Adenovirus-mediated in vivo gene transfer rapidly protects ornithine transcarbamylase-deficient mice from an ammonium challenge

被引:31
作者
Ye, XH
Robinson, MB
Pabin, C
Quinn, T
Jawad, A
Wilson, JM
Batshaw, ML
机构
[1] UNIV PENN,HLTH SYST & WISTAR INST,INST HUMAN GENE THERAPY,PHILADELPHIA,PA 19104
[2] UNIV PENN,HLTH SYST & WISTAR INST,DEPT MOL & CELLULAR ENGN,PHILADELPHIA,PA 19104
[3] UNIV PENN,HLTH SYST & WISTAR INST,DEPT MED,PHILADELPHIA,PA 19104
[4] CHILDRENS HOSP,DEPT PHARMACOL,PHILADELPHIA,PA 19104
[5] CHILDRENS HOSP,DEPT PEDIAT,PHILADELPHIA,PA
[6] UNIV PENN,CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
[7] CHILDRENS HOSP,DEPT GEN & THORAC SURG,PHILADELPHIA,PA 19104
[8] CHILDRENS HOSP,DEPT PEDIAT,DIV BIOSTAT & EPIDEMIOL,PHILADELPHIA,PA 19104
[9] UNIV PENN,PHILADELPHIA,PA 19104
关键词
D O I
10.1203/00006450-199704000-00012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The purpose of this study was to determine the time of onset, duration, and the efficacy of in vivo gene transfer in protecting the ornithine transcarbamylase deficient spf/Y mouse from an acute ammonium challenge. The animals were challenged with ammonia (10 mmol/kg NH4Cl) 1, 2, 7, 14, or 28 d after the administration of a recombinant adenoviral construct deleted in El and with a temperature sensitive mutation in E2. Although there was no protection with the control LacZ virus, the ornithine transcarbamylase (OTC)-containing vector provided partial protection from both behavioral symptoms (ataxia, seizures, and abnormal response to sound) and biochemical abnormalities (ammonium, aspartate, alanine, and glutamine) within 24 h and complete protection by 48 h. Mortality was also decreased. Animals receiving the vector 7 and 14 d before the ammonium load were also protected, whereas those treated 28 d before the challenge were not. OTC enzyme activity in liver of untreated spf/Y mice was 5% of control C3H mice. After gene transfer, activity was increased to near control levels through 14 d but had returned to baseline by 28 d. These studies indicate that adenovirus-mediated gene transfer confers a metabolic benefit within 24 h of administration and provides protection against an acute metabolic insult for at least 2 wk.
引用
收藏
页码:527 / 534
页数:8
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