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Elucidation of the pathophysiology of Langerhans cell histiocytosis by chemokine analysis

Research Project

Project/Area Number 25461606
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Pediatrics
Research InstitutionJichi Medical University

Principal Investigator

Morimoto Akira  自治医科大学, 医学部, 教授 (30326227)

Co-Investigator(Kenkyū-buntansha) 川原 勇太  自治医科大学, 医学部, 助教 (10570385)
塩田 曜子  国立研究開発法人国立成育医療研究センター, 小児がんセンター, 医師 (30307532)
早瀬 朋美  自治医科大学, 医学部, 助教 (50433587)
八木 正樹  自治医科大学, 医学部, 研究員 (60570398)
新島 瞳 (松本瞳 / 松本 瞳 / 新島 瞳(松本瞳))  自治医科大学, 医学部, 助教 (70598937)
翁 由紀子  自治医科大学, 医学部, 助教 (30438650)
Project Period (FY) 2013-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsランゲルハンス細胞組織球症 / ケモカイン / osteopontin / 破骨細胞様巨細胞 / 遺伝子多型 / サイトカイン / 多型性
Outline of Final Research Achievements

The serum levels of IL-9, IL-10, IL-15 and MIF in patients with Langerhans cell histiocytosis (LCH) were significantly high compared to those in Control. The serum levels of M-CSF and CCL 2 in patients with multisystem (MS) type LCH were significantly high compared to those in patients with single-system (SS) type LCH, while the serum levels of IL-18 and osteopontin (OPN) in patients with risk organ involvement (RO) positive MS type LCH were significantly high compared to those in patients with RO negative MS type LCH.
OPN was revealed to be essential for differentiation from immature dendritic cells to osteoclast-like giant cells.
In 48 LCH patients, OPN gene polymorphisms (rs9138, rs4754, rs11730582, rs1126772, rs1126616) were analyzed. No significant difference was identified in allele frequencies of these sites between LCH patients and controls, patients diagnosed under 2-years-old and over 2-years-old, patients with MS type and SS type, patients with MS-RO (+)and MS-RO (-).

Report

(5 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (10 results)

All 2017 2016 2015 2014

All Journal Article (10 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 10 results,  Acknowledgement Compliant: 2 results,  Open Access: 3 results)

  • [Journal Article] CNS-directed Prophylactic Approach to Langerhans Cell Histiocytosis.2017

    • Author(s)
      Imashuku S, Shioda Y, Morimoto A.
    • Journal Title

      J Pediatr Hematol Oncol.

      Volume: 39 Issue: 4 Pages: 321-322

    • DOI

      10.1097/mph.0000000000000781

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Intensified and prolonged therapy comprising cytarabine, vincristine and prednisolone improves outcome in patients with multisystem Langerhans cell histiocytosis: results of the Japan Langerhans Cell Histiocytosis Study Group-02 Protocol Study.2016

    • Author(s)
      Morimoto A, Shioda Y, Imamura T, Kudo K, Kawaguchi H, Sakashita K, Yasui M, Koga Y, Kobayashi R, Ishii E, Fujimoto J, Horibe K, Bessho F, Tsunematsu Y, Imashuku S.
    • Journal Title

      Int J Hematol.

      Volume: 104 Issue: 1 Pages: 99-109

    • DOI

      10.1007/s12185-016-1993-3

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Unique clonal relationship between T-cell acute lymphoblastic leukemia and subsequent Langerhans cell histiocytosis with TCR rearrangement and NOTCH1 mutation.2015

    • Author(s)
      Yokokawa Y, Taki T, Akiyama M, Kobayashi S, Nagoshi H, Chinen Y, Morimoto A, Ida H, Taniwaki M.
    • Journal Title

      Genes Chromosomes Cancer

      Volume: 54 Issue: 7 Pages: 409-417

    • DOI

      10.1002/gcc.22252

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics2015

    • Author(s)
      Murakami I, Oh Y, Morimoto A, Sano H, Kanzaki S, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Nagata K, Hayashi K, Imashuku S, Gogusev J, Jaubert F, Oka T, Yoshino T.
    • Journal Title

      Clin Proteomics.

      Volume: 12 Issue: 1 Pages: 16-16

    • DOI

      10.1186/s12014-015-9089-2

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Follow-up of pediatric patients treated by IVIG for Langerhans cell histiocytosis (LCH)-related neurodegenerative CNS disease.2015

    • Author(s)
      Imashuku S, Fujita N, Shioda Y, Noma H, Seto S, Minato T, Sakashita K, Ito N, Kobayashi R, Morimoto A
    • Journal Title

      Int J Hematol

      Volume: 101 Issue: 2 Pages: 191-197

    • DOI

      10.1007/s12185-014-1717-5

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Journal Article] Interleukin-1 loop model for pathogenesis of Langerhans cell histiocytosis2015

    • Author(s)
      Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Nagata K, Horie Y, Hayashi K, Imamura T, Morimoto A, Imashuku S, Gogusev J, Jaubert F, Takata K, Oka T, Yoshino T.
    • Journal Title

      Cell Commun Signal

      Volume: 13 Issue: 1 Pages: 13-13

    • DOI

      10.1186/s12964-015-0092-z

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Merkel cell polyomavirus DNA sequences in peripheral blood and tissues from patients with Langerhans cell histiocytosis.2014

    • Author(s)
      Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Horie Y, Hayashi K, Imamura T, Morimoto A, Imashuku S, Gogusev J, Jaubert F, Takata K, Oka T, Yoshino T.
    • Journal Title

      Hum Pathol.

      Volume: 45 Issue: 1 Pages: 119-126

    • DOI

      10.1016/j.humpath.2013.05.028

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Journal Article] High serum osteopontin levels in pediatric patients with high risk Langerhans cell histiocytosis.2014

    • Author(s)
      Oh Y, Morimoto A, Shioda Y, Imamura T, Kudo K, Imashuku S
    • Journal Title

      Cytokine

      Volume: 70 Issue: 2 Pages: 194-197

    • DOI

      10.1016/j.cyto.2014.07.002

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Osteopontin has a crucial role in osteoclast-like multinucleated giant cell formation2014

    • Author(s)
      Oh Yukiko, Oh Iekuni
    • Journal Title

      Journal of cellular biochemistry

      Volume: 115 Issue: 3 Pages: 585-95

    • DOI

      10.1002/jcb.24695

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Recent advances in Langerhans cell histiocytosis.2014

    • Author(s)
      Morimoto A, Oh Y, Shioda Y, Kudo K, Imamura T.
    • Journal Title

      Pediatr Int

      Volume: 56 Issue: 4 Pages: 451-461

    • DOI

      10.1111/ped.12380

    • Related Report
      2014 Research-status Report
    • Peer Reviewed

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Published: 2014-07-25   Modified: 2019-07-29  

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