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Investigation on the role of microbiota and regulatory T cells on allregic airway inflammation

Research Project

Project/Area Number 23791104
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field 膠原病・アレルギー・感染症内科学
Research InstitutionThe University of Tokyo

Principal Investigator

HARADA Hiroaki  東京大学, 医学部附属病院, 助教 (40579687)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywordsアレルギー学
Research Abstract

We could not prove the hypothesis that microbiota could induce regulatory T cells and suppress allergic airway inflammation. Transcription factor Blimp-1 is thought to be implicated in the regulatory function of LAG3+Tregs, which is recently proposed as a novel regulatory T cell subcet. We showed that Blimp-1 expression of T cells enhanced eosiophil infiltration and suppressed lymphocyte infiltration and collagen deposition in mice with allergic airway inflammation. Our study indicates that LA3+Tregs are involved in the pathogenesis of allergic airway inflammation.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report

URL: 

Published: 2011-08-05   Modified: 2019-07-29  

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