Abstract
E1-deleted adenoviral vectors of the human serotype 5 (AdHu5) and the chimpanzee serotype 68 (AdC68) expressing the rabies virus glycoprotein (rab.gp) were tested for induction of transgene product-specific Abs upon intranasal or oral immunization of newborn mice. Both vectors induced Abs to rabies virus that could be detected in serum and from mucosal secretions. Serum rabies virus neutralizing Ab titers sufficed to protect neonatally vaccinated mice against a subsequent challenge with rabies virus. The efficacy of the AdHu5rab.gp vector given orally to newborn mice born to AdHu5 virus-immune dams was not impaired by maternally transferred Abs to the vaccine carrier.
Publication types
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Research Support, Non-U.S. Gov't
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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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Adenoviruses, Human / genetics
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Adenoviruses, Human / immunology*
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Administration, Intranasal
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Administration, Oral
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Animals
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Animals, Newborn / immunology*
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Antibodies, Viral / biosynthesis*
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B-Lymphocytes / immunology
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B-Lymphocytes / metabolism
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Female
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Genetic Vectors / immunology
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Immunity, Maternally-Acquired / genetics
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Immunity, Maternally-Acquired / immunology
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Male
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Mice
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Mice, Inbred ICR
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Mouth Mucosa / immunology*
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Nasal Mucosa / immunology*
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Pan troglodytes
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Pregnancy
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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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Serotyping
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Transgenes / immunology*
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Vaccines, Synthetic / administration & dosage
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Vaccines, Synthetic / genetics
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Vaccines, Synthetic / immunology
Substances
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Adenovirus E1 Proteins
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Antibodies, Viral
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Rabies Vaccines
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Vaccines, Synthetic