Literature DB >> 1609845

Amelioration of clinical disease following bone marrow transplantation in fucosidase-deficient dogs.

R M Taylor1, B R Farrow, G J Stewart.   

Abstract

Canine fucosidosis was studied as an animal model for the treatment of neurovisceral lysosomal storage disease. Following successful bone marrow engraftment, dogs with fucosidosis had increased levels of alpha-L-fucosidase enzyme activity in leukocytes, plasma, and neural and visceral tissues. This widespread increase in enzyme activity was accompanied by a rapid improvement in the peripheral nerve and visceral lesions of fucosidosis and a more gradual improvement in the central nervous system pathology. Long-term engraftment from an early age reduced the severity and slowed the progression of clinical neurological disease. Transplantation after the onset of clinical signs was not effective. These findings suggest that the neurological damage caused by some inherited metabolic disorders, such as fucosidosis, may be preventable but emphasise the need for early diagnosis and treatment.

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Year:  1992        PMID: 1609845     DOI: 10.1002/ajmg.1320420439

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  22 in total

1.  Delivering drugs to the central nervous system: an overview.

Authors:  Patricia I Dickson
Journal:  Drug Deliv Transl Res       Date:  2012-06       Impact factor: 4.617

2.  Possible beta-mannosidosis chimera. Altered expression of metabolic perturbations.

Authors:  M Z Jones; K T Cavanagh; R Kranich; C Traviss; Y Fujita; M Ohta; F Matsuura
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Secretion of phosphomannosyl-deficient arylsulphatase A and cathepsin D from isolated human macrophages.

Authors:  Nicole Muschol; Ulrich Matzner; Stephan Tiede; Volkmar Gieselmann; Kurt Ullrich; Thomas Braulke
Journal:  Biochem J       Date:  2002-12-15       Impact factor: 3.857

4.  Bone marrow transplantation does not ameliorate the neurologic symptoms in mice deficient in hypoxanthine guanine phosphoribosyl transferase (HPRT).

Authors:  B E Wojcik; H A Jinnah; C E Muller-Sieburg; T Friedmann
Journal:  Metab Brain Dis       Date:  1999-03       Impact factor: 3.584

5.  Murine mucopolysaccharidosis type VII: long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation.

Authors:  M S Sands; C Vogler; A Torrey; B Levy; B Gwynn; J Grubb; W S Sly; E H Birkenmeier
Journal:  J Clin Invest       Date:  1997-04-01       Impact factor: 14.808

Review 6.  Gene therapy for lysosomal storage diseases (LSDs) in large animal models.

Authors:  Mark Haskins
Journal:  ILAR J       Date:  2009

Review 7.  Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases.

Authors:  William Krivit
Journal:  Springer Semin Immunopathol       Date:  2004-09-25

8.  Five decades of progress in haematopoietic cell transplantation based on the preclinical canine model.

Authors:  M Lupu; R Storb
Journal:  Vet Comp Oncol       Date:  2007-03       Impact factor: 2.613

9.  Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotype.

Authors:  J J Hopwood; A Vellodi; H S Scott; C P Morris; T Litjens; P R Clements; D A Brooks; A Cooper; J E Wraith
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

10.  The molecular defect underlying canine fucosidosis.

Authors:  B J Skelly; D R Sargan; M E Herrtage; B G Winchester
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318

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