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Heat-killed cps is an inactivated preparation of the Toxoplasma gondii cps strain, which is a non-replicating uracil auxotroph created by deleting the carbamoyl phosphate synthetase II (CPS) gene. Developed at the Geisel School of Medicine at Dartmouth, this agent is primarily utilized in preclinical research as a negative control to investigate the mechanisms of parasite-based immunotherapy. While the live, invasion-competent cps strain triggers a robust Th1-dependent anti-tumor immune response involving IL-12 production, IFNγ secretion, and CD8+ T cell activation, the heat-killed version is unable to actively invade host cells. Consequently, it fails to elicit these protective immune mechanisms and does not provide a survival advantage in models of disseminated pancreatic cancer, demonstrating that active cellular invasion is a prerequisite for the strain's therapeutic efficacy.
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