Raper S E, Wilson J M, Yudkoff M, Robinson M B, Ye X, Batshaw M L
Department of Surgery, University of Pennsylvania School of Medicine, Philadelphia, USA.
J Inherit Metab Dis. 1998;21 Suppl 1:119-37. doi: 10.1023/a:1005369926784.
There are a number of reasons for choosing ornithine transcarbamylase (OTC) deficiency as a candidate for gene therapy: the gene has been cloned; the disorder is relatively common; the current clinical outcome is poor; and there are authentic animal models. In considering the development of gene therapy for OTC deficiency, we focused on the use of in vivo gene therapy with an adenoviral vector. Using the partially OTC-deficient sparse fur mouse we found transduction and expression could be achieved using an intravenous infusion of a recombinant adenovirus containing the OTC cDNA. The results were transient as a result of immune activation in response to the vector and vector-transduced cells. By modifying the adenoviral construct, creating an E1 deletion-E2 temperature-sensitive mutation, we blunted the cytotoxic T lymphocyte immune response and achieved correction of biochemical abnormalities for 2-3 months. We also found that transduction and expression following gene transfer occurred sufficiently rapidly to protect against acute hyperammonaemia within 24 h. Subsequent preclinical studies in mice and non-human primates demonstrated that E1-E4-deleted vectors had a substantially improved safety profile and similar efficacy. With this evidence of efficacy and safety of adenoviral vectors, we are embarking on a phase I trial of intravascular gene transfer using an E1-E4-deleted vector in adults with partial OTC deficiency.
选择鸟氨酸转氨甲酰酶(OTC)缺乏症作为基因治疗候选对象有多个原因:该基因已被克隆;该疾病相对常见;目前的临床疗效不佳;并且存在可靠的动物模型。在考虑开发针对OTC缺乏症的基因治疗时,我们专注于使用腺病毒载体进行体内基因治疗。利用部分OTC缺乏的稀毛小鼠,我们发现通过静脉输注含OTC cDNA的重组腺病毒可实现转导和表达。由于对载体和载体转导细胞的免疫激活,结果是短暂的。通过修饰腺病毒构建体,产生E1缺失-E2温度敏感突变,我们减弱了细胞毒性T淋巴细胞免疫反应,并实现了2至3个月生化异常的纠正。我们还发现基因转移后的转导和表达足够迅速,可在24小时内预防急性高氨血症。随后在小鼠和非人类灵长类动物中的临床前研究表明,E1-E4缺失载体的安全性有了显著改善,且疗效相似。有了腺病毒载体疗效和安全性的这些证据,我们正着手对部分OTC缺乏的成年人进行使用E1-E4缺失载体的血管内基因转移的I期试验。