Meng Qinglin, Zhang Binbin, Zhang Chun
Suzhou Municipal Key Laboratory of Molecular Diagnostics and Therapeutics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, Jiangsu, China.
Sheng Wu Gong Cheng Xue Bao. 2013 Feb;29(2):235-42.
Adeno-associated virus (AAV) has many advantages for gene therapy over other vector systems. However, after the production of recombinant AAV (Raav) vectors, the biological titration of rAAV stocks is still cumbersome. Different investigators used laboratory-specific methods or internal reference standards that may limit preclinical and clinical applications. The inverted terminal repeats (ITR) sequences are the only cis-regulated viral elements required for rAAV packaging and remain within viral vector genomes. ITR is the excellent target sequences for qPCR quantification of rAAV titer. In this study, we developed a novel qPCR strategy to quantify rAAVs' vector genome titer via targeting the ITR2 or ITR2-CMV element. In conclusion, the method is fast and accurate for the titration of rAAV2-derived vector genomes. It will promote the standardization of rAAV titration in the future.
与其他载体系统相比,腺相关病毒(AAV)在基因治疗方面具有许多优势。然而,在生产重组AAV(rAAV)载体后,rAAV储备液的生物学滴定仍然很繁琐。不同的研究人员使用特定实验室的方法或内部参考标准,这可能会限制临床前和临床应用。反向末端重复序列(ITR)是rAAV包装所需的唯一顺式调控病毒元件,并保留在病毒载体基因组内。ITR是用于qPCR定量rAAV滴度的优良靶序列。在本研究中,我们开发了一种新型qPCR策略,通过靶向ITR2或ITR2-CMV元件来定量rAAV的载体基因组滴度。总之,该方法对于滴定rAAV2衍生的载体基因组快速且准确。它将促进未来rAAV滴定的标准化。