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编码人肿瘤坏死因子受体-免疫球蛋白Fc融合基因的重组腺相关病毒2载体的临床前安全性评估

Preclinical safety evaluation of recombinant adeno-associated virus 2 vector encoding human tumor necrosis factor receptor-immunoglobulin Fc fusion gene.

作者信息

Zhou Xiaobing, Shen Lianzhong, Liu Li, Wang Chao, Qi Weihong, Zhao Aizhi, Wu Xiaobing, Li Bo

机构信息

a National Center for Safety Evaluation of Drugs, National Institutes of Food and Drug Control , Beijing , China.

b AGTC Gene Technology Company Ltd. , Beijing , China.

出版信息

Hum Vaccin Immunother. 2016 Mar 3;12(3):732-9. doi: 10.1080/21645515.2015.1090070.

Abstract

Recombinant adeno-associated virus (rAAV) 2 vector gene therapy offers promise for the healing of Rheumatoid arthritis. To support the clinical development of the candidate gene therapeutic product in China, a comprehensive preclinical safety assessment of rAAV2 encoding human TNF receptor-immunoglobulin Fc fusion gene (rAAV2/human TNFR:Fc), were conducted in 3 species of experimental animals. No abnormal findings were observed in mice following single intravenous administration with test article. Compared with the control group, no differences in mean body weight, food consumption in rats and monkeys following the repeated intraarticular administration with rAAV2/human TNFR:Fc. There were also no significant adverse effects due to treatment noted by clinical chemistry, hematology and pathology assessments. After intraarticular administration with rAAV2/human TNFR:Fc, the vector DNA initially distributed to spleen, lymph nodes, and joint synovium. The vector DNA cleared rapidly as it could be detected mainly at the site of injection by 91 d post-administration (182 d for monkey). Taken together, localized delivery of rAAV2/human TNFR:Fc showed no significant toxicity in mice, rats, and monkeys, which support the planned clinical evaluation of this product.

摘要

重组腺相关病毒(rAAV)2载体基因疗法为类风湿性关节炎的治愈带来了希望。为支持该候选基因治疗产品在中国的临床开发,对编码人肿瘤坏死因子受体-免疫球蛋白Fc融合基因的rAAV2(rAAV2/人TNFR:Fc)在3种实验动物中进行了全面的临床前安全性评估。单次静脉注射受试物后,在小鼠中未观察到异常发现。与对照组相比,rAAV2/人TNFR:Fc反复关节内给药后,大鼠和猴子的平均体重、食物消耗量无差异。临床化学、血液学和病理学评估也未发现因治疗导致的显著不良反应。关节内注射rAAV2/人TNFR:Fc后,载体DNA最初分布于脾脏、淋巴结和关节滑膜。载体DNA清除迅速,给药后91天(猴子为182天)主要在注射部位可检测到。综上所述,rAAV2/人TNFR:Fc的局部给药在小鼠、大鼠和猴子中未显示出显著毒性,这支持了该产品计划中的临床评估。

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