Ding Zhaobing, Harding Cary O, Thöny Beat
Department of Pediatrics, University of Zürich, Steinwiesstrasse 75, CH-8032, Zürich, Switzerland.
Mol Genet Metab. 2004 Jan;81(1):3-8. doi: 10.1016/j.ymgme.2003.09.010.
Phenylketonuria (or PKU) is a well-known and widespread genetic disease for which many countries perform newborn screening, and life-long dietary restriction is still the ultimate and effective therapy. However, the diet is complicated, unpalatable, and expensive. The long-term effects of diet discontinuation in adults, except for the serious adverse effects of maternal hyperphenylalaninemia upon the developing fetus, have not been systematically studied, but cognitive decline and neurologic abnormalities have been anecdotally reported. Thus, alternative approaches for PKU therapy, including gene therapy, must be further explored. Here we summarize past present nonviral and viral gene transfer approaches, both in vitro studies and preclinical animal trials, to delivering the PAH gene into liver or other organs as potential alternatives to life-long phenylalanine-restricted dietary therapy.
苯丙酮尿症(PKU)是一种广为人知且普遍存在的遗传病,许多国家都对其进行新生儿筛查,终身饮食限制仍是最终有效的治疗方法。然而,这种饮食复杂、难吃且昂贵。除了母体高苯丙氨酸血症对发育中的胎儿有严重不良影响外,尚未对成人停止饮食的长期影响进行系统研究,但有零星报道称会出现认知能力下降和神经异常。因此,必须进一步探索苯丙酮尿症治疗的替代方法,包括基因治疗。在此,我们总结过去和现在的非病毒和病毒基因转移方法,包括体外研究和临床前动物试验,这些方法旨在将苯丙氨酸羟化酶(PAH)基因导入肝脏或其他器官,作为终身限制苯丙氨酸饮食治疗的潜在替代方法。