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1998 Fiscal Year Final Research Report Summary

Gene therapy for neuronopathic Gaucher disease

Research Project

Project/Area Number 09670839
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionThe Jikei University School of Medicine

Principal Investigator

IDA H.  Jikei Univ., Dept.of Pediatrics assi prof., 医学部・小児科, 講師 (90167255)

Co-Investigator(Kenkyū-buntansha) ETO Y.  Jikei Univ., Dept.of Pediatrics prof., 医学部・小児科, 教授 (50056909)
HASEGAWA Y.  Jikei Univ., Dept.of Pediatrics senior investigator, 医学部・小児科, 助手 (60256435)
OHASHI T.  Jikei Univ., Dept.of Pediatrics assi prof., 医学部・小児科, 講師 (60160595)
OHNO T  Jikei Univ., Dept.of Microbiology prof., 医学部・微生物学第1, 教授 (60147288)
Project Period (FY) 1997 – 1998
KeywordsGaucher disease / Gene Tharapy / Adenovirus / Neurolipidosis / アデノウイルス / 動物モデル
Research Abstract

Gaucher disease (GD) is caused by deficiecy of activity of the enzyme glucocerebrosidase and consequent storage of the substrate glucocerebroside in cells of macrophage/monocyte lineage. Based on the presence and rate of progression of neurological symptoms, GD is classified into non-neuronopathic and neuronopathic forms. We investigated the methods to differenciate these two subtypes by mutation screening and to establish the treatment for neuronopathic GD.We studied mutation prevalence mong 47 unrelated Japanese patients with combination of PCR and SSCP.Eighty percent of total mutated alleles could be identified with this methods, however, it is impossible to distinguish non-neuronopathis from neuronopathic GD.Also we produced recombinant adenovirus that express human glucuronidase and this recombinant adenovirus to animal model intravenously. Pathological abnormalities in liver and spleen were improved, and the urinary glycosaminoglycans were also reduced in treated mice. Transduction of enzyme into brain was seen only by adminstration of direct injection of recombinant adenovirus into the lateral ventricles.

  • Research Products

    (16 results)

All Other

All Publications (16 results)

  • [Publications] Ida H, Eto Y, et al.: "Severa skeketal complications in Japanese patients with type 1 Gaucher disease." J Inher Matab Dis. 22. 63-73 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ida H, Rennert OM, et al.: "Type 1 Gaucher Disease : Phenotypic Expression and Natural History in Japanese Patients." Blood Cells, Molecules, and Disease. 24・5. 73-81 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Takahashi, H.Ida et al.: "Enzyme therapy in Gaucher disease type 2 : an autopsy case." Tohoku J Exp Med. 186. 143-149 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ohashi T, et al.: "Efficient and persistent expression of β-glucuronidase gene in CD34+ cells from human umbilical cord blood by retroviral vector." Eur J Haematol. 61. 235-239 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Ida, K.Maekawa, et al.: "Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease : identification of four novel mutations" J Inher Metab Dis. 20. 67-73 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] E.Uyama, H.Ida et al.: "D409H/D409H genotype in Gaucher -like disease" J Med Genet. 34. 175 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ida H., et al.: "Severa skeketal complications in Japanese patients with type 1 Gaucher disease." J Inher Matab Dis. 22. 63-73 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ida H., et al.: "Type 1 Gaucher disease : phenotypic expression and natural history in Japanese Gaucher disease." Blood Cells Mol and Dis. 24. 73-81 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takahashi T., Ida H., et al.: "Enzyme therapy in Gaucher disease type 2 : an autopsy case." Tohoku J Exp Med. 186. 143-149 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ohashi T., et al.: "Efficient and persistent expression of beta-glucuronidase gene in CD34+ cells from human umbilical cord blood by retroviral vector." Eur J Haematol. 61. 235-239 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yokoo T,Ohashi T,et al.: "Inflamed site-specific gene delivery using bone marrow-derived CD11b+CD18+ Vehicle cells in mice." Hum.Gene Ther.9. 17381-17388 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kurosawa K., Eto Y.et al.: "Prevalence of arylsulphatase A mutations in 11 Japanese patients with metachromatic leukodystrophy : Identification of two novel mutations." J.Inher.Metab.Dis.21. 781-782 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ida H., et al.: "Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease : identification of four novel mutations" J Inher Metab Dis. 20. 67-73 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] E.Uyama, H.Ida et al.: "D409H/D409H genotype in Gaucher-like disease" J Med Genet. 34. 175 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Ohashi et al.: "Adenoviral-mediated gene transfer and expression of human beta-glucuronidase gene in the liver, spleen, and central nervous system in MPS VII mice." Proc Natl Acad Sci USA. 94. 1287-1292 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Iwasawa K., Ida H.and Eto Y.: "Differences in origin of the 1448C mutation in patientswith Gaucher disease." Acta Pediatr.Jap.39. 451-453 (1997)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-12-08  

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