Center for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agency, 177 Hyeoksin 8-ro, Gimcheon-City, Gyeongsangbuk-do, Republic of Korea.
Center for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agency, 177 Hyeoksin 8-ro, Gimcheon-City, Gyeongsangbuk-do, Republic of Korea.
Antiviral Res. 2022 Sep;205:105384. doi: 10.1016/j.antiviral.2022.105384. Epub 2022 Jul 19.
Foot-and-mouth disease (FMD) is an acute contagious disease of cloven-hoofed animals such as cows, pigs, sheep, and deer. The current emergency FMD vaccines, to induce early protection, have limited use, as their protective effect in pigs does not begin until 7 days after vaccination. Therefore, the use of antiviral agents would be required for reducing the spread of foot-and-mouth disease virus (FMDV) during outbreaks. Vesatolimod (GS-9620), a toll-like receptor 7 agonist, is an antiviral agent against various human disease-causing viruses. However, its antiviral effect against FMDV has not been reported yet. The aim of this study was to investigate the antiviral effects of GS-9620 against FMDV both in vitro and in vivo. The inhibitory effect of GS-9620 on FMDV in swine cells involved the induction of porcine interferon (IFN)-α and upregulation of interferon-simulated genes. Protective effect in mice injected with GS-9620 against FMDV was maintained for 5 days after injection, and cytokines such as IFN-γ, interleukin (IL)-12, IL-6, and IFN-γ inducible protein-10 could be detected following the treatment with GS-9620. Furthermore, the combination of GS-9620 with an FMD-inactivated vaccine was found to be highly effective for early protection in mice. Overall, we suggest GS-9620 as a novel and effective antiviral agent for controlling FMDV infection.
口蹄疫(FMD)是一种急性传染病,主要发生在牛、猪、羊、鹿等偶蹄类动物中。目前的紧急口蹄疫疫苗主要用于诱导早期保护,但其在猪中的保护作用要在接种后 7 天才能开始,因此在暴发期间需要使用抗病毒药物来减少口蹄疫病毒(FMDV)的传播。Vesatolimod(GS-9620)是一种 Toll 样受体 7 激动剂,是一种针对多种人类致病病毒的抗病毒药物。然而,其对口蹄疫病毒的抗病毒作用尚未有报道。本研究旨在探讨 GS-9620 对 FMDV 的体内外抗病毒作用。GS-9620 对猪细胞中 FMDV 的抑制作用涉及诱导猪干扰素(IFN)-α和干扰素刺激基因的上调。GS-9620 对感染 FMDV 的小鼠的保护作用可维持 5 天,并且在治疗后可检测到 IFN-γ、白细胞介素(IL)-12、IL-6 和 IFN-γ 诱导蛋白-10 等细胞因子。此外,GS-9620 与 FMD 灭活疫苗联合使用在小鼠中具有高度的早期保护作用。总之,我们认为 GS-9620 是一种控制 FMDV 感染的新型有效抗病毒药物。