Laborda Eduardo, Puig-Saus Cristina, Cascalló Manel, Chillón Miguel, Alemany Ramon
1 Translational Research Laboratory, IDIBELL-Institut Català d'Oncologia , L'Hospitalet de Llobregat, 08907 Barcelona, Spain .
Hum Gene Ther Methods. 2013 Dec;24(6):372-80. doi: 10.1089/hgtb.2013.124. Epub 2013 Oct 8.
The contamination of adenovirus (Ad) stocks with adeno-associated viruses (AAV) is usually unnoticed, and it has been associated with lower Ad yields upon large-scale production. During Ad propagation, AAV contamination needs to be detected routinely by polymerase chain reaction without symptomatic suspicion. In this study, we describe that the coinfection of either Ad wild type 5 or oncolytic Ad with AAV results in a large-plaque phenotype associated with an accelerated release of Ad from coinfected cells. This accelerated release was accompanied with the expected decrease in Ad yields in two out of three cell lines tested. Despite this lower Ad yield, coinfection with AAV accelerated cell death and enhanced the cytotoxicity mediated by Ad propagation. Intratumoral coinjection of Ad and AAV in two xenograft tumor models improved antitumor activity and mouse survival. Therefore, we conclude that accidental or intentional AAV coinfection has important implications for Ad-mediated virotherapy.
腺病毒(Ad)储备液被腺相关病毒(AAV)污染通常不易被察觉,并且与大规模生产时较低的Ad产量有关。在Ad繁殖过程中,需要通过聚合酶链反应常规检测AAV污染,而无需有症状怀疑。在本研究中,我们描述了Ad野生型5或溶瘤性Ad与AAV的共感染会导致大斑块表型,这与Ad从共感染细胞中加速释放有关。在测试的三个细胞系中的两个中,这种加速释放伴随着Ad产量的预期下降。尽管Ad产量较低,但与AAV的共感染加速了细胞死亡并增强了由Ad繁殖介导的细胞毒性。在两个异种移植肿瘤模型中瘤内共注射Ad和AAV提高了抗肿瘤活性并延长了小鼠存活时间。因此,我们得出结论,意外或有意的AAV共感染对Ad介导的病毒疗法具有重要意义。