Toxoplasma gondii is a common parasite which causes the development of fatal encephalosis or pneumonia in immunodeficient patients under treatment of AIDS or cancer.
Pregnant women who are infected may suffer a miscarriage or the newborn child may suffer from a congenital disease. Currently, a toxoplasma vaccine for humans is not available. Using experimental animals such as mice, basic research for developing an inactivated vaccine is underway.
This group's achievement is expected to offer strategies for developing a toxoplasma-inactivated vaccine targeting p62 for treating toxoplasmosis, whose case reports have been on the rise in Japan in recent years. From a prior study which found that the antigens derived from the toxoplasma emitted within the parasitophorous vacuole become the major antigens for the killer T cells, Professor Yamamoto's group investigated the activation of killer T cells when the toxoplasma-infected cells were stimulated by interferon-γ (IFN-γ).
As a result, it was found that the activity of antigen-specific killer T cells in infected cells that were stimulated by IFN-γ was dramatically higher than in non-stimulated infected cells. This robust activation of killer T cells seen when these infected cells undergo IFN-γ stimulation was significantly reduced in mice with p62 deficiencies. Even on an individual level, when compared with wild-type mice, there was a sharp decrease in antigen-specific killer T cells in p62 deficient mice when administered the toxoplasma-inactivated vaccine.
These findings clarified that IFN-γ-dependent p62 has the unique role of gathering in the parasitophorous vacuole of toxoplasma through IFN-γ stimulation and activating the antigen-specific killer T cells released within the parasitophorous vacuole, a world first.