Fischer G W, Balk M W, Crumrine M H, Bass J W
J Infect Dis. 1976 Jun;133 Suppl:A217-20. doi: 10.1093/infdis/133.supplement_2.a217.
Encephalitis was induced in 10-day-old Wistar rats by intraperitoneal injection of approximately 100 50% tissue culture infective doses of herpes simplex virus type 2. Treatment regimens included immunopotentiation with levamisole and combined therapy with levamisole and an antiviral agent, adenine arabinoside. Rats treated with levamisole alone had significantly higher rates of survival than placebo-treated controls 14 days after injection of virus. Combination therapy with levamisole and adenine arabinoside prolonged survival, but there was no significant difference between treated animals and controls given placebo. Because adenine arabinoside inhibits the beneficial effect of levamisole in this model, antiviral chemotherapy in conjunction with immunopotentiation should be used with caution in humans. Further studies will be necessary to determine the value of immunopotentiation therapy in the treatment of life-threatening viral infections.
通过腹腔注射约100个50%组织培养感染剂量的2型单纯疱疹病毒,在10日龄的Wistar大鼠中诱发脑炎。治疗方案包括用左旋咪唑进行免疫增强以及左旋咪唑与抗病毒药物阿糖腺苷的联合治疗。单独用左旋咪唑治疗的大鼠在注射病毒14天后的存活率显著高于用安慰剂治疗的对照组。左旋咪唑与阿糖腺苷的联合治疗延长了存活时间,但治疗组动物与给予安慰剂的对照组之间没有显著差异。由于在该模型中阿糖腺苷会抑制左旋咪唑的有益作用,因此在人类中联合免疫增强进行抗病毒化疗时应谨慎使用。有必要进行进一步研究以确定免疫增强疗法在治疗危及生命的病毒感染中的价值。