Author
BURGESS, B - MISSISSIPPI STATE UNIV | |
BAATEN, B - COMPTON UK IAH | |
BAXENDALE, W - INTERVET UK LTDS UK | |
DAVIS, P - INTERVET UK LTDS UK | |
HUNT, L - MISSISSIPPI STATE UNIV | |
Lee, Lucy | |
ROSS, L - COMPTON UK IAH | |
SONDERMEIJER, P - INTERVET NETHERLANDS | |
TARPEY, I - INTERVET UK | |
YOUNG, J - COMPTON UK IAH |
Submitted to: Workshop on Molecular Pathogenesis of Marek's Disease and Avian Immunology
Publication Type: Abstract Only Publication Acceptance Date: 10/11/2002 Publication Date: 10/11/2002 Citation: Burgess, B.C., Baaten, B.J., Baxendale, W., Davis, P.J., Hunt, L., Lee, L.F., Ross, L.N., Sondermeijer, P.J., Tarpey, I., Young, J.R. 2002. Marek's disease: a biomedical model for identifying molecular mechanisms critical to lymphocyte neoplastic transformation and anti-lymphoma immunity [abstract]. Workshop on Molecular Pathogenesis of Marek's Disease and Avian Immunology. p. 40. Interpretive Summary: Technical Abstract: We identify that, in common with human lymphomas of both viral and non-viral etiology, the Hodgkin's disease antigen (non-mutated CD30) is over-expressed by the neoplastically-transformed cells in Marek's Disease (MD) lymphomas and other lymphomagenic chicken viruses. Data presented here showed that CD30 is immunogenic during MD and that this immunogenicity may be used to advantage in MDV vaccines. Vaccination against an aberrantly expressed host antigen in an infectious disease is novel in any system and may decrease direct immune selective pressure on pathogens and improve long-term vaccine sustainability. |