Molecular pharming in plants and plant cell cultures: a great future ahead?

A. Ritala, S. Häkkinen, S. Schillberg
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引用次数: 8

Abstract

Plant biotechnology may not be a familiar concept to the general public, but it is a rapidly developing field of research that involves the use of plants, plant tissues and plant cell cultures to make or modify products and processes. The versatility of plants and plant cells can be harnessed to produce diverse products, including valuable proteins. This is often described as ‘molecular farming’ and it requires the introduction of foreign DNA into plants or plant cells, turning them into factories for the production of specific recombinant protein products. The term ‘molecular pharming’ is often used instead to highlight the production of protein-based biopharmaceuticals, which contributes to the sustainable production of drugs that promote human and animal wellbeing. Both terms also apply to the production of valuable secondary metabolites such as the anticancer drugs paclitaxel, vincristine and vinblastine, but we will focus on recombinant proteins and their use as biopharmaceuticals in this article. The biopharmaceutical markets have expanded rapidly over the last 20 years, and are projected to more than double in volume over the next decade from US$200 billion in 2013 to at least US$500 billion in 2020. The two major biopharmaceutical production systems are microbes (mainly Escherichia coli and yeast) and mammalian cells such as the Chinese hamster ovary platform. In both cases, productivity has increased substantially over the last decade due to process optimization, platform standardization and genetic improvements. Both the US FDA and European Medicines Agency are familiar with these systems, and standard protocols can be followed to ensure the approval of new products. However, equivalent protocols are only just emerging for plant-based production systems, and only one plant-derived biopharmaceutical protein is currently on the market. With their established production infrastructure and regulatory framework, microbial and mammalian production systems have raced far ahead of their plant-based counterparts. No company will change their production host without a clear economic benefit, nor will they consider plants and plant cells for new products if there is no advantage over their incumbent technology. Furthermore, new companies will not base their manufacturing on a second-best option. Therefore, plant-based systems must begin to compete head-to-head with the established systems and, on a technological basis, we can already identify the areas where plantbased systems have the advantage, namely in terms of speed, improved product quality and scalability. The international success story of molecular pharming began in 2006 with the US Department of Agriculture approval of a poultry vaccine against Newcastle disease developed by Dow AgroSciences (IN, USA) [1,2]. The vaccine was manufactured in transgenic tobacco cell suspension cultures and was a benchmark for the regulatory acceptance of plants as a manufacturing platform, Molecular pharming in plants and plant cell cultures: a great future ahead?
植物分子药剂学和植物细胞培养:一个伟大的未来?
植物生物技术对一般公众来说可能不是一个熟悉的概念,但它是一个迅速发展的研究领域,涉及利用植物、植物组织和植物细胞培养来制造或修改产品和工艺。植物和植物细胞的多功能性可以用来生产各种产品,包括有价值的蛋白质。这通常被称为“分子农业”,它需要将外源DNA引入植物或植物细胞,将它们变成生产特定重组蛋白产品的工厂。“分子制药”一词通常用来强调以蛋白质为基础的生物制药的生产,这有助于促进人类和动物健康的药物的可持续生产。这两个术语也适用于生产有价值的次级代谢物,如抗癌药物紫杉醇、长春新碱和长春花碱,但我们将在本文中重点讨论重组蛋白及其作为生物制药的用途。生物制药市场在过去20年中迅速扩大,预计未来10年的规模将增加一倍以上,从2013年的2000亿美元增至2020年的至少5000亿美元。两个主要的生物制药生产系统是微生物(主要是大肠杆菌和酵母)和哺乳动物细胞,如中国仓鼠卵巢平台。在这两种情况下,由于流程优化、平台标准化和遗传改进,生产力在过去十年中大幅提高。美国食品药品监督管理局和欧洲药品管理局都熟悉这些系统,并且可以遵循标准协议来确保新产品的批准。然而,基于植物的生产系统的等效方案才刚刚出现,目前市场上只有一种植物来源的生物制药蛋白。凭借其已建立的生产基础设施和监管框架,微生物和哺乳动物生产系统远远领先于植物生产系统。如果没有明显的经济效益,没有公司会改变他们的生产主机,如果没有现有技术的优势,他们也不会考虑为新产品生产工厂和植物细胞。此外,新公司不会把生产建立在次优选择上。因此,基于植物的系统必须开始与已建立的系统进行正面竞争,并且在技术基础上,我们已经可以确定基于植物的系统具有优势的领域,即在速度,改进的产品质量和可扩展性方面。分子制药的国际成功故事始于2006年,当时美国农业部批准了陶氏农业科学公司(in, USA)开发的一种抗新城疫的家禽疫苗[1,2]。该疫苗是在转基因烟草细胞悬浮培养物中生产的,是监管机构接受植物作为生产平台的基准。植物分子制药和植物细胞培养物:未来美好?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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