Delivery of antigenic candidates by a DNA/MVA heterologous approach elicits effector CD8T cell mediated immunity against Trypanosoma cruzi

In this study, we have characterized the immune mechanisms elicited by antigenic candidates, TcG2 and TcG4, delivered by a DNA-prime/MVA-boost approach, and evaluated the host responses to Trypanosoma cruzi infection in C57BL/6 mice. Immunization of mice with antigenic candidates elicited antigen-specific, high-avidity, trypanolytic antibody response (IgG2b > IgG1) and CD8⁺T cells that exhibited type-1 cytolytic effector (CD8⁺CD107a⁺IFN-γ⁺Perforin⁺) phenotype. The extent of TcG2-dependent type 1 B and T cell immunity was higher than that noted in TcG4-immunized mice, and expanded accordingly in response to challenge infection with T. cruzi. The progression of chronic phase in immunized mice was associated with persistence of IgGs, 55–90% reduction in the frequency of proinflammatory (IFN-γ⁺ or TNF-α⁺) CD8⁺T cells, and an increase or emergence of immunoregulatory (IL-10⁺) CD4/CD8 T cells. The tissue parasitism, infiltration of inflammatory infiltrate, parasite persistence, and fibrosis were decreased by 82–92% in heart and skeletal muscle of immunized/chronically infected mice. Control mice exhibited a significantly low antibody response, consistent activation of effector CD8⁺T cells dominated by pro-inflammatory phenotype and mixed cytokine profile (IFN-γ + TNF-α > IL-4 + IL-10), parasite persistence and pathologic damage in chagasic hearts. We conclude that delivery of TcG2 or TcG4 by DNA-rMVA approach elicits effective antibody and CD8⁺T cell mediated immunity against T. cruzi and Chagas disease. The emergence of type 2 cytokine and T cell response in chronic phase was indicative of prevention of clinical disease.