concanamycin-a has been researched along with Toxoplasmosis--Animal* in 1 studies
1 other study(ies) available for concanamycin-a and Toxoplasmosis--Animal
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Granule-dependent killing of Toxoplasma gondii by CD8+ T cells.
Immunization of mice with live bradyzoites of a low-virulent Beverley strain of Toxoplasma gondii has been shown to increase CD8+ T-cell mediated immunity against a highly virulent RH strain. We found that preimmunization with an RH homogenate further enhanced this immunity. Using this model, we investigated the mechanism of CD8+ T-cell mediated protection against T. gondii infection. Splenic cells from mice immunized with RH homogenate and live bradyzoites stimulated apoptosis of RH-infected J774A.1 macrophages in vitro, and at the same time, the immunization significantly suppressed the proliferation of parasites within macrophages, as assessed by measuring 3H-uracil uptake by the parasites. Splenic cells from the immunized mice produced larger amounts of interferon-gamma (IFN-gamma) than did naive splenic cells; however, the production of nitric oxide (NO) by RH-infected macrophages was not enhanced. The elimination of CD8+ T cells from splenic cells significantly reduced their inhibitory action on parasite proliferation as well as their cytotoxic activity against RH-infected macrophages, but it did not affect the production of IFN-gamma. Treatment of CD8+ T-enriched splenic cells from the immunized mice with concanamycin A, but not an anti-Fas ligand monoclonal antibody, significantly reduced their anti-proliferative and killing capabilities, suggesting that the CD8+ T cells induced by immunization with RH antigen and live bradyzoites of the Beverley strain may exert protection against T. gondii infection at least in part through granule-dependent cytotoxic activities. Topics: Animals; Anti-Bacterial Agents; Antibodies, Monoclonal; CD8-Positive T-Lymphocytes; Cell Culture Techniques; Cytotoxicity, Immunologic; Enzyme Inhibitors; Fas Ligand Protein; Immunization; Interferon-gamma; Macrolides; Macrophages; Membrane Glycoproteins; Mice; Mice, Inbred BALB C; Nitric Oxide; Proton-Translocating ATPases; Protozoan Vaccines; Spleen; Survival Rate; Toxoplasma; Toxoplasmosis, Animal; Virulence | 2001 |