Lalosević D, Lalosević V, Lazarević-Ivanc Lj, Knezević I
Faculty of Medicine, Pasteur Institute, Novi Sad, Serbia.
Dev Biol (Basel). 2008;131:421-9.
Veterinary rabies vaccines produced in BHK-21/C13 permanent cell cultures have been used for a long period of time and have been proven as efficacious and safe. A candidate vaccine for human use (YU BHK Rabivak) was developed at the Pasteur Institute, Novi Sad, Serbia on the basis of the fixed rabies virus strain "L. Pasteur 2061/Vero 15 pas" using BHK 21/C13 as a cell substrate for vaccine production. To test the vaccine immunogenicity, a clinical trial was conducted involving 164 subjects between 18 and 60 years of age, immunized either with the YU BHK Rabivak vaccine candidate orwith a commercially available vaccine (Rabipur). Three groups of subjects were immunized with either vaccine by intramuscular administration in the deltoid region, following a pre-exposure regimen on days 0, 7 and 21, or the Essen or Zagreb post-exposure regimens. Rabies virus neutralizing antibodies (VNA) titres were determined by rapid fluorescent focus inhibition test (RFFIT) 21 and 30-45 days post vaccination. A protective titre of VNAs (>0.5 IU/ml) was found in all subjects vaccinated. Dynamics of the immune response showed that 96.4% of the subjects developed protective VNA titres after two doses, 99.3% after three doses and 100% after four and five doses of the candidate YU BHK Rabivak vaccine. There was a low reactogenicity without serious adverse events indicating a satisfactory safety profile in humans. Results obtained in this study indicate that BHK 21 cells offer the possibility of producing an efficacious and safe cell-culture rabies vaccine for humane use.
在BHK - 21/C13永久细胞培养物中生产的兽用狂犬病疫苗已使用很长时间,并且已被证明有效且安全。塞尔维亚诺维萨德巴斯德研究所基于固定狂犬病病毒株“L. Pasteur 2061/Vero 15 pas”,以BHK 21/C13作为疫苗生产的细胞基质,开发了一种人用候选疫苗(YU BHK Rabivak)。为测试该疫苗的免疫原性,进行了一项临床试验,涉及164名年龄在18至60岁之间的受试者,他们分别接种YU BHK Rabivak候选疫苗或市售疫苗(Rabipur)。三组受试者通过在三角肌区域进行肌肉注射接种其中一种疫苗,按照0、7和21天的暴露前方案,或埃森或萨格勒布暴露后方案进行接种。在接种疫苗后21天以及30 - 45天,通过快速荧光灶抑制试验(RFFIT)测定狂犬病病毒中和抗体(VNA)滴度。在所有接种疫苗的受试者中均发现了保护性VNA滴度(>0.5 IU/ml)。免疫反应动态显示,96.4%的受试者在接种两剂后产生了保护性VNA滴度,99.3%在接种三剂后产生,100%在接种四剂和五剂候选YU BHK Rabivak疫苗后产生。反应原性较低,无严重不良事件,表明在人体中具有令人满意的安全性。本研究获得的结果表明,BHK 21细胞提供了生产一种有效且安全的人用细胞培养狂犬病疫苗的可能性。