2015 Fiscal Year Final Research Report
Mechanism of protective immunity against malaria parasite parasitized erhtroblasts
Project/Area Number |
26860276
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Parasitology (including sanitary zoology)
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Research Institution | Gunma University |
Principal Investigator |
Imai Takashi 群馬大学, 医学(系)研究科(研究院), 助教 (10513434)
|
Project Period (FY) |
2014-04-01 – 2016-03-31
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Keywords | マラリア / 赤芽球 / CD8T細胞 / マクロファージ |
Outline of Final Research Achievements |
We recently discovered that mouse malaria parasites can parsitize erythroblasts which is the precursor of the RBC.Parasitized erythroblast express MHC class I and CD8 T cells recognized them an antigen-specific manner. In this study, we found that CD8 T cells are important to protection against parasitized eryhthroblast. FasL on CD8 T cells interacts with Fas (death receptor) on the parasitized erythroblasts and induces externalization of phosphatidylserine (PS). PS externalized infected cell are phagocytized by macrophage though Tim-4.
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Free Research Field |
寄生虫学
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