Flotte Terence R, Brantly Mark L, Spencer L Terry, Byrne Barry J, Spencer Carolyn T, Baker Dawn J, Humphries Margaret
Department of Pediatrics, University of Florida, Gainesville, USA.
Hum Gene Ther. 2004 Jan;15(1):93-128. doi: 10.1089/10430340460732490.
A recombinant virus vector constructed from adeno-associated virus (AAV) that has been altered to carry the human alpha1-antitrypsin (hAAT) gene expressed from a hybrid chicken beta-actin promoter with a cytomegalovirus enhancer has been developed. The construct has been shown to initiate the production of hAAT in animal models closely matching the proposed human trial. The proposed clinical trial is an open-label, phase I study administering recombinant adeno-associated virus alpha1-antitrypsin (rAAV2-CB-hAAT) gene vector intramuscularly to AAT-deficient human subjects where gene expression can be measured directly in blood samples to assess safety. Safety parameters will be measurement of changes in serum chemistries and hematology, urinalysis, pulmonary function testing, semen assay for vector genomes, immunologic response to AAT, and AAV, as well as reported subject history of any symptoms.
一种由腺相关病毒(AAV)构建的重组病毒载体已被开发出来,该病毒载体经过改造,携带从具有巨细胞病毒增强子的杂交鸡β-肌动蛋白启动子表达的人α1-抗胰蛋白酶(hAAT)基因。在与拟进行的人体试验密切匹配的动物模型中,该构建体已被证明能启动hAAT的产生。拟进行的临床试验是一项开放标签的I期研究,将重组腺相关病毒α1-抗胰蛋白酶(rAAV2-CB-hAAT)基因载体肌肉注射给AAT缺乏的人类受试者,在那里可以直接在血样中测量基因表达以评估安全性。安全参数将包括血清化学和血液学变化的测量、尿液分析、肺功能测试、载体基因组的精液检测、对AAT和AAV的免疫反应,以及报告的任何症状的受试者病史。