Krasnoproshina L I, Kil'diushevskaia T V, Serova T A, Vlasov G S, Dzhikidze E K, Balaeva E Ia, Voskanian N A, Alliluev A P, Kuvakina V I, Basnak'ian I A
Zh Mikrobiol Epidemiol Immunobiol. 1990 Oct(10):84-9.
The comparative study of two group B meningococcal vaccines manufactured in the USSR and in Cuba was made. The vaccine manufactured in the USSR contained the noncovalent compound of group B Neisseria meningitidis polysaccharide and outer membrane protein, and the Cuban vaccine contained group B N. meningitidis outer membrane proteins and group C N. meningitidis polysaccharide. The data obtained in this study indicated that both vaccines possessed immunological potency evaluated according to their capacity to stimulate the formation of bactericidal antibodies, whose level was found to increase eightfold after the immunization of monkeys in two injections. Besides, group B meningococcal vaccines did not induce the suppression of nonspecific protective activity characteristics of the body and did not stimulate the formation of autoantibodies to brain and liver tissues, which was indicative of the safety of these vaccines.
对苏联和古巴生产的两种B群脑膜炎球菌疫苗进行了对比研究。苏联生产的疫苗含有B群脑膜炎奈瑟菌多糖与外膜蛋白的非共价化合物,古巴疫苗含有B群脑膜炎奈瑟菌外膜蛋白和C群脑膜炎奈瑟菌多糖。本研究获得的数据表明,两种疫苗均具有免疫效力,根据其刺激杀菌抗体形成的能力进行评估,在给猴子分两次注射进行免疫后,杀菌抗体水平提高了八倍。此外,B群脑膜炎球菌疫苗不会导致机体非特异性保护活性特征受到抑制,也不会刺激针对脑和肝组织的自身抗体形成,这表明这些疫苗是安全的。