Title of article :
Preclinical safety evaluation of rAd5-hTERTC27 by intravenous injection
Author/Authors :
Yue، نويسنده , , Pei-jian and He، نويسنده , , Lei and Li، نويسنده , , Yi and Shen، نويسنده , , Qingyu and Li، نويسنده , , Mei and Huang، نويسنده , , Da-quan and Huang، نويسنده , , Jun-Jian and Peng، نويسنده , , Ying، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
10
From page :
53
To page :
62
Abstract :
The safety of rAd5-hTERTC27, a replication defective adenovirus vector carrying hTERTC27 for possible use against hepatocellular carcinoma (HCC) was assessed. In single-dose evaluations, intravenous dose levels of up to 2 × 1011 VP/kg in rats and 9 × 1010 VP/kg in monkeys were well tolerated with no abnormal changes in general signs, body weight and food consumption, and no significant differences in biochemical parameters, urinalysis, ECG, and systemic necropsy observations between the rAd5 groups and solvent control group except that slight hematological change was observed. No hemolytic effect using rabbit blood, local perivasculitis following intravenous injection in rabbits or systemic anaphylaxis in guinea pigs following intravenous dosing was seen. No effects on the central nervous system of mice occurred following intravenous dosing with the exception of an increase in sleep duration at the dose of 1.2 × 1011 VP/kg (p < 0.05) but not at lower doses of 2 × 1010 and 6 × 1010 VP/kg in the hypnotic synergism test. These results demonstrate that administration of rAd5-hTERTC27 was well tolerated in an initial set of safety studies as part of an evaluation to allow human trials for the treatment of HCC.
Keywords :
hTERTC27 , HCC , Gene Therapy , Single-dose toxicity , Preclinical evaluation
Journal title :
Regulatory Toxicology and Pharmacology
Serial Year :
2013
Journal title :
Regulatory Toxicology and Pharmacology
Record number :
1491809
Link To Document :
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