加速大规模、全长、类人糖基化生物防御抗体的生产。

Christopher M. Warner, M. Croughan
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引用次数: 5

摘要

从DNA序列确认到生产有意义的临床数量的新疗法,目前许多糖基化蛋白的制造系统需要几个月的开发。因此,在发生大规模伤亡流行病时,现有系统将无法提供足够和及时的紧急医疗应对措施。由于许多新的生物威胁的性质不太可能事先知道,因此不可能总是先发制人地制造和储存对抗措施。为所有生物灾难做好准备需要一个彻底的解决办法,以取代目前缓慢扩大和制造某些挽救生命的医疗对策的做法。目前的临床和商业糖基化蛋白的制造方法使用稳定的细胞系进行蛋白表达,其中目标蛋白的基因编码稳定地整合到宿主细胞基因组中。生成、识别、存储、测试和扩展合适的稳定克隆通常需要几个月的时间。由于这种开发时间与应急生产不兼容,因此需要一种快速生产医疗对抗抗体的替代方法。其中一个潜在的技术是瞬时基因表达。瞬时基因表达是生产研究级抗体的常用方法。它通常用于在DNA序列确认后的两到三周内生成毫克到克的物质。过去,瞬态系统曾被考虑用于大量抗体的紧急生产,但由于低效价、DNA成本高、监管环境不确定以及缺乏足够的、可用的制造能力而被忽视。然而,最近的事态发展大大加强了这种办法的可行性。本文将探讨这些发展,并研究利用瞬时基因表达快速生产基于抗体的医疗对策。
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Accelerated manufacturing of large-scale, full-length, human-like glycosylated antibodies for bio-defense.
From the point of DNA sequence confirmation until production of meaningful clinical quantities of novel therapeutics, current manufacturing systems for many glycosylated proteins require several months of development. Consequently, in the event of mass-casualty epidemics, current systems will fail to provide sufficient and timely quantities of emergency medical counter measures. As the identity of many new biological threats are unlikely to be known in advance, pre-emptive manufacturing and stockpiling of countermeasures cannot always be performed. Preparedness for all biological catastrophes requires a radical solution to replace the current slow scale-up and manufacture of certain lifesaving medical countermeasures. Current clinical and commercial manufacturing methods for glycosylated proteins use stable cell lines for protein expression, wherein the gene coding for the protein of interest is stably integrated into the host cell genome. The generation, identification, banking, testing, and scale-up of suitable stable clones generally takes many months. Because this development time is not compatible with emergency manufacturing, an alternative method for rapid production of medical counter measure antibodies is needed. One such potential technique is transient gene expression. Transient gene expression is a common approach for production of research-grade antibodies. It is frequently used to generate milligram to gram quantities of material within two to three weeks of DNA sequence confirmation. In the past, transient systems have been considered for emergency production of large quantities of antibodies, but dismissed due to low titers, high cost of DNA, uncertain regulatory environment, and the lack of sufficient, available manufacturing capacity. Recent developments, however, have substantially enhanced the viability of such an approach. This article will explore these developments and investigate the use of transient gene expression for rapid production of antibody-based medical countermeasures.
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