Günzburg W, Mhashilkar A M, Hindi M
Institute of Molecular Virology, Gsf Munich, Ingolst Der Landstrasse 1, D-8042 Neuherberg, Germany.
Curr Opin Mol Ther. 1999 Oct;1(5):651-7.
Efficient inhibition of human immunodeficiency virus-1 (HIV-1) replication with intracellularly expressed antiviral genes would be an important step toward clinical gene therapy for HIV-1 disease. Enzo Biochem is investigating and developing antisense genes as a potential gene therapy approach against a variety of conditions including acquired immunodeficiency syndrome (AIDS), cancer and hepatitis. The subsidiary of Enzo Biochem, Enzo Therapeutics, utilized its StealthVector technology and initiated phase I trials in July 1998 [291511,307156]. StealthVector, which is comprised of independent antisense sequences directed against two functional HIV-1 regions, is involved in regulation of gene expression soon after HIV infection, transactivation response (TAR) and tat/rev. StealthVector localizes primarily in the cell nucleus, where it could be most effective in inhibiting viral growth.
利用细胞内表达的抗病毒基因有效抑制人类免疫缺陷病毒1型(HIV-1)复制,将是迈向HIV-1疾病临床基因治疗的重要一步。安佐生化公司正在研究和开发反义基因,作为针对包括获得性免疫缺陷综合征(艾滋病)、癌症和肝炎在内的多种病症的潜在基因治疗方法。安佐生化公司的子公司安佐治疗公司利用其StealthVector技术,并于1998年7月启动了I期试验[291511,307156]。StealthVector由针对两个功能性HIV-1区域的独立反义序列组成,在HIV感染后不久参与基因表达的调控,即反式激活应答(TAR)和tat/rev。StealthVector主要定位于细胞核,在那里它可能最有效地抑制病毒生长。