Malinoski F J, Hasty S E, Ussery M A, Dalrymple J M
Virology Division, U.S. Army Medical Research Institute of Infectious Diseases, Ft. Detrick, Frederick, MD 21701-5011.
Antiviral Res. 1990 Mar;13(3):139-49. doi: 10.1016/0166-3542(90)90029-7.
The prophylactic efficacy of the broad-spectrum antiviral nucleoside analog ribavirin against flavivirus infection in non-human primates was investigated in a blinded, placebo-controlled study of rhesus monkeys infected with dengue virus. Both placebo- and ribavirin-treated monkeys developed viremia, as measured by direct plaque assay on Aedes albopictus C6/36 cells. Peak viremia occurred between days 3 and 9 after infection. No significant differences in time of onset, duration, or level of viremia were observed between placebo- and ribavirin-treated monkeys. Ribavirin induced predictable and reversible anemia and thrombocytosis. Serum ribavirin reached maximum levels of 30 microM by day 4, which approximates the in vitro minimum inhibitory concentration for dengue virus. Ribavirin appeared ineffective as a prophylactic drug for dengue type 1 viral infection, as evaluated by the magnitude of viremia in this monkey model.
在一项针对感染登革病毒的恒河猴的双盲、安慰剂对照研究中,研究了广谱抗病毒核苷类似物利巴韦林对非人灵长类动物黄病毒感染的预防效果。通过对白纹伊蚊C6/36细胞进行直接空斑试验测定,接受安慰剂和利巴韦林治疗的猴子均出现病毒血症。病毒血症高峰出现在感染后第3至9天。在接受安慰剂和利巴韦林治疗的猴子之间,未观察到病毒血症的发病时间、持续时间或水平有显著差异。利巴韦林会引起可预测且可逆的贫血和血小板增多症。血清利巴韦林在第4天达到30微摩尔的最高水平,这接近登革病毒的体外最低抑菌浓度。根据该猴子模型中病毒血症的程度评估,利巴韦林作为预防1型登革病毒感染的药物似乎无效。