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深入了解 AAV9 的降解途径。

Insight Into the Degradation Pathways of an AAV9.

机构信息

Biologics Drug Product Development, AbbVie Bioresearch Center, Worcester, MA 01605, United States.

Biotherapeutics and Genetic Medicine, AbbVie Bioresearch Center, Worcester, MA 01605, United States.

出版信息

J Pharm Sci. 2024 Sep;113(9):2967-2973. doi: 10.1016/j.xphs.2024.05.034. Epub 2024 Jun 12.

Abstract

The use of recombinant adeno-associated virus (AAV) vectors is a popular choice for in vivo gene therapy, with hundreds of ongoing clinical trials targeting various genetic diseases. However, due to limited material availability and the complexity of AAV structure, there is a critical lack of comprehensive studies on AAV degradation pathways. In this study, we intended to elucidate the degradation pathways for a model AAV9 with GFP as the transgene under relevant stressed conditions. We assessed a diverse set of critical quality attributes and examined the overall impact of various stresses on transgene expression. This assessment revealed various degradation mechanisms of AAV9 and demonstrated the potential risk of a base formulation in causing AAV9 instability and potency loss under thermal stress at 25 and 40 °C while maintaining stability under freeze-thaw stress, interfacial stress due to membrane filtration, and short-term storage of up to 4 weeks at 5 °C.

摘要

腺相关病毒(AAV)载体的使用是体内基因治疗的热门选择,目前有数百项针对各种遗传疾病的临床试验正在进行。然而,由于有限的材料可用性和 AAV 结构的复杂性,对 AAV 降解途径的综合研究还很缺乏。在这项研究中,我们旨在阐明携带 GFP 作为转基因的模型 AAV9 在相关应激条件下的降解途径。我们评估了一系列关键质量属性,并研究了各种应激对转基因表达的整体影响。这项评估揭示了 AAV9 的多种降解机制,并表明基础配方在 25 和 40°C 的热应激下可能导致 AAV9 不稳定和效力丧失,而在冻融应激、膜过滤引起的界面应激以及在 5°C 下长达 4 周的短期储存中保持稳定的潜在风险。

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