Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/62950
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Type: Journal article
Title: Induction of both cellular and humoral immunity following a rational prime-boost immunization regimen that incorporates recombinant ovine atadenovirus and fowlpox virus
Author: Fraser, C.
Diener, K.
Lousberg, E.
Both, G.
Ward, L.
Brown, M.
Hayball, J.
Citation: Clinical and Vaccine Immunology, 2010; 17(11):1679-1686
Publisher: American Society for Microbiology
Issue Date: 2010
ISSN: 1556-6811
1556-679X
Statement of
Responsibility: 
Cara K. Fraser, Kerrilyn R. Diener, Erin L. Lousberg, Gerald W. Both, Larry Ward, Michael P. Brown and John D. Hayball
Abstract: Recombinant fowlpox viruses (rFPV) and ovine atadenoviruses (rOAdV) are being developed as safe, nonpathogenic, prophylactic and therapeutic vaccine vectors. There is scope, however, to improve the limited immune responses elicited by each of these vaccine vectors. Using previously determined and optimized routes of administration and viral doses, we characterized the primary adaptive immune responses elicited by recombinant variants of each virus. We demonstrate the contrasting nature of the response elicited by each recombinant virus. Whereas rFPV generates predominately cell-mediated immunity to our nominal target antigen, ovalbumin (OVA), rOAdV drives strong humoral responses. By defining the time taken to achieve maximal cytotoxic T cell responses and by studying the different patterns and kinetics of major histocompatibility complex class I-restricted OVA antigen expression postimmunization, we proposed a heterologous prime-boost regimen of immunization with rOAdV followed by rFPV. The subsequent experimental results showed that this approach produced robust cell-mediated and humoral immune responses against OVA that, importantly, were accompanied by weak anti-viral vector antibody responses. These results, therefore, represent a novel and potentially clinically applicable way to achieve broadly based and effective immunity to the antigens encoded by vectored vaccines.
Keywords: T-Lymphocytes, Cytotoxic
Animals
Mice, Inbred C57BL
Mice
Atadenovirus
Fowlpox virus
Ovalbumin
Vaccines, Synthetic
Viral Vaccines
Antibodies, Viral
Drug Carriers
Immunization, Secondary
Vaccination
Genetic Vectors
Rights: Copyright © 2010, American Society for Microbiology. All Rights Reserved.
DOI: 10.1128/CVI.00291-10
Grant ID: http://purl.org/au-research/grants/arc/LP0561810
Appears in Collections:Aurora harvest
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