, an obligate intracellular protozoan parasite, establishes a chronic infection by forming cysts preferentially in the brain. Up to one third of the human population worldwide is estimated to be chronically infected with this parasite. However, there is currently no drug effective against the cyst form of the parasite. In addition, the protective immunity against the cysts remains largely unknown. We analyzed the molecular mechanisms by which the immune system detects host cells harboring the cysts to eliminate the latent stage of the parasite using mice with the H-2 haplotype, which are genetically resistant to the infection. Our study revealed that CD8 immune T cells bearing TCR Vβ8.1, 8.2 chain have a potent activity to remove cysts from the brain. Our studies also uncovered that H-2L is the major Ag-presenting molecule to CD8 T cells for initiating cyst elimination, and that CD8Vβ8.1, 8.2 immune T cells recognize the N-terminal region (aa 41-152) of dense granule protein 6 (GRA6Nt) of the parasite presented by the H-2L molecule. Furthermore, CD8 immune T cells induced by immunization with recombinant GRA6Nt were eventually capable of removing the cysts from the brain when transferred to infected immunodeficient mice lacking T cells. Thus, GRA6Nt is a novel and potent Ag to activate CD8 T cells capable of removing cysts. These observations offer a basis for immunological intervention to combat chronic infection with by targeting the persistent cysts of the parasite.