Abstract
In this manuscript, an E1 and E3 deleted adenoviral recombinant expressing the rabies virus glycoprotein (G protein) under the control of the cytomegalovirus early promoter was tested for induction of a rabies virus-specific immune response in mice. The construct was found to induce neutralizing antibodies and cytolytic T cells to rabies virus. Mice vaccinated with the adenoviral construct either by the systemic route or by application into the airways were protected against a subsequent infection with a virulent strain of rabies virus. The efficacy of the replication-defective construct was far superior to that of a well-characterized vaccinia rabies glycoprotein recombinant.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adenovirus E1 Proteins / genetics
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Adenovirus E3 Proteins / genetics
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Adenoviruses, Human / genetics
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Adenoviruses, Human / immunology*
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Adenoviruses, Human / physiology
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Animals
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Antibodies, Viral / immunology
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B-Lymphocytes / immunology
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Cell Line
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Cricetinae
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Disease Models, Animal
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Female
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Genetic Vectors / genetics
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Genetic Vectors / immunology*
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HeLa Cells
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Humans
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C3H
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Mice, Inbred ICR
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Rabies / immunology
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Rabies / prevention & control*
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Rabies Vaccines / administration & dosage
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Rabies Vaccines / genetics
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Rabies Vaccines / immunology*
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Rabies virus / genetics
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Rabies virus / immunology*
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T-Lymphocytes / cytology
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T-Lymphocytes / immunology
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T-Lymphocytes, Cytotoxic / immunology
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Vaccines, Synthetic / administration & dosage
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Vaccines, Synthetic / genetics
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Vaccines, Synthetic / immunology*
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Virus Replication
Substances
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Adenovirus E1 Proteins
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Adenovirus E3 Proteins
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Antibodies, Viral
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Rabies Vaccines
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Vaccines, Synthetic
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adenovirus 5, rabies glycoprotein recombinant vaccine