Hsieh I-Ni, Hartshorn Kevan L
Department of Medicine, Boston University School of Medicine, Boston, MA 02118, USA.
Pharmaceuticals (Basel). 2016 Sep 6;9(3):53. doi: 10.3390/ph9030053.
Influenza A virus (IAV) remains a major threat that can cause severe morbidity and mortality due to rapid genomic variation. Resistance of IAVs to current anti-IAV drugs has been emerging, and antimicrobial peptides (AMPs) have been considered to be potential candidates for novel treatment against IAV infection. AMPs are endogenous proteins playing important roles in host defense through direct antimicrobial and antiviral activities and through immunomodulatory effects. In this review, we will discuss the anti-IAV and immunomodulatory effects of classical AMPs (defensins and cathelicidins), and proteins more recently discovered to have AMP-like activity (histones and Alzheimer's associated β-amyloid). We will discuss the interactions between AMPs and other host defense proteins. Major emphasis will be placed on novel synthetic AMPs derived from modification of natural proteins, and on potential methods of increasing expression of endogenous AMPs, since these approaches may lead to novel antiviral therapeutics.
甲型流感病毒(IAV)仍然是一个重大威胁,因其基因组快速变异,可导致严重发病和死亡。IAV对当前抗IAV药物的耐药性不断出现,抗菌肽(AMPs)被认为是对抗IAV感染的新型治疗潜在候选物。AMPs是内源性蛋白质,通过直接抗菌和抗病毒活性以及免疫调节作用在宿主防御中发挥重要作用。在本综述中,我们将讨论经典AMPs(防御素和cathelicidins)以及最近发现具有AMPs样活性的蛋白质(组蛋白和阿尔茨海默病相关β-淀粉样蛋白)的抗IAV和免疫调节作用。我们将讨论AMPs与其他宿主防御蛋白之间的相互作用。主要重点将放在源自天然蛋白质修饰的新型合成AMPs以及增加内源性AMPs表达的潜在方法上,因为这些方法可能会带来新型抗病毒疗法。