Gribencha S V, Litvin A A, Kokhnovich M A, Sergienko V I, Stovbun S V, Iakimuk P V, Bezmen V G
Antibiot Khimioter. 2009;54(5-6):31-6.
Significant and reliable activity of panavir was shown in experiments on mice intramuscularly infected with the rabies virus. The animal protection depended on the dose of panavir and the treatment scheme. The reliable protection (30-45% of the mice, p<0.05-0.01) was observed only after the panavir intramuscular injection to the site of the virus inoculation (the infection atrium), but not after the systemic (intraperitoneal) administration. High titers of the virus-neutralizing antibodies (7.92-10.45 IU/ml), comparable to the antibody titers in the combined suspensions of the brain tissues (6.01-10.45% IU/ml), were detected in the combined sera of the survived animals treated with panavir. For the first time a quantitative method for determination of the virus-neutralizing antibody levels in IU/ml was used (the FAVN test, the gold standard for comparative evaluation of the level of the vaccinal and infective antirabies immunity).
在对肌肉注射感染狂犬病病毒的小鼠进行的实验中,泛病毒显示出显著且可靠的活性。动物保护情况取决于泛病毒的剂量和治疗方案。仅在将泛病毒肌肉注射到病毒接种部位(感染灶)后,才观察到可靠的保护效果(30% - 45%的小鼠,p<0.05 - 0.01),而全身(腹腔内)给药后则未观察到。在用泛病毒治疗的存活动物的混合血清中,检测到高滴度的病毒中和抗体(7.92 - 10.45 IU/ml),与脑组织混合悬液中的抗体滴度(6.01 - 10.45 IU/ml)相当。首次使用了以IU/ml为单位测定病毒中和抗体水平的定量方法(FAVN试验,这是比较评估疫苗和感染性抗狂犬病免疫水平的金标准)。