Correlation between Direct Binding Ability of SyntheticT. gondiiSAG1 Peptides to HLA-A2 Measured by a Sensor for Surface Plasmon Resonance and Antigenicity of the Peptides forT. gondii-Infected Cell-Specific CTL |
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Institution: | 1. National Hospital Organization Kyushu Medical Center, Fukuoka, Japan;2. The Cancer Institute Hospital of the Japanese Foundation of Cancer Research, Tokyo, Japan;3. Tokyo Women''s Medical University Hospital, Tokyo, Japan;4. Kobe City Medical Center General Hospital, Hyogo, Japan;5. AstraZeneca KK, Osaka, Japan;6. AstraZeneca KK, Tokyo, Japan. |
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Abstract: | Toxoplasma gondii(T. gondii) -infected B lymphoma cells presentT. gondiiantigens in the context of major histocompatibility complex molecules toT. gondii-specific CD8+cytotoxic T cells (CTL). HLA-A2 molecules ofT. gondii-infected human cells have been shown to be used in presenting T. gondiiantigens to CD8+CTL. SAG1, one of the major antigenic molecules ofT. gondii,is an antigen forT. gondii-specific CTL, and represents a possible basis for vaccines. The direct binding of nonamer SAG1 peptides to HLA-A2 was assayed here using an automated biosensor system with a sensor for surface plasmon resonance detection. The antigenicity of synthetic SAG1 peptides toT. gondii-specific CD8+CTL also was assayed. The present study found a high correlation between the binding ability of synthetic SAG1 peptides to HLA-A2 and the antigenicity of peptides toT. gondii-infected cell-specific CD8+CTL. |
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