Project/Area Number |
15K15379
|
Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
Allocation Type | Multi-year Fund |
Research Field |
Infectious disease medicine
|
Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
Negi Mariko 東京医科歯科大学, 大学院医歯学総合研究科, 助教 (70646108)
|
Co-Investigator(Kenkyū-buntansha) |
江石 義信 東京医科歯科大学, 大学院医歯学総合研究科, 教授 (70151959)
|
Research Collaborator |
KAKEGAWA Tomoya
OGAWA Tomohisa
|
Project Period (FY) |
2015-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
|
Keywords | 血中免疫複合体 / 溶連菌 / 急性糸球体腎炎 / モノクローナル抗体 / ポリクローナル抗体 |
Outline of Final Research Achievements |
In this study, we aimed to establish a new detection method for the antigens derived from streptococcus forming immune complexes in peripheral blood, which is considered to be involved in the onset of poststreptococcal acute glomerulonephritis. To develop a detection system, we attempted to product a monoclonal antibody to the streptococcus, but we have not yet obtained useful antibodies so far. We continue to create better monoclonal antibodies by devising immunogens now. On the other hand, we measured antibody titer against streptococcus using human serum from patients with glomerulonephritis. As results, IgG and IgA showed higher titer in the samples from IgA nephropathy patients than the samples from healthy persons. We have already established this detection method from our research on sarcoidosis, so this method can be applied to the samples with using IgA nephropathy if useful antibodies are available.
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