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A role of FcgRIIB in systemic sclerosis

Research Project

Project/Area Number 15K09762
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Dermatology
Research InstitutionKanazawa University

Principal Investigator

Hamaguchi Yasuhito  金沢大学, 医学系, 准教授 (60420329)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2015: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywords全身性強皮症 / FcγRIIB / B細胞
Outline of Final Research Achievements

We evaluated the expression of FcγRIIB on B cell subsets in systemic sclerosis (SSc). The expressions of FcγRIIB on SSc naïve B cells and double negative (DN) memory B cells were significantly elevated than that on B cells of healthy subjects. Patients with the elavated expression of FcγRIIB on DN memory B cells more frequently had interstitial lung disease than those with normal levels. In bleomycin-induced fibrosis model, fibrosis was singnificanlty worsened in FcγRIIB-deficient mice compared to wild-type mice. Our results suggest that SSc B cells exhibit compensatory increases in the expression of FcγRIIB in order to suppress the abnormal activation of B cells, and the expression of FcγRIIB may be an indicator of the clinical severity of SSc.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report

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Published: 2015-04-16   Modified: 2019-03-29  

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