Laboratory of Anti-oxidant Immunology and Vitamin C, Department of Anatomy, Seoul National University College of Medicine, Seoul 110-799, Korea.
Immune Netw. 2013 Apr;13(2):70-4. doi: 10.4110/in.2013.13.2.70. Epub 2013 Apr 30.
L-ascorbic acid (vitamin C) is one of the well-known anti-viral agents, especially to influenza virus. Since the in vivo anti-viral effect is still controversial, we investigated whether vitamin C could regulate influenza virus infection in vivo by using Gulo (-/-) mice, which cannot synthesize vitamin C like humans. First, we found that vitamin C-insufficient Gulo (-/-) mice expired within 1 week after intranasal inoculation of influenza virus (H3N2/Hongkong). Viral titers in the lung of vitamin C-insufficient Gulo (-/-) mice were definitely increased but production of anti-viral cytokine, interferon (IFN)-α/β, was decreased. On the contrary, the infiltration of inflammatory cells into the lung and production of pro-inflammatory cytokines, tumor necrosis factor (TNF)-α and interleukin (IL)-α/β, were increased in the lung. Taken together, vitamin C shows in vivo anti-viral immune responses at the early time of infection, especially against influenza virus, through increased production of IFN-α/β.
L-抗坏血酸(维生素 C)是一种众所周知的抗病毒药物,尤其对流感病毒有效。由于其体内抗病毒作用仍存在争议,我们通过使用类似于人类无法合成维生素 C 的 Gulo(-/-)小鼠来研究维生素 C 是否可以调节体内流感病毒感染。首先,我们发现,在鼻腔接种流感病毒(H3N2/香港)后,维生素 C 不足的 Gulo(-/-)小鼠在 1 周内死亡。维生素 C 不足的 Gulo(-/-)小鼠肺部的病毒滴度明显增加,但抗病毒细胞因子干扰素(IFN)-α/β的产生减少。相反,肺部炎症细胞的浸润和促炎细胞因子肿瘤坏死因子(TNF)-α和白细胞介素(IL)-α/β的产生增加。总之,维生素 C 通过增加 IFN-α/β的产生,在感染的早期表现出体内抗病毒免疫反应,特别是针对流感病毒。