McCord R S, Breinig M K, Morahan P S
Antimicrob Agents Chemother. 1976 Jul;10(1):28-33. doi: 10.1128/AAC.10.1.28.
The immunomodulator pyran markedly protected 5-week-old mice from lethal intravenous infection with herpes simplex virus type 2. The 50% lethal dose was increased almost 100-fold in pyran-treated mice as compared with controls. Although the protection was not as marked in older mice (10 and 16 weeks old), there was a significant increase in mean survival time. When the pathogenesis of herpesvirus disease was monitored in control and drug-treated mice, the effect of pyran was most evident in the spinal cord, where virus was recovered from 20 of 25 control mice and from only 6 of 25 pyran-treated mice. There was also a significant reduction in the titer of virus present, and virus appeared later in the spinal cord of pyran-treated mice than in control mice. The protective effect of pyran was observed only when the drug was administered 24 h before viral challenge, was seen after both intraperitoneal and intravenous injection, and was not due to direct inactivation of the virus.
免疫调节剂吡喃能显著保护5周龄小鼠免受2型单纯疱疹病毒致死性静脉感染。与对照组相比,经吡喃处理的小鼠50%致死剂量增加了近100倍。虽然在年龄较大的小鼠(10周龄和16周龄)中保护作用不那么明显,但平均存活时间有显著增加。当在对照小鼠和药物处理小鼠中监测疱疹病毒病的发病机制时,吡喃的作用在脊髓中最为明显,25只对照小鼠中有20只脊髓中可检测到病毒,而25只经吡喃处理的小鼠中只有6只脊髓中可检测到病毒。同时,病毒滴度也显著降低,且吡喃处理小鼠脊髓中病毒出现的时间比对照小鼠晚。吡喃的保护作用仅在病毒攻击前24小时给药时才观察到,腹腔注射和静脉注射后均可见到这种保护作用,且该保护作用并非由于病毒的直接失活。