Process & Product Development, Vir Biotechnology Inc, San Francisco, CA, USA.
MAbs. 2024 Jan-Dec;16(1):2373330. doi: 10.1080/19420862.2024.2373330. Epub 2024 Jul 1.
Therapeutic monoclonal antibody (mAb) development and the processes for manufacturing drug substance have evolved since the first approval of the mAb in 1986. As the past is often the prologue to the future, the history of these technologies has been classified here into three eras, leading to speculation about what the next era may hold with regard to development and manufacturing strategies, as well as the potential impacts to patients. The substantial increase in production culture titers and bioreactor production volumes and the availability of large-scale contract manufacturing facilities could translate into improved global access for these therapies and an expansion of indications for therapeutic antibodies.
自 1986 年首个治疗性单克隆抗体 (mAb) 获得批准以来,治疗性 mAb 的开发和药物物质制造工艺已经发展。过去常常是未来的序幕,因此这里将这些技术的历史分为三个时代,以期推测未来在开发和制造策略方面可能会有哪些发展,以及对患者的潜在影响。生产培养滴度和生物反应器生产体积的大幅增加,以及大型合同制造设施的可用性,可能会使这些疗法在全球范围内更容易获得,并扩大治疗性抗体的适应证。