Moullier Philippe, Snyder Richard O
INSERM UMR 649, CHU Hôtel Dieu, Nantes, France.
Methods Enzymol. 2012;507:297-311. doi: 10.1016/B978-0-12-386509-0.00015-6.
Reference standard materials (RSMs) exist for a variety of biologics including vaccines but are not readily available for gene therapy vectors. To date, a recombinant adeno-associated virus serotype 2 RSM (rAAV2 RSM) has been produced and characterized and was made available to the scientific community in 2010. In addition, a rAAV8 RSM has been produced and will be characterized in the coming months. The use of these reference materials by members of the gene therapy field facilitates the calibration of individual laboratory vector-specific internal standards and the eventual comparison of preclinical and clinical data based on common dosage units. Normalization of data to determine therapeutic dose ranges of rAAV vectors for each particular tissue target and disease indication is important information that can enhance the safety and protection of patients.
包括疫苗在内的多种生物制品都有参考标准物质(RSM),但基因治疗载体的参考标准物质却难以获得。到目前为止,重组腺相关病毒2型参考标准物质(rAAV2 RSM)已制备并进行了特性鉴定,并于2010年提供给科学界。此外,rAAV8参考标准物质也已制备完成,并将在未来几个月内进行特性鉴定。基因治疗领域的成员使用这些参考物质有助于校准各个实验室载体特异性内标,并最终基于通用剂量单位比较临床前和临床数据。将数据标准化以确定针对每个特定组织靶点和疾病适应症的rAAV载体治疗剂量范围,是重要信息,可提高患者的安全性和保护水平。