Schinazi R F, Peters J, Williams C C, Chance D, Nahmias A J
Antimicrob Agents Chemother. 1982 Sep;22(3):499-507. doi: 10.1128/AAC.22.3.499.
The combination of various concentrations of acyclovir and vidarabine or its 5'-monophosphate usually produced an additive interaction with various strains of herpes simplex virus types 1 and 2 in Vero cells. Similarly, certain combinations of these drugs were more effective than the individual drugs in decreasing the mortality and increasing the mean day of death of mice inoculated intracerebrally with herpes simplex virus type 2. Neither antagonism nor interference was noted for any of the in vitro or in vivo combinations. The increased antiviral activity was determined not to be secondary to toxic effects of the drugs. Although viruses resistant to either vidarabine or acyclovir developed readily in cell culture, no evidence of cross-resistance was obtained. Furthermore, in the presence of the two drugs, mutants resistant to vidarabine, acyclovir, or vidarabine/acyclovir could not be isolated. These findings suggest that combinations with these antivirals, which are currently being evaluated singly for the therapy of severe forms of herpetic infection, could prove clinically useful if increasing numbers of resistant viral strains are observed.
不同浓度的阿昔洛韦与阿糖腺苷或其5'-单磷酸酯联合使用时,通常会在非洲绿猴肾细胞中与1型和2型单纯疱疹病毒的各种毒株产生相加作用。同样,这些药物的某些组合在降低接种2型单纯疱疹病毒的小鼠死亡率和延长平均死亡天数方面比单一药物更有效。在任何体外或体内组合中均未观察到拮抗作用或干扰作用。抗病毒活性的增加并非由药物的毒性作用所致。虽然对阿糖腺苷或阿昔洛韦耐药的病毒在细胞培养中很容易产生,但未获得交叉耐药的证据。此外,在两种药物存在的情况下,无法分离出对阿糖腺苷、阿昔洛韦或阿糖腺苷/阿昔洛韦耐药的突变体。这些发现表明,如果观察到耐药病毒株数量增加,目前正在单独评估用于治疗严重疱疹感染的这些抗病毒药物的联合使用可能在临床上有用。