Overall, the DNA vaccine pVAX1–TgCyP induced a significantly higher level of humoral response and splenocyte click here proliferation in BALB/c mice. A higher survival rate was attained in the pVAX1–TgCyP vaccinated group compared with the control groups. From these results, we believe that TgCyP can be an alternative vaccine

antigen for preventing T. gondii infection. In recent years, vaccine studies have predominated in the quest to prevent toxoplasmosis. Specific immune responses and efficient production have been induced in mice by DNA vaccines that have been constructed with different T. gondii antigens, including SAG1, AMA1, IMP1, ADF and MIC3 [10-13]. Cyclophilins are known to be molecular chaperones, suggesting that TgCyP and certain parasite peptides or other molecules may together engage the chemokine receptor CCR5 and a TLR molecule to trigger high production of IL-12 [17, 23-25]. Recombinant TgCyP has also been shown to have potent PPIase and IL-12-inducing activities,

thus promoting the stabilization of the T. gondii life cycle and preventing T. gondii from overwhelming its intermediate learn more hosts [17]. Furthermore, NcCyP has been shown to enhance IL-12 and IFN-γ production in dendritic cells [18]. IFN-γ, which produced by T cells and NK cells, is up-regulated by IL-12, and it is one of the most critical cytokines that mediates host protection against infection by T. gondii. In this study, the parasite antigen TgCyP was investigated as an initiation immunoregulatory molecule and was expected to trigger an antigen-specific

immune response to T. gondii by inducing IL-12 and IFN-γ. A TgCyP-specific antibody was detected in mice immunized with pVAX1–TgCyP. The survival rate after challenge with tachyzoites increased, suggesting that there is a correlation between a high anti-TgCyP antibody level and protection. Splenocytes consist of a variety of cell populations, such as B cells, T cells, dendritic cells and macrophages, all of which Olopatadine take part in several immune responses to intracellular parasite infection. Due to the high similarity between TgCyP and NcCyP, the high splenocyte proliferation in the pVAX1–TgCyP-vaccinated mice suggest that TgCyP could increase the proliferation of dendritic cells and antigen-specific CD4+ T cells, which has been previously verified for NcCyP antigen[19]. To further characterize the polarization of the immune response, we evaluated IL-2, IL-4, IL-10 and IFN-γ as indications of the Th1 and Th2 responses. IL-2 is produced primarily by T cells that express the surface antigen CD4 following allogenic activation. IL-2 is also a growth factor for all subpopulations of T-lymphocytes. T. gondii is a protozoan that is susceptible to the T-cell immunosuppressive agent cyclosporin A (CsA), and the activity of TgCyP and IL-2 synthesis in vitro has been shown to be suppressed by CsA [16].