Gradutae School of Medicine and Pharmaceutical Sciences for Research, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan,
Arch Virol. 2014 Mar;159(3):425-35. doi: 10.1007/s00705-013-1829-x. Epub 2013 Sep 18.
Herpes simplex virus types 1 (HSV-1) and 2 (HSV-2) cause genital herpes, which can enhance the acquisition of human immunodeficiency virus. The development of anti-HSV agents with novel mechanisms of action is urgently required in the topical therapy of genital herpes. In this study, the in vitro and in vivo anti-HSV effects of Epomin SP-012(®), a highly cationic polyethylenimine, were evaluated. When the in vitro antiviral effects of SP-012 were assessed, this compound showed potent activity against HSV-1 and HSV-2. It inhibited the attachment of HSV-2 to host cells and cell-to-cell spread of infection in a concentration-dependent manner and exerted a virucidal effect. No SP-012-resistant HSV-2 was found when the virus was successively passaged in the presence of SP-012. In a mouse genital herpes model, topically administered SP-012 inhibited the progression of the disease caused by HSV infection. These data illustrate that SP-012 may be a novel class of HSV inhibitor that would be acceptable for long-term topical application.
单纯疱疹病毒 1 型(HSV-1)和 2 型(HSV-2)引起生殖器疱疹,这可能会增加人类免疫缺陷病毒的感染风险。因此,迫切需要开发具有新型作用机制的抗 HSV 药物,用于生殖器疱疹的局部治疗。在这项研究中,评估了高度阳离子聚乙烯亚胺 Epomin SP-012(®) 在体外和体内的抗 HSV 作用。当评估 SP-012 的体外抗病毒作用时,发现该化合物对 HSV-1 和 HSV-2 具有很强的活性。它以浓度依赖的方式抑制 HSV-2 与宿主细胞的附着和细胞间感染的传播,并发挥溶病毒作用。当在 SP-012 存在的情况下连续传代病毒时,没有发现对 SP-012 有抗性的 HSV-2。在小鼠生殖器疱疹模型中,局部给予 SP-012 可抑制由 HSV 感染引起的疾病进展。这些数据表明,SP-012 可能是一种新型的 HSV 抑制剂,可接受长期局部应用。