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)
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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Keywords | マラリア / 赤芽球 / CD8T細胞 / マクロファージ / 免疫 / Fas / フォスファチジルセリン / Plasmodium / CD8T細胞 |
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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Report
(3 results)
Research Products
(6 results)
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[Journal Article] Plasmodium berghei ANKA causes intestinal malaria associated with dysbiosis2015
Author(s)
Taniguchi T, Miyauchi E, Nakamura S, Hirai M, Suzue K, Imai T, Nomura T, Handa T, Okada H, Shimokawa C, Onishi R, Olia A, Hirata J, Tomita H, Ohno H, Horii T, Hisaeda H
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Journal Title
Scientific Reports
Volume: 5:15699
Issue: 1
Pages: 1-12
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
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