Grachev V P, Karganova G G, Rumyantsev A A, Ivanova O E, Eremeeva T P, Drozdov S G
Chumakov Institute of Poliomyelitis and Viral Encephalitides RAMS, Moscow Region, Russia.
Dev Biol (Basel). 2001;105:211-7.
In the draft recommendations for production and control of OPV the WHO proposed new control methods: (i) mutant analysis with PCR and restriction enzyme cleavage (MAPREC) assay that allows evaluation of poliovirus population heterogeneity at the molecular level; (ii) neurovirulence (NV) test using transgenic mice susceptible to polioviruses and (iii) control of the seed lots for the presence of the simian virus 40 (SV40) DNA sequence. This paper is focused on our experience in the practical implementation of the new methods at the Institute of Poliomyelitis and Viral Encephalitides (IPVE). Using methods based on PCR we have demonstrated that working seed viruses used by IPVE for OPV production are free from SV40 DNA sequences. Our experience on the conduction of the OPV type 3 control using TgPVR21 mice NV test (seven vaccine lots) and the MAPREC assay (more than 150 samples of single harvests and monovalent bulks) showed that these methods may be used instead of the monkey NV test, because they could not pass the vaccine failed monkey NV test. The necessity for single harvests control is discussed.
在世界卫生组织关于口服脊髓灰质炎疫苗(OPV)生产和控制的建议草案中,提出了新的控制方法:(i)采用聚合酶链反应(PCR)和限制性内切酶切割的突变分析(MAPREC)检测法,该方法可在分子水平评估脊髓灰质炎病毒群体的异质性;(ii)使用对脊髓灰质炎病毒易感的转基因小鼠进行神经毒力(NV)测试;以及(iii)检测种子批中是否存在猴病毒40(SV40)DNA序列。本文重点介绍了我们在脊髓灰质炎和病毒性脑炎研究所(IPVE)实际应用这些新方法的经验。通过基于PCR的方法,我们证明了IPVE用于生产OPV的工作种子病毒不含SV40 DNA序列。我们使用TgPVR21小鼠NV测试(七批疫苗)和MAPREC检测法(超过150个单批收获物和单价原液样品)对3型OPV进行控制的经验表明,这些方法可替代猴NV测试,因为未能通过猴NV测试的疫苗也无法通过这些方法的检测。文中还讨论了对单批收获物进行控制的必要性。