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Development of anti-infectives using phage display: biological agents against bacteria, viruses, and parasites

机译:使用噬菌体展示技术开发抗感染药:针对细菌,病毒和寄生虫的生物制剂

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摘要

The vast majority of anti-infective therapeutics on the market or in development are small molecules; however, there is now a nascent pipeline of biological agents in development. Until recently, phage display technologies were used mainly to produce monoclonal antibodies (MAbs) targeted against cancer or inflammatory disease targets. Patent disputes impeded broad use of these methods and contributed to the dearth of candidates in the clinic during the 1990s. Today, however, phage display is recognized as a powerful tool for selecting novel peptides and antibodies that can bind to a wide range of antigens, ranging from whole cells to proteins and lipid targets. In this review, we highlight research that exploits phage display technology as a means of discovering novel therapeutics against infectious diseases, with a focus on antimicrobial peptides and antibodies in clinical or preclinical development. We discuss the different strategies and methods used to derive, select, and develop anti-infectives from phage display libraries and then highlight case studies of drug candidates in the process of development and commercialization. Advances in screening, manufacturing, and humanization technologies now mean that phage display can make a significant contribution in the fight against clinically important pathogens.
机译:市场上或开发中的绝大多数抗感染治疗药物都是小分子。但是,现在有新生的生物制剂正在开发中。直到最近,噬菌体展示技术主要用于产生针对癌症或炎性疾病靶标的单克隆抗体(MAb)。专利纠纷阻碍了这些方法的广泛使用,并导致1990年代诊所候选人的匮乏。然而,如今,噬菌体展示已被认为是一种选择新型肽和抗体的有力工具,这些肽和抗体可以与多种抗原结合,从整个细胞到蛋白质和脂质靶标。在这篇综述中,我们重点介绍利用噬菌体展示技术作为发现针对传染病的新型疗法的手段的研究,重点是临床或临床前开发中的抗菌肽和抗体。我们讨论了用于从噬菌体展示库衍生,选择和开发抗感染剂的不同策略和方法,然后重点介绍了在开发和商业化过程中候选药物的案例研究。现在,筛选,生产和人源化技术的进步意味着噬菌体展示可以在对抗临床上重要的病原体方面做出重要贡献。

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