Castro Leonor S, Lobo Guilherme S, Pereira Patrícia, Freire Mara G, Neves Márcia C, Pedro Augusto Q
CICECO-Aveiro Institute of Materials, Chemistry Department, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
Centre for Mechanical Engineering, Materials and Processes, Department of Chemical Engineering, University of Coimbra, Rua Sílvio Lima-Polo II, 3030-790 Coimbra, Portugal.
Vaccines (Basel). 2021 Apr 1;9(4):328. doi: 10.3390/vaccines9040328.
The advent of biopharmaceuticals in modern medicine brought enormous benefits to the treatment of numerous human diseases and improved the well-being of many people worldwide. First introduced in the market in the early 1980s, the number of approved biopharmaceutical products has been steadily increasing, with therapeutic proteins, antibodies, and their derivatives accounting for most of the generated revenues. The success of pharmaceutical biotechnology is closely linked with remarkable developments in DNA recombinant technology, which has enabled the production of proteins with high specificity. Among promising biopharmaceuticals are interferons, first described by Isaacs and Lindenmann in 1957 and approved for clinical use in humans nearly thirty years later. Interferons are secreted autocrine and paracrine proteins, which by regulating several biochemical pathways have a spectrum of clinical effectiveness against viral infections, malignant diseases, and multiple sclerosis. Given their relevance and sustained market share, this review provides an overview on the evolution of interferon manufacture, comprising their production, purification, and formulation stages. Remarkable developments achieved in the last decades are herein discussed in three main sections: (i) an upstream stage, including genetically engineered genes, vectors, and hosts, and optimization of culture conditions (culture media, induction temperature, type and concentration of inducer, induction regimens, and scale); (ii) a downstream stage, focusing on single- and multiple-step chromatography, and emerging alternatives (e.g., aqueous two-phase systems); and (iii) formulation and delivery, providing an overview of improved bioactivities and extended half-lives and targeted delivery to the site of action. This review ends with an outlook and foreseeable prospects for underdeveloped aspects of biopharma research involving human interferons.
生物制药在现代医学中的出现给众多人类疾病的治疗带来了巨大益处,并改善了全球许多人的健康状况。20世纪80年代初首次投放市场以来,获批的生物制药产品数量一直在稳步增加,治疗性蛋白质、抗体及其衍生物占了大部分创收。制药生物技术的成功与DNA重组技术的显著发展密切相关,DNA重组技术使高特异性蛋白质的生产成为可能。有前景的生物制药产品包括干扰素,它于1957年由艾萨克斯和林登曼首次描述,近三十年后被批准用于人类临床。干扰素是自分泌和旁分泌蛋白,通过调节多种生化途径,对病毒感染、恶性疾病和多发性硬化症具有一系列临床疗效。鉴于其相关性和持续的市场份额,本综述概述了干扰素生产的演变,包括其生产、纯化和制剂阶段。本文在三个主要部分讨论了过去几十年取得的显著进展:(i)上游阶段,包括基因工程基因、载体和宿主,以及培养条件(培养基、诱导温度、诱导剂类型和浓度、诱导方案和规模)的优化;(ii)下游阶段,重点是单步和多步色谱法以及新兴替代方法(如水相两相系统);(iii)制剂和递送,概述了改善的生物活性、延长的半衰期以及靶向作用部位的递送。本综述最后展望了涉及人类干扰素的生物制药研究未开发方面的前景和可预见的前景。