Mautino M R, Morgan R A
Clinical Gene Therapy Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-1851, USA.
Hum Gene Ther. 2000 Sep 20;11(14):2025-37. doi: 10.1089/10430340050143444.
We describe an HIV-based lentiviral vector that expresses a 1-kb antisense mRNA directed against the HIV-1 mRNAs containing env sequences. The expression of antisense env mRNAs (envAS) does not inhibit the synthesis of p24 expressed from the HIV-1 helper plasmid used to package the vector, as this helper has a deletion in the env gene. This allows the production of high-titer VSV-G pseudotyped lentiviral particles. In challenge experiments using unselected populations of SupT1 cells transduced with this vector, a complete inhibition of HIV-1 replication was observed for long periods of in vitro culture, even at high HIV-1 infectious doses. The potent inhibition of HIV-1 replication by this vector correlated with a low occurrence of mobilization of the vector to previously untransduced cells. The infectivity of the wild-type HIV-1 that escapes inhibition was highly inhibited, suggesting that the vector is providing HIV-1 inhibition of replication not only due to its antisense effect but also by competing for encapsidation and mobilization to noninfected cells.
我们描述了一种基于HIV的慢病毒载体,它表达一种针对含有env序列的HIV-1 mRNA的1 kb反义mRNA。反义env mRNA(envAS)的表达并不抑制从用于包装载体的HIV-1辅助质粒表达的p24的合成,因为该辅助质粒在env基因中有缺失。这使得能够生产高滴度的VSV-G假型慢病毒颗粒。在用该载体转导的未选择的SupT1细胞群体进行的挑战实验中,即使在高HIV-1感染剂量下,在长时间的体外培养中也观察到HIV-1复制被完全抑制。该载体对HIV-1复制的有效抑制与载体向先前未转导细胞的动员发生率低相关。逃脱抑制的野生型HIV-1的感染性受到高度抑制,这表明该载体不仅因其反义作用,还通过竞争包装和向未感染细胞的动员来抑制HIV-1复制。