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Aphthovirus / genetics
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Aphthovirus / immunology*
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Base Sequence
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DNA Primers / genetics
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Epitopes / chemistry
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Epitopes / genetics
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Foot-and-Mouth Disease / prevention & control
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Immunoglobulin G / chemistry
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Immunoglobulin G / genetics
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Immunoglobulin G / immunology*
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In Vitro Techniques
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Lymphocyte Activation
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Mice
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Neutralization Tests
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Recombinant Fusion Proteins / chemistry
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / immunology
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Swine
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T-Lymphocytes / immunology
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Viral Vaccines / genetics
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Viral Vaccines / immunology
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Viral Vaccines / pharmacology
Substances
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Antibodies, Viral
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Antigens, Viral
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DNA Primers
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Epitopes
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Immunoglobulin G
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Recombinant Fusion Proteins
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Viral Vaccines