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苯丙酮尿症的基因治疗。

Gene therapy for phenylketonuria.

作者信息

Eisensmith R C, Woo S L

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Eur J Pediatr. 1996 Jul;155 Suppl 1:S16-9. doi: 10.1007/pl00014237.

Abstract

Classical phenylketonuria (PKU) is an autosomal recessive disorder caused by a deficiency of hepatic phenylalanine hydroxylase (PAH). Limitations of the current dietary treatment for PKU have led to the development of potential treatments based on somatic gene transfer. Three different vector systems have been examined. Vectors derived from a recombinant retrovirus or a DNA/protein complex can efficiently transduce the PAH cDNA into PAH-deficient hepatocytes in vitro, but the application of these vector systems is presently limited by their low transduction efficiency in vivo. In contrast, a vector derived from a recombinant adenovirus can restore 10%-80% of normal hepatic PAH activity into PAH-deficient mice, which completely normalizes serum phenylalanine levels. This treatment is transient and cannot be effectively re-administered due to the presence of neutralizing antibodies directed against the recombinant adenoviral vector. However, these findings suggest that PKU can be completely corrected by somatic gene therapy, and provide some direction for the future development of adenoviral vectors.

摘要

经典型苯丙酮尿症(PKU)是一种常染色体隐性疾病,由肝脏苯丙氨酸羟化酶(PAH)缺乏引起。目前PKU饮食治疗的局限性促使了基于体细胞基因转移的潜在治疗方法的发展。已对三种不同的载体系统进行了研究。源自重组逆转录病毒或DNA/蛋白质复合物的载体能够在体外有效地将PAH cDNA转导至PAH缺乏的肝细胞中,但目前这些载体系统的应用受到其在体内低转导效率的限制。相比之下,源自重组腺病毒的载体能够将10% - 80%的正常肝脏PAH活性恢复至PAH缺乏的小鼠体内,从而使血清苯丙氨酸水平完全正常化。这种治疗是短暂的,并且由于存在针对重组腺病毒载体的中和抗体而无法有效地再次给药。然而,这些发现表明PKU可通过体细胞基因治疗得到完全纠正,并为腺病毒载体的未来发展提供了一些方向。

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