When we analysed the cytokines induced by immunization with recombinant proteins, it was found that rTcSPA, rTcSPR and rTcSPC induced Th1- and Th2-type cytokines and rTcSP induced Th2-type cytokines, while the four proteins induced the proinflammatory cytokines IL-6 and TNF. When the mice were immunized with naked DNA, the cytokine levels were lower than those detected after

immunization with the recombinant proteins, and cytokines were not detected after immunization with pBKTcSPC. Immunization with the plasmids pBKTcSP or pBKTcSPA induced a mixed Th1/Th2 T-cell response, and immunization with pBKTcSPR induced IL-10 and IFN-γ. The proinflamatory cytokine IL-6 was induced by three plasmids. However, the survival rate of the immunized mice at 60 days was very low in the mice immunized with recombinant proteins and variable in Silmitasertib ic50 the mice immunized with naked DNA.

Combining the decreased parasitemia and increased survival rate, the plasmids protected parasite infected mice in the following order: pBKTcSPR > pBKTcSPC > pBKTcSP > pBKTcSPA. The mice immunized with pBKTcSPR showed induction of IL-10 and IFN-γ. IL-10 is a cytokine that stimulates NK cells and promotes the recruitment of macrophages and neutrophils [50], while Dolichyl-phosphate-mannose-protein mannosyltransferase IFN-γ is required to activate macrophages and indirectly constitutes an important source of protective proinflammatory cytokines, which can effectively kill intracellular parasites such as T. cruzi Roscovitine purchase by nitric oxide (NO) dependent mechanisms [51]. However, significantly higher levels of IFN-γ were detected in the groups immunized with pBKTcSP and pBKTcSPA, which showed no reduction in parasitemia. Therefore, other factors may be involved in the reduction

of parasitemia. One of these factors could be IL-10, as it can participate as an immunoregulatory cytokine in the Th1 response [52], thereby preventing collateral damage generated by a strong immune response against the parasite and suppressing the development of inflammatory cell infiltrate that otherwise would be exacerbated. Therefore, resolution of T. cruzi infections depends on the host’s ability to mount a protective immune response. It has been proposed that an exacerbated response to infections may result in deleterious lesions [53]. One of the main differences detected in the mice immunized with pBKTcSPR compared with the other mice that were immunized with DNA or protein is the low level of serum IL-10. It has been shown that IL-10 increases host susceptibility to intracellular and extracellular micro-organisms.