Fuchizaki Uichiro, Kaneko Shuichi, Nakamoto Yasunari, Sugiyama Yoshihiro, Imagawa Kenichi, Kikuchi Mikio, Kobayashi Kenichi
Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Ishikawa, Japan.
J Med Virol. 2003 Feb;69(2):188-94. doi: 10.1002/jmv.10286.
Although interferon (IFN)-alpha and IFN-gamma have been reported to exhibit a synergistic antiviral effect through the different signaling pathways in vitro, their therapeutic efficacy is not well defined in vivo. The current study was carried out to investigate the combined antiviral effect in a model of mouse hepatitis virus Type 2 (MHV-2) infection, in which fulminant hepatitis is developed. MHV-2 was injected intraperitoneally into 4-week-old ICR mice, IFN or the vehicle was administered intramuscularly for 5 days, and the antiviral effect was evaluated based on survival periods, liver histology, serum alanine transaminase (ALT) levels, and MHV-2 virus titers in the liver tissues. The animals in the group treated with a combination of IFN-alpha and IFN-gamma survived for longer periods than the groups treated with IFN-alpha alone and IFN-gamma alone (IFN-alpha 10(3) (IU/mouse)/-gamma 10(3) vs. IFN-alpha 10(3), P < 0.005; IFN-alpha 10(3)/-gamma 10(3) vs. IFN-gamma 10(3), P < 0.001). This is consistent with the lower levels of hepatocellular necrosis and serum ALT and the decreased titers of MHV-2 virus in the liver tissues (48 hr, P < 0.001; 72 hr, P < 0.001). These findings indicate that a combination of IFN-alpha and IFN-gamma exhibits a synergistic antiviral effect on MHV-2 infection. The biology of MHV-2 is quite different from that of human hepatitis viruses; however, these results suggest the beneficial combined therapy of IFN-alpha and IFN-gamma for the treatment of human viral hepatitis.
虽然据报道,α干扰素(IFN-α)和γ干扰素(IFN-γ)在体外可通过不同的信号通路发挥协同抗病毒作用,但其体内治疗效果尚不明确。本研究旨在探讨在2型小鼠肝炎病毒(MHV-2)感染模型中的联合抗病毒作用,该模型会引发暴发性肝炎。将MHV-2腹腔注射到4周龄的ICR小鼠体内,肌肉注射IFN或赋形剂,持续5天,并根据生存期、肝脏组织学、血清丙氨酸转氨酶(ALT)水平以及肝脏组织中的MHV-2病毒滴度评估抗病毒效果。联合使用IFN-α和IFN-γ治疗的组动物生存期比单独使用IFN-α和单独使用IFN-γ治疗的组更长(IFN-α 10³(IU/小鼠)/IFN-γ 10³ 对比 IFN-α 10³,P < 0.005;IFN-α 10³/IFN-γ 10³ 对比 IFN-γ 10³,P < 0.001)。这与肝细胞坏死程度降低、血清ALT水平降低以及肝脏组织中MHV-2病毒滴度降低一致(48小时,P < 0.001;72小时,P < 0.001)。这些发现表明,IFN-α和IFN-γ联合使用对MHV-2感染具有协同抗病毒作用。MHV-2的生物学特性与人类肝炎病毒有很大不同;然而,这些结果提示IFN-α和IFN-γ联合治疗对人类病毒性肝炎可能有益。