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一名鸟氨酸转氨甲酰酶缺乏患者在腺病毒基因转移后发生致命性全身炎症反应综合征。

Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer.

作者信息

Raper Steven E, Chirmule Narendra, Lee Frank S, Wivel Nelson A, Bagg Adam, Gao Guang-ping, Wilson James M, Batshaw Mark L

机构信息

Department of Surgery, University of Pennsylvania School of Medicine, BRB II/III Rm, 607 421 Curie Blvd, Philadelphia, PA 19104, USA.

出版信息

Mol Genet Metab. 2003 Sep-Oct;80(1-2):148-58. doi: 10.1016/j.ymgme.2003.08.016.

DOI:10.1016/j.ymgme.2003.08.016
PMID:14567964
Abstract

We report the death of an 18-year-old male with partial ornithine transcarbamylase (OTC) deficiency who participated in a pilot (safety) study of gene therapy. The vector used for this trial was based on human adenovirus type 5, deleted in E1 and E4, and contained human OTC cDNA. It was infused into the right hepatic artery at a dose of 6x10(11)particles/kg. Approximately 18 h. following gene transfer the subject was noted to have altered mental status and jaundice--clinical signs not seen in any of the first 17 subjects in this study. Subsequently, his clinical course was marked by systemic inflammatory response syndrome, biochemically detectable disseminated intravascular coagulation, and multiple organ system failure, leading to death 98 h following gene transfer. Post-mortem examination was consistent with the clinical course, and vector DNA sequences were readily detectable in most tissues. The subject had high serum levels of IL-6 and IL-10 but normal TNFalpha immediately after infusion of the vector. This experience points to the limitations of animal studies in predicting human responses, the steep toxicity curve for replication defective adenovirus vectors, substantial subject-to-subject variation in host responses to systemically administered vectors, and the need for further study of the immune response to these vectors.

摘要

我们报告了一名患有部分鸟氨酸转氨甲酰酶(OTC)缺乏症的18岁男性的死亡病例,该患者参与了一项基因治疗的试点(安全性)研究。用于该试验的载体基于5型人腺病毒,E1和E4区域缺失,并包含人OTC cDNA。以6×10¹¹颗粒/千克的剂量注入右肝动脉。基因转移后约18小时,发现该受试者精神状态改变和黄疸,这是本研究前17名受试者中均未出现的临床体征。随后,他的临床病程以全身炎症反应综合征、生化检测到的弥散性血管内凝血和多器官系统功能衰竭为特征,导致基因转移后98小时死亡。尸检结果与临床病程一致,并且在大多数组织中很容易检测到载体DNA序列。在注入载体后,该受试者血清IL-6和IL-10水平较高,但TNFα水平正常。这一事件表明动物研究在预测人类反应方面存在局限性,复制缺陷型腺病毒载体的毒性曲线陡峭,宿主对全身给药载体的反应存在很大的个体差异,以及需要进一步研究对这些载体的免疫反应。

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