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腺相关病毒灌注增强表达:一种具有商业可扩展性、高滴度、高质量的生产细胞系工艺。

Adeno-associated virus perfusion enhanced expression: A commercially scalable, high titer, high quality producer cell line process.

作者信息

Xue Wei, Fulco Cameron, Sha Sha, Alden Nick, Panteli Jan, Hossler Patrick, Warren James

机构信息

Ultragenyx Pharmaceutical Inc., Global CMC Development, 19 Presidential Way, Woburn, MA 01801, USA.

出版信息

Mol Ther Methods Clin Dev. 2024 May 14;32(2):101266. doi: 10.1016/j.omtm.2024.101266. eCollection 2024 Jun 13.

Abstract

With safety and efficacy demonstrated over hundreds of clinical trials in the last 30 years, along with at least six recent global marketing authorizations achieved since 2017, recombinant adeno-associated viruses (rAAVs) have been established as the leading therapeutic gene transfer vector for rare, monogenic diseases. Significant advances in manufacturing technology have been made in the last few decades to address challenges with GMP production of rAAV products, although yield, cost, scalability, and quality remain a challenge. With transient transfection processes established as a manufacturing platform for multiple commercial AAV products, there remains significant yield, cost, robustness, and scalability constraints that need to be resolved to enable a reliable supply of rAAV products for global patient access. The development of stable producer cell lines for rAAV products has enabled scalability and, in some cases, improvements in productivity. Herein we describe a novel AAV perfusion-enhanced expression (APEX) process, resulting in higher maximum cell densities in the production bioreactor with a 3- to 6-fold increase in volumetric productivity. This process has been successfully demonstrated across multiple serotypes in large scale cell culture with titers approaching 1 × 10 GC/mL. The APEX production platform marks a significant leap forward in the efficient and effective manufacturing of rAAV vector products.

摘要

在过去30年的数百项临床试验中,重组腺相关病毒(rAAV)的安全性和有效性得到了证实,自2017年以来至少获得了六项全球上市许可,已成为治疗罕见单基因疾病的主要治疗性基因转移载体。尽管产量、成本、可扩展性和质量仍然是挑战,但在过去几十年里,制造技术取得了重大进展,以应对rAAV产品的GMP生产挑战。随着瞬时转染工艺成为多种商业AAV产品的制造平台,仍存在显著的产量、成本、稳健性和可扩展性限制,需要加以解决,以便为全球患者提供可靠的rAAV产品供应。rAAV产品稳定生产细胞系的开发实现了可扩展性,在某些情况下还提高了生产力。在此,我们描述了一种新型的AAV灌注增强表达(APEX)工艺,该工艺可使生产生物反应器中的最大细胞密度更高,体积生产力提高3至6倍。该工艺已在大规模细胞培养中的多种血清型中成功得到验证,滴度接近1×10 GC/mL。APEX生产平台标志着rAAV载体产品高效生产方面的重大飞跃。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/11166877/06c910d71750/fx1.jpg

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