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AAV-ID: A Rapid and Robust Assay for Batch-to-Batch Consistency Evaluation of AAV Preparations

机译:AAV-ID:AAV制剂批次间一致性评估的快速而稳定的方法

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摘要

Adeno-associated virus (AAV) vectors are promising clinical candidates for therapeutic gene transfer, and a number of AAV-based drugs may emerge on the market over the coming years. To insure the consistency in efficacy and safety of any drug vial that reaches the patient, regulatory agencies require extensive characterization of the final product. Identity is a key characteristic of a therapeutic product, as it ensures its proper labeling and batch-to-batch consistency. Currently, there is no facile, fast, and robust characterization assay enabling to probe the identity of AAV products at the protein level. Here, we investigated whether the thermostability of AAV particles could inform us on the composition of vector preparations. AAV-ID, an assay based on differential scanning fluorimetry (DSF), was evaluated in two AAV research laboratories for specificity, sensitivity, and reproducibility, for six different serotypes (AAV1, 2, 5, 6.2, 8, and 9), using 67 randomly selected AAV preparations. In addition to enabling discrimination of AAV serotypes based on their melting temperatures, the obtained fluorescent fingerprints also provided information on sample homogeneity, particle concentration, and buffer composition. Our data support the use of AAV-ID as a reproducible, fast, and low-cost method to ensure batch-to-batch consistency in manufacturing facilities and academic laboratories.
机译:腺相关病毒(AAV)载体有望成为治疗性基因转移的临床候选药物,在未来几年中,许多基于AAV的药物可能会出现在市场上。为了确保到达患者的任何药水瓶在功效和安全性方面的一致性,监管机构要求对最终产品进行广泛的表征。身份是治疗产品的关键特征,因为它可以确保正确的标签和批次之间的一致性。当前,尚没有简便,快速和强大的表征分析能够在蛋白质水平上探查AAV产品的身份。在这里,我们调查了AAV颗粒的热稳定性是否可以告诉我们载体制剂的组成。 AAV-ID是一种基于差示扫描荧光法(DSF)的分析方法,在两个AAV研究实验室中针对六种不同的血清型(AAV1、2、5、6.2、8和9)进行了特异性,敏感性和重现性评估, 67种随机选择的AAV制剂。除了能够根据AAV血清型的解链温度对其进行区分外,获得的荧光指纹图谱还提供了有关样品均一性,颗粒浓度和缓冲液成分的信息。我们的数据支持使用AAV-ID作为可重现,快速且低成本的方法,以确保制造工厂和学术实验室之间的批次间一致性。

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