2015 Fiscal Year Final Research Report
Analysis of the mechanisms of pathogenesis and eradication response in Helicobacter pylori-associated immune thrombocytopenia
Project/Area Number |
26870561
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Hematology
Laboratory medicine
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Research Institution | Kitasato University |
Principal Investigator |
SATOH Takashi 北里大学, 医療衛生学部, 講師 (90407114)
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Keywords | 免疫性血小板減少症 / Helicobacter pylori |
Outline of Final Research Achievements |
In this study, the associations between gene polymorphisms and rates of Helicobacter pylori (H. pylori) eradication response in patients with H.pylori-associated immune thrombocytopenia (ITP) were evaluated. Patients with ITP who were carriers of the FcγRIIB 232T or TGF-β -509T polymorphisms had significantly higher rates of H. pylori eradication responses than non-carriers. The frequency of the circulating anti-glycoprotein IIb/IIIa antibody-producing cells was significantly higher in patients with ITP that carried the FcγRIIB 232T allele than in those with the non-T allele. In addition, patients with ITP that carried the TGF-β -509T allele tended to have lower TGF-β levels. These findings suggest that FcγRIIB 232I/T and TGF-β -509C/T gene polymorphisms contribute to the susceptibility of H.pylori-associated ITP by controlling the autoimmune responses.
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Free Research Field |
血液検査学
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