Key result
Immunization with the pBudCE4.1-ORF2/IL18 plasmid significantly increased T-lymphocyte proliferation and Th1 cytokine production, and markedly inhibited PCV2 replication compared to the pBudCE4.1-ORF2 vaccine.
Co-expression of porcine IL-18 with PCV2 ORF2 enhances the immunogenicity and protective efficacy of a PCV2 DNA vaccine in piglets.
Supports IL-18 as adjuvant for PCV2 DNA vaccines in piglets; leaves open field validation before swine practice.
In this study, two recombinant plasmids containing the ORF2 gene of porcine circovirus type 2 (PCV2) with or without porcine interleukin-18 (IL-18) were constructed and evaluated for their ability to protect piglets against PCV2 challenge. Transient expression of the plasmids in PK-15 cells could be detected using Western blot. Piglets were given two intramuscular immunizations 3 weeks apart and were challenged with a virulent Wuzhi strain of PCV2 at 42 days after the initial immunization. All animals vaccinated with pBudCE4.1-ORF2 or with pBudCE4.1-ORF2/IL18 developed PCV2-specific antibody and T-lymphocyte proliferative responses. The levels of T-lymphocyte proliferation in piglets immunized with pBudCE4.1-ORF2/IL18 were significantly higher than in those immunized with pBudCE4.1-ORF2, and pBudCE4.1-ORF2/IL18 stimulated a significantly increased production of IFN-γ and IL-2. Furthermore, PCV2 challenge experiments showed that the DNA vaccine-immunized groups can partially prevent PCV2 viremia and significantly reduce the amount of PCV2 virus in the lymphoid tissues, and the piglets immunized by pBudCE4.1-ORF2/IL18 exhibit a marked inhibition of PCV2 replication compared to the pBudCE4.1-ORF2 group. These data demonstrate that the plasmid pBudCE4.1-ORF2/IL18 may be an effective approach for increasing PCV2 DNA vaccine immunogenicity.
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Chen et al. (2014) studied Porcine circovirus type 2 (PCV2) infection (n=20). pBudCE4.1-ORF2/IL18 recombinant plasmid DNA vaccine vs. pBudCE4.1-ORF2, empty vector pBudCE4.1, and PBS was evaluated on PCV2 viremia and tissue antigen load (p=<0.05). Immunization with the pBudCE4.1-ORF2/IL18 plasmid significantly increased T-lymphocyte proliferation and Th1 cytokine production, and markedly inhibited PCV2 replication compared to the pBudCE4.1-ORF2 vaccine.
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