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在先前接受腺病毒基因转移的鸟氨酸转氨甲酰酶缺乏症研究对象的肿瘤组织中未检测到载体序列。

Vector sequences are not detected in tumor tissue from research subjects with ornithine transcarbamylase deficiency who previously received adenovirus gene transfer.

机构信息

Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Hum Gene Ther. 2013 Sep;24(9):814-9. doi: 10.1089/hum.2013.118.

Abstract

A 66-year-old woman heterozygous for a mutation in the ornithine transcarbamylase gene (Otc) participated in a phase I gene therapy trial for OTC deficiency. She received an adenovirus (Ad) vector expressing the functional OTC gene by intraportal perfusion. Fourteen years later she developed and subsequently died of hepatocellular carcinoma. A second subject, a 45-year-old woman, enrolled in the same trial presented with colon cancer 15 years later. We sought to investigate a possible association between the development of a tumor and prior adenoviral gene transfer in these two subjects. We developed and validated a sensitive nested polymerase chain reaction assay for recovering recombinant Ad sequences from host tissues. Using this method, we could not detect any Ad vector DNA in either tumor or normal tissue from the two patients. Our results are informative in ruling out the possibility that the adenoviral vector might have contributed to the development of cancer in those two subjects.

摘要

一位 66 岁的女性杂合子携带鸟氨酸转氨甲酰酶基因(Otc)突变,参与了一项针对 OTC 缺乏症的 I 期基因治疗试验。她通过门静脉内灌注接受了表达功能性 Otc 基因的腺病毒(Ad)载体。14 年后,她患上了肝细胞癌并随后死亡。第二位受试者,一位 45 岁的女性,在同一项试验中患有结肠癌,15 年后去世。我们试图调查这两个患者的肿瘤发生与先前腺病毒基因转移之间是否存在关联。我们开发并验证了一种灵敏的巢式聚合酶链反应检测方法,用于从宿主组织中回收重组 Ad 序列。使用这种方法,我们无法在两个患者的任何肿瘤或正常组织中检测到任何腺病毒载体 DNA。我们的结果排除了腺病毒载体可能导致这两个患者癌症发展的可能性。

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