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2019 Fiscal Year Final Research Report

Inhibition of DC cells by HGF for immune tolerance induction in a mouse model of bone marrow allotransplantation

Research Project

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Project/Area Number 15K08402
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Experimental pathology
Research InstitutionOkayama University of Science (2018-2019)
Osaka University (2015-2017)

Principal Investigator

Mizuno Shinya  岡山理科大学, 理学部, 教授 (10219644)

Project Period (FY) 2015-04-01 – 2020-03-31
KeywordsHGF / c-Met / macrophages / immune response / cytokine storm
Outline of Final Research Achievements

Graft versus host disease is one of the most pathological events after bone marrow transplantation (BMT), with a clinical frequency of 30-50% among them. HGF is known to induce immunological tolerance in animal models of cardiac and renal transplantation, but it is still unclear how HGF acquires the tolerant responses at molecular levels. Thus, we used murine models of LPS- and BMT-induced inflammation to address the molecular basis of HGF-induced anti-immunological outcomes.
As a result, we found that blood HGF levels apparently increased in the murine models during systemic inflammation, associated with the increase in c-Met active levels in macrophages and possibly in DC cells. Importantly, HGF injection further enhanced the c-Met activation in these immunogenic cells, along with the decreased blood levels of inflammatory cytokines. In addition, we found that induction of IDO1 by HGF is, at least in part, responsible for the inhibitory effect of HGF on cytokine storm in vitro.

Free Research Field

実験病理学

Academic Significance and Societal Importance of the Research Achievements

BM後に発症するGVHDはサイトカインストーム(CS)に依存する。CSは活性化したMφやDC細胞が放出する炎症性サイトカインの過剰な反応によってもたらされる。一方、HO1やIDO1といったオキシゲナーゼは炎症病態や自己免疫疾患において免疫寛容をもたらす。今回の研究によりこのような病態ではHGFがMφ/DC細胞などの免疫指令細胞を直接標的とし、オキシゲナーゼの誘導を介してCS抑制と免疫寛容を促す可能性を見いだした。CSはGVHDのみならず敗血症や新型コロナウイルス感染症などでも問題視される共通病態であり、HGF補充療法がこのような疾患を制圧する可能性を示した上で大きなインパクトを持つ。

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Published: 2021-02-19  

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