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Parenteral vaccination of mammalian livestock with Newcastle disease virus-based vector vaccines offers optimal efficacy and safety
- Source :
- Bioengineered Bugs 2 (2011) 1, Bioengineered Bugs, 2(1), 58-62
- Publication Year :
- 2011
- Publisher :
- Informa UK Limited, 2011.
-
Abstract
- Newcastle disease virus (NDV) is an avian virus that is being evaluated as a vaccine vector for the delivery of foreign genes in mammals. The use of NDV as a vaccine vector in these species offers two major advantages. First, NDV is highly attenuated in mammals, rendering its use inherently safe. Second, mammals lack pre-existing NDV immunity, which minimizes the risk of vaccination failure. NDV-vector vaccines are generally administered to mammals via the respiratory route. We recently showed that intramuscular vaccination with NDV-based Rift Valley fever virus (RVFV) vaccines provides complete protection in mice and induces neutralizing antibodies in sheep and cattle, the main target species of RVFV. Here, we discuss the use of NDV as a vaccine vector for applications in mammalian livestock with an emphasis on the vaccination route. We also report the results of novel experiments that underscore our notion that vaccination via a parenteral route is more effective than immunization via the respiratory route.
- Subjects :
- Vaccine safety
Livestock
animal structures
viruses
animal diseases
Newcastle disease virus
Rift valley fever virus
Bioengineering
Applied Microbiology and Biotechnology
Newcastle disease
Virus
Mice
Paramyxovirus
Immunity
Vector vaccine
Animals
Vector (molecular biology)
Intramuscular
Sheep
biology
Subcutaneous
Viral Vaccine
Vaccination
Viral Vaccines
biochemical phenomena, metabolism, and nutrition
biology.organism_classification
Virology
Immunity, Humoral
Virology & Molecular Biology
Virologie & Moleculaire Biologie
Humoral immunity
Immunization
embryonic structures
Immunology
biology.protein
Cattle
Vaccination route
Antibody
Vaccine
Biotechnology
Subjects
Details
- ISSN :
- 19491026 and 19491018
- Volume :
- 2
- Database :
- OpenAIRE
- Journal :
- Bioengineered Bugs
- Accession number :
- edsair.doi.dedup.....a7722128186a7ee50dec3c17fd4a9ba8
- Full Text :
- https://doi.org/10.4161/bbug.2.1.13349