用 HEK293 哺乳动物细胞和 Sf9 昆虫细胞生产的 AAV 向量批次中残留 MicroRNA 的特征

IF 4.6 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Therapy-Methods & Clinical Development Pub Date : 2024-07-25 DOI:10.1016/j.omtm.2024.101305
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引用次数: 0

摘要

AAV 目前已进行了 130 多项临床试验,并有 8 种基因治疗产品获得批准,是在体内输送治疗 DNA 的最常用工具之一。对 AAV 批次进行分析的一个关键质量属性是是否存在残留 DNA,因为残留 DNA 可能会带来基因毒性风险或诱发免疫反应。令人惊讶的是,以前从未调查过细胞衍生的小 RNA(如微 RNA)的存在。在这项研究中,我们检测了在哺乳动物细胞或昆虫细胞中生产的纯化 AAV 批次中是否存在 miRNA。我们的研究结果表明,无论生产细胞系或囊壳血清型(2 和 8)如何,所有批次的 AAV 中都存在 miRNA。定量检测表明,miRNA 与 rAAV 颗粒共同纯化的比例与它们在生产细胞中的丰度相关。通过免疫亲和层析纯化过程(包括切向流过滤步骤)或 RNase 处理,残留 miRNA 的水平降低了,这表明大多数 miRNA 杂质可能是非包囊化的。总之,我们首次证明了 miRNA 可与 AAV 颗粒共同纯化。要确定这些 miRNA 是否会干扰 AAV 介导的基因治疗的安全性或疗效,还需要进一步的研究。
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Characterization of Residual MicroRNAs in AAV Vector Batches Produced in HEK293 Mammalian Cells and Sf9 Insect Cells

With more than 130 clinical trials and eight approved gene therapy products, AAVs stand as one of the most popular vehicles to deliver therapeutic DNA in vivo. One critical quality attribute analyzed in AAV batches is the presence of residual DNA, as it could pose genotoxic risks or induce immune responses. Surprisingly, the presence of small cell-derived RNAs, such as micro-RNAs, has not been previously investigated. In this study, we examined the presence of miRNAs in purified AAV batches produced in mammalian or in insect cells. Our findings revealed that miRNAs were present in all batches, regardless of the production cell line or capsid serotype (2 and 8). Quantitative assays indicated that miRNAs were co-purified with the rAAV particles in a proportion correlated with their abundance in the production cells. The level of residual miRNAs was reduced via an immunoaffinity chromatography purification process including a tangential flow filtration step or by RNase treatment, suggesting that most miRNA contaminants are likely non-encapsidated. In summary, we demonstrate, for the first time, that miRNAs are co-purified with AAV particles. Further investigations are required to determine whether these miRNAs could interfere with the safety or efficacy of AAV-mediated gene therapy.

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来源期刊
Molecular Therapy-Methods & Clinical Development
Molecular Therapy-Methods & Clinical Development Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.90
自引率
4.30%
发文量
163
审稿时长
12 weeks
期刊介绍: The aim of Molecular Therapy—Methods & Clinical Development is to build upon the success of Molecular Therapy in publishing important peer-reviewed methods and procedures, as well as translational advances in the broad array of fields under the molecular therapy umbrella. Topics of particular interest within the journal''s scope include: Gene vector engineering and production, Methods for targeted genome editing and engineering, Methods and technology development for cell reprogramming and directed differentiation of pluripotent cells, Methods for gene and cell vector delivery, Development of biomaterials and nanoparticles for applications in gene and cell therapy and regenerative medicine, Analysis of gene and cell vector biodistribution and tracking, Pharmacology/toxicology studies of new and next-generation vectors, Methods for cell isolation, engineering, culture, expansion, and transplantation, Cell processing, storage, and banking for therapeutic application, Preclinical and QC/QA assay development, Translational and clinical scale-up and Good Manufacturing procedures and process development, Clinical protocol development, Computational and bioinformatic methods for analysis, modeling, or visualization of biological data, Negotiating the regulatory approval process and obtaining such approval for clinical trials.
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