Department of Immunology, Genetics and Pathology; Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Methods Mol Biol. 2022;2521:249-258. doi: 10.1007/978-1-0716-2441-8_13.
Production of conditionally replicating adenoviruses may unfortunately generate undesired replication-competent adenovirus (RCA) which raises safety concerns in clinical usage. Cell-based assays can detect RCA in batches of nonreplicating adenoviral vectors but cannot distinguish RCA from conditionally replicating oncolytic adenoviruses. Considering the great potential in using oncolytic viruses for cancer treatment, there is a need for comprehensive RCA-detection and -quantification methods. Here, we present a quantitative polymerase chain reaction (qPCR)-based assay that can be used to detect RCA particles in batches of conditionally replicating oncolytic adenoviruses. The assay is quantifying RCA by detection of the specific DNA sequence generated after a recombination event. Results showed that the method can successfully detect low levels of RCA, with a low limit of detection of ten viral particles.
生产条件复制型腺病毒可能会产生不理想的复制型腺病毒(RCA),这在临床应用中引起了安全问题。基于细胞的检测方法可以在非复制型腺病毒载体的批次中检测 RCA,但不能区分 RCA 和条件复制型溶瘤腺病毒。考虑到溶瘤病毒在癌症治疗中的巨大潜力,需要全面的 RCA 检测和定量方法。在这里,我们提出了一种基于定量聚合酶链反应(qPCR)的检测方法,可用于检测条件复制型溶瘤腺病毒批次中的 RCA 颗粒。该检测方法通过检测重组事件后产生的特定 DNA 序列来定量 RCA。结果表明,该方法可以成功地检测到低水平的 RCA,检测下限为十个病毒颗粒。