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岩藻糖苷酶缺乏症犬骨髓移植后临床疾病的改善

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

作者信息

Taylor R M, Farrow B R, Stewart G J

机构信息

Department of Veterinary Anatomy, University of Sydney, Australia.

出版信息

Am J Med Genet. 1992 Feb 15;42(4):628-32. doi: 10.1002/ajmg.1320420439.

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.

摘要

犬类岩藻糖苷贮积症作为神经内脏溶酶体贮积病治疗的动物模型进行了研究。在成功进行骨髓移植后,患有岩藻糖苷贮积症的犬类白细胞、血浆以及神经和内脏组织中的α-L-岩藻糖苷酶活性水平有所提高。酶活性的这种广泛增加伴随着岩藻糖苷贮积症外周神经和内脏病变的迅速改善以及中枢神经系统病理学的更逐渐改善。从小开始的长期移植降低了临床神经疾病的严重程度并减缓了其进展。临床症状出现后进行移植无效。这些发现表明,某些遗传性代谢紊乱,如岩藻糖苷贮积症所引起的神经损伤可能是可以预防的,但强调了早期诊断和治疗的必要性。

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