Highly competent, non-exhausted CD8+T cells continue to tightly control pathogen load throughout chronic Trypanosoma cruzi infection

Trypanosoma cruzi infection is characterized by chronic parasitism of non-lymphoid tissues and is rarely eliminated despite potent adaptive immune responses. This failure to cure has frequently been attributed to a loss or impairment of anti-T. cruzi T cell responses over time, analogous to the T cell dysfunction described for other persistent infections. In this study, we have evaluated the role of CD8(+) T cells during chronic T. cruzi infection (>100 dpi), with a focus on sites of pathogen persistence. Consistent with repetitive antigen exposure during chronic infection, parasite-specific CD8(+) T cells from multiple organs expressed high levels of KLRG1, but exhibit a preferential accumulation of CD69(+) cells in skeletal muscle, indicating recent antigen encounter in a niche for T. cruzi persistence. A significant proportion of CD8(+) T cells in the muscle also produced IFN gamma, TNF alpha and granzyme B in situ, an indication of their detection of and functional response to T. cruzi in vivo. CD8(+) T cell function was crucial for the control of parasite burden during chronic infection as exacerbation of parasite load was observed upon depletion of this population. Attempts to improve T cell function by blocking PD-1 or IL-10, potential negative regulators of T cells, failed to increase IFN gamma and TNF alpha production or to enhance T. cruzi clearance. These results highlight the capacity of the CD8(+) T cell population to retain essential in vivo function despite chronic antigen stimulation and support a model in which CD8(+) T cell dysfunction plays a negligible role in the ability of Trypanosoma cruzi to persist in mice.