Enhanced protective response and immuno-adjuvant effects of porcine GM-CSF on DNA vaccination of pigs against Aujeszky’s disease virus

• Published in: Veterinary immunology and immunopathology 1999-09, Vol.70 (3), p.277-287
• Main Authors: Somasundaram, C., Takamatsu, H., Andréoni, C., Audonnet, J.-C., Fischer, L., Lefèvre, F., Charley, B.
• Format: Article
• Language: English
• Subjects: ADJUVANT; ADJUVANTS; Adjuvants, Immunologic; Animals; Antibodies, Viral - biosynthesis; AUJESZKY VIRUS; Aujeszky's disease virus; Cell Line; CERDO; CHO Cells; CITOQUININAS; COADYUVANTES; Cricetinae; Cytokines; CYTOKININE; CYTOKININS; DNA vaccination; GM-CSF; Granulocyte-Macrophage Colony-Stimulating Factor - immunology; IFN-γ; IL-2; IMMUNE RESPONSE; IMMUNISATION; IMMUNIZATION; INMUNIZACION; Life Sciences; Pigs; PORCIN; Porcine respiratory syncytial virus; Pseudorabies - immunology; Pseudorabies - prevention & control; Pseudorabies virus; Rabbits; REPONSE IMMUNITAIRE; RESPUESTA INMUNOLOGICA; SWINE; Transfection; VACCINATION; Vaccines, DNA; VACUNACION; Viral Vaccines; VIRUS D'AUJESZKY; VIRUS DE AUJESZKY
• ISSN: 0165-2427; 1873-2534
• DOI: 10.1016/S0165-2427(99)00085-9

This study was conducted to investigate whether the co-delivery of DNA encoding porcine cytokines would enhance a protective immune response in pigs to a Pseudorabies virus (PRV; or Aujeszky’s disease virus) DNA vaccine. Aujeszky’s disease in pigs results in respiratory and nervous symptoms with important economic losses. To evaluate cytokine effects, eukaryotic expression vectors were constructed for porcine GM-CSF, IL-2 and IFN-γ. cDNA for each of these cytokines was inserted under the control of a CMV promoter in the pcDNA3 plasmid and cytokine expression was confirmed after DNA transfection in various mammalian cell cultures by bioassays (GM-CSF and IL2) and ELISA (IFN-γ). Pigs were vaccinated by single intramuscular injection with plasmid DNA encoding PRV gB and gD along with various combinations of cytokine plasmid constructs. Pig serum was tested for the production of antibody by isotype specific anti-PRV ELISA. Pigs were then challenged with the highly virulent PRV strain NIA3 on day 21 after vaccination. The survival and growth rate of pigs were monitored for seven days after the viral challenge. The co-administration of GM-CSF plasmid increased the immune response induced by gB and gD PRV DNA vaccine. This immune response was characterized by an earlier appearance of anti-PRV IgG2, a significantly enhanced anti-PRV IgG1 and IgG2 antibody response, a significantly decreased and shortened viral excretion in nasal swabs and an improved protection to the viral challenge. In contrast, the co-administration of porcine IL-2 or IFN-γ had no adjuvant effects. Our results thus demonstrate for the first time that the application of porcine GM-CSF gene in a DNA vaccine formulation can exert immuno-adjuvant and protective effects with single vaccination in the natural host pig against Aujeszky’s disease.