Lagassé H A Daniel, Alexaki Aikaterini, Simhadri Vijaya L, Katagiri Nobuko H, Jankowski Wojciech, Sauna Zuben E, Kimchi-Sarfaty Chava
Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD, USA.
F1000Res. 2017 Feb 7;6:113. doi: 10.12688/f1000research.9970.1. eCollection 2017.
Therapeutic protein drugs are an important class of medicines serving patients most in need of novel therapies. Recently approved recombinant protein therapeutics have been developed to treat a wide variety of clinical indications, including cancers, autoimmunity/inflammation, exposure to infectious agents, and genetic disorders. The latest advances in protein-engineering technologies have allowed drug developers and manufacturers to fine-tune and exploit desirable functional characteristics of proteins of interest while maintaining (and in some cases enhancing) product safety or efficacy or both. In this review, we highlight the emerging trends and approaches in protein drug development by using examples of therapeutic proteins approved by the U.S. Food and Drug Administration over the previous five years (2011-2016, namely January 1, 2011, through August 31, 2016).
治疗性蛋白质药物是一类重要的药物,为最需要新型疗法的患者提供服务。最近获批的重组蛋白质疗法已被开发用于治疗多种临床病症,包括癌症、自身免疫/炎症、接触传染原以及遗传性疾病。蛋白质工程技术的最新进展使药物开发者和制造商能够在保持(在某些情况下还能提高)产品安全性或疗效或两者的同时,对感兴趣蛋白质的理想功能特性进行微调并加以利用。在本综述中,我们通过列举美国食品药品监督管理局在过去五年(2011年至2016年,即2011年1月1日至2016年8月31日)批准的治疗性蛋白质实例,重点介绍蛋白质药物开发中的新兴趋势和方法。