Schul Wouter, Liu Wei, Xu Hao-Ying, Flamand Marie, Vasudevan Subhash G
Novartis Institute for Tropical Diseases, Chromos, Singapore.
J Infect Dis. 2007 Mar 1;195(5):665-74. doi: 10.1086/511310. Epub 2007 Jan 23.
Dengue fever is an emerging arboviral disease for which no vaccine or antiviral treatment exists and that causes thousands of fatalities each year. To develop an in vivo test system for antidengue drugs, AG129 mice, which are deficient for the interferon- alpha / beta and - gamma receptors, were injected with unadapted dengue virus, resulting in a dose-dependent transient viremia lasting several days and peaking on day 3 after infection. Additionally, nonstructural protein 1, increased levels of proinflammatory cytokines, and neutralizing IgM and IgG antibodies were found, and mice had splenomegaly. Oral administration of the antiviral compounds 7-deaza-2'-C-methyl-adenosine, N-nonyl-deoxynojirimycin, or 6-O-butanoyl castanospermine significantly reduced viremia in a dose-dependent manner, even after delayed treatment, leading to a reduction of splenomegaly and proinflammatory cytokine levels. The results validate this dengue viremia mouse model as a suitable system for testing antidengue drugs and indicate that antiviral treatment during the acute phase of dengue fever can reduce the severity of the disease.
登革热是一种新出现的虫媒病毒疾病,目前尚无疫苗或抗病毒治疗方法,每年导致数千人死亡。为了开发一种用于抗登革热药物的体内测试系统,给缺乏α/β干扰素和γ干扰素受体的AG129小鼠注射未适应的登革病毒,导致出现持续数天的剂量依赖性短暂病毒血症,并在感染后第3天达到峰值。此外,还发现了非结构蛋白1、促炎细胞因子水平升高以及中和性IgM和IgG抗体,并且小鼠出现脾肿大。口服抗病毒化合物7-脱氮-2'-C-甲基腺苷、N-壬基-脱氧野尻霉素或6-O-丁酰基栗精胺即使在延迟治疗后也能以剂量依赖性方式显著降低病毒血症,从而减轻脾肿大和促炎细胞因子水平。这些结果证实了这种登革病毒血症小鼠模型是测试抗登革热药物的合适系统,并表明在登革热急性期进行抗病毒治疗可以减轻疾病的严重程度。