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Development of a novel treatment of rhumatoid arthritis by inhibition of angiogenesis

Research Project

Project/Area Number 26461472
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Collagenous pathology/Allergology
Research InstitutionJuntendo University

Principal Investigator

NOZAWA Kazuhisa  順天堂大学, 医学部, 准教授 (30398680)

Research Collaborator HIRUMA Kaori  順天堂大学, 医学部, 大学院生
MATSUKI Yuko  順天堂大学, 医学部, 大学院生
KAJIWARA Mao  順天堂大学, 医学部, 実験助手
Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
KeywordsCTGF / 関節リウマチ / 血管新生 / 生物学的製剤 / Notch-1 / Angiogenesis / HUVEC / Rheumatoid arthritis
Outline of Final Research Achievements

We found that treatment with anti-CTGF antibodies, which have been already used for clinical trials for patients with pulmonary fibrosis and are ready for clinical trial for patients with rheumatoid arthritis (RA), prevented the development of arthritis in collagen induced arthritis (CIA) mice in vivo. Moreover, we found that CTGF promoted angiogenesis to human umbilical vascular endothelial cells (HUVEC) in vitro. Although angiogenesis in one of important factors for pathogenesis of RA, biologics for direct inhibition of angiogenesis is not available for the treatment of RA. Therefore, CTGF is involved in the important therapeutic target of RA and the treatment with biologics aiming inhibition of CTGF pathway can be considered as a useful treatment of RA.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (5 results)

All 2016 2015

All Journal Article (2 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 2 results,  Open Access: 2 results) Presentation (3 results)

  • [Journal Article] Antibodies to microtubule-associated protein-2 in the cerebrospinal fluid are a useful diagnostic biomarker for neuropsychiatric systemic lupus erythematosus.2016

    • Author(s)
      Yamada Y, Nozawa K, Nakano S, Mitsuo Y, Hiruma K, Doe K, Sekigawa I, Yamanaka K, Takasaki Y.
    • Journal Title

      Mod Rheumatol

      Volume: 16 Pages: 1-7

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Second-to-fourth Digit Ratio in Systemic Lupus Erythematosus2015

    • Author(s)
      Doe K, Nozawa K, Hirai T, Tsushima H, Hayashi E, Hiruma K, Ando S, Nakano S,
    • Journal Title

      J Rheumatol

      Volume: 42 Pages: 826-828

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] 抗リン脂質抗体がSLEの病型に与える影響について2015

    • Author(s)
      山田祐介、野澤和久、天野浩文、関川巌、髙崎芳成
    • Organizer
      日本臨床リウマチ学会
    • Place of Presentation
      兵庫県 神戸市
    • Year and Date
      2015-11-22
    • Related Report
      2015 Research-status Report
  • [Presentation] 抗リン脂質抗体がSLEの病型に与える影響について2015

    • Author(s)
      山田祐介、野澤和久、天野浩文、関川巌、髙崎芳成
    • Organizer
      日本リウマチ学会
    • Place of Presentation
      愛知県 名古屋市
    • Year and Date
      2015-04-23
    • Related Report
      2015 Research-status Report
  • [Presentation] 中枢神経ループスに対する新規バイオマーカーである脳脊髄液中 抗Microtubule-Associated Protein 2 抗体について2015

    • Author(s)
      山田祐介、野澤和久、天野浩文、関川巌、髙崎芳成
    • Organizer
      日本内科学会
    • Place of Presentation
      京都府 京都市
    • Year and Date
      2015-04-10
    • Related Report
      2015 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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