Generation of Trypanosoma cruzi -Specific CD8 + T-Cell Immunity Is Unaffected by the Absence of Type I Interferon Signaling

Abstract

ABSTRACT Trypanosoma cruzi is a protozoan parasite that causes human Chagas’ disease, a leading source of congestive heart failure in Central and South America. CD8 + T cells are critical for control of T. cruzi infection, and CD8 + T cells recognizing the immunodominant trans -sialidase gene-encoded peptide TSKB20 (ANYKFTLV) account for approximately 30% of the total CD8 + T-cell population at the peak of infection in C57BL/6 mice. Type I interferons (IFN-I) are pleiotropic cytokines that play a critical role in both innate and adaptive immunity against a variety of infections, but their induction and their role in infection are dictated by the infectious agent. Because type I IFNs and IFN-responsive genes are evident early after T. cruzi infection of host cells, we examined the influence of IFN-I on the development of CD8 + T-cell responses during this infection. Mice lacking the receptor for IFN-I (IFNARKO) and their wild-type counterparts both developed chronic infections and generated similar frequencies of immunodominant TSKB20- and subdominant TSKB18-specific CD8 + T cells following T. cruzi infection. In contrast, peak TSKB20-specific CD8 + T-cell responses generated during infection with vaccinia virus engineered to express TSKB20 were approximately 2.5-fold lower in IFNARKO mice than B6 mice, although after viral clearance, the frequencies of TSKB20-specific CD8 + T cells stabilized at similar levels. Together, these data suggest that IFN-I induction and biology are dependent upon the microbial context and emphasize the need to investigate various infection models for a full understanding of CD8 + T-cell development.