MRC Centre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, Scotland, UK.
BioDrugs. 2013 Oct;27(5):479-93. doi: 10.1007/s40259-013-0039-0.
There is a pressing need to develop new antiviral treatments; of the 60 drugs currently available, half are aimed at HIV-1 and the remainder target only a further six viruses. This demand has led to the emergence of possible peptide therapies, with 15 currently in clinical trials. Advancements in understanding the antiviral potential of naturally occurring host defence peptides highlights the potential of a whole new class of molecules to be considered as antiviral therapeutics. Cationic host defence peptides, such as defensins and cathelicidins, are important components of innate immunity with antimicrobial and immunomodulatory capabilities. In recent years they have also been shown to be natural, broad-spectrum antivirals against both enveloped and non-enveloped viruses, including HIV-1, influenza virus, respiratory syncytial virus and herpes simplex virus. Here we review the antiviral properties of several families of these host peptides and their potential to inform the design of novel therapeutics.
目前迫切需要开发新的抗病毒治疗方法;在目前可用的 60 种药物中,有一半针对 HIV-1,其余仅针对另外六种病毒。这种需求导致了可能的肽疗法的出现,目前有 15 种处于临床试验阶段。对天然宿主防御肽的抗病毒潜力的深入了解突显了一类全新的分子作为抗病毒治疗药物的潜力。阳离子宿主防御肽,如防御素和 cathelicidins,是先天免疫的重要组成部分,具有抗菌和免疫调节功能。近年来,它们还被证明是天然的广谱抗病毒药物,可对抗包膜和非包膜病毒,包括 HIV-1、流感病毒、呼吸道合胞病毒和单纯疱疹病毒。在这里,我们回顾了这些宿主肽的几个家族的抗病毒特性及其为新型治疗药物设计提供信息的潜力。