Selimov M, Aksenova T, Klyueva E, Gribencha L, Lebedeva I
Dev Biol Stand. 1978;40:57-62.
During 1973-1977, 981,000 doses of rabies vaccine were prepared in primary young Syrian hamster kidney cell cultures infected with attenuated rabies virus (strain Vnukovo-32) and inactivated by UV-irradiation. Potency of the vaccine varied from 0.3 to 3.5. More the 53% of vaccine lots had potency in the range of 1.1-3.5 (NIH). Post-exposure immunization was carried out in 45,842 persons aged from 2 weeks to greater than 76 years. The vaccination course lasted from 2 to 25 days and was followed by 2 booster injections with the dose of 1.5-5 ml. The vaccine combined with gammaglobulin was injected into 2,856 persons; 19,764 persons had bites of dangerous localization (face, head, fingers). Post-exposure immunization was carried out in 4,416 humans who were bitten or licked with saliva of rabid animals (diagnosis was confirmed clinically or in the laboratory) and in 16,760 humans bitten by suspected animals (diagnosis remained unknown). None of those who received the complete course of antirabic treatment fell ill with hydrophobia. No neurological complications or other severe side effects were noted. Field trials and the results of studies of virus-neutralizing antibody titers in 390 treated people make it possible to conclude that tissue culture rabies vaccine from strain Vnukovo-32 is an effective preparation with low reactogenicity.
1973年至1977年期间,用感染减毒狂犬病病毒(Vnukovo - 32株)并经紫外线照射灭活的原代幼年叙利亚仓鼠肾细胞培养物制备了98.1万剂狂犬病疫苗。疫苗效力在0.3至3.5之间。超过53%的疫苗批次效力在1.1 - 3.5范围内(美国国立卫生研究院标准)。对45842名年龄从2周至76岁以上的人群进行了暴露后免疫。接种疗程持续2至25天,随后进行2次剂量为1.5 - 5毫升的加强注射。将疫苗与丙种球蛋白联合注射给了2856人;19764人有危险部位(面部、头部、手指)的咬伤。对4416名被狂犬动物咬伤或舔舐(临床或实验室确诊)以及16760名被疑似动物咬伤(诊断不明)的人进行了暴露后免疫。接受完整抗狂犬病治疗疗程的人中无一例患狂犬病。未观察到神经并发症或其他严重副作用。现场试验以及对390名接受治疗者病毒中和抗体滴度的研究结果表明,Vnukovo - 32株组织培养狂犬病疫苗是一种反应原性低的有效制剂。