Maxwell I H, Maxwell F, Schaack J
Department of Dermatology, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
J Virol. 1998 Oct;72(10):8371-3. doi: 10.1128/JVI.72.10.8371-8373.1998.
Production of recombinant adeno-associated virus (rAAV) requires helper functions that have routinely been provided by infection of the producer cells with adenovirus. Complete removal and/or inactivation of progeny adenovirus, present in such rAAV preparations, presents significant difficulty. Here, we report that an adenovirus type 5 (Ad5) mutant with the preterminal protein (pTP) gene deleted can provide helper function for the growth of rAAV. At high multiplicity, Ad5dl308DeltapTP was as efficient as the phenotypically wild-type Ad5dl309 in permitting growth of rAAV. Use of Ad5dl308DeltapTP, which is incapable of replication in the absence of complementation for pTP, as a helper avoids the need to remove contaminating adenovirus infectious activity by heat inactivation or by purification. Comparison of the transducing ability of rAAV generated with either Ad5dl308DeltapTP or Ad5dl309 as a helper demonstrated that the heat inactivation protocol generally used does not remove all of the helper Ad5dl309 function.
重组腺相关病毒(rAAV)的生产需要辅助功能,传统上是通过用腺病毒感染生产细胞来提供这些功能。彻底去除和/或灭活此类rAAV制剂中存在的子代腺病毒存在很大困难。在此,我们报告一种缺失前末端蛋白(pTP)基因的5型腺病毒(Ad5)突变体可为rAAV的生长提供辅助功能。在高感染复数下,Ad5dl308DeltapTP在允许rAAV生长方面与表型野生型Ad5dl309一样有效。使用在没有pTP互补的情况下无法复制的Ad5dl308DeltapTP作为辅助物,避免了通过热灭活或纯化去除污染腺病毒感染活性的需要。比较以Ad5dl308DeltapTP或Ad5dl309作为辅助物产生的rAAV的转导能力表明,通常使用的热灭活方案并不能去除所有的辅助Ad5dl309功能。