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用Vero细胞或原代猴肾细胞制备的两种口服脊髓灰质炎疫苗对婴儿进行接种后脊髓灰质炎病毒排泄情况的比较研究。

Comparative study of poliovirus excretion after vaccination of infants with two oral polio vaccines prepared on Vero cells or on primary monkey kidney cells.

作者信息

Mallet L, Pelloquin F, Brigaud M, Caudrelier P, Bandet R, Xueref C, Fuchs F, Gibelin N, Goldman C, Moulin J C, de Fraipont F, Montagnon B, Peyron L, Aymard M

机构信息

Pasteur Mérieux Sérums et Vaccins, Lyon, France.

出版信息

J Med Virol. 1997 May;52(1):50-60.

PMID:9131458
Abstract

A comparative study was designed to assess the bioequivalence of 2 oral poliovaccines (OPV) produced on 2 different cell systems: primary monkey kidney (PMK) cells and the Vero cell line. The Vero cell line has been used to overcome the problem of obtaining a regular supply of high quality monkeys that are devoid of latent viruses. For this study, 9 children were vaccinated with PMK-OPV and 12 children with Vero-OPV. The comparison covered poliovirus excretion, reversion of polioviruses in the 5'-noncoding region, and immunogenicity. Major molecular markers in the 5'-noncoding region related to neurovirulence already had been identified at position 480 for type 1, position 481 for type 2, and position 472 for type 3 poliovirus. Two nucleic-acid based methods were designed for studying these positions: a RT-PCR followed by sequencing, which required preliminary culture and cloning; and a type-specific nested PCR followed by sequencing, which enabled direct detection and genotyping of polioviruses. Twenty-eight stool specimens were analyzed by this second method with no PCR inhibition problem. The use of Vero cell line did not modify the global pattern of poliovirus excretion, reversion frequency, or seroconversion. These results provide additional support for the use of the well-characterized Vero cell line in OPV manufacturing.

摘要

设计了一项比较研究,以评估在两种不同细胞系统上生产的两种口服脊髓灰质炎疫苗(OPV)的生物等效性:原代猴肾(PMK)细胞和Vero细胞系。Vero细胞系已被用于克服获得稳定供应的无潜伏病毒的高质量猴子的问题。在本研究中,9名儿童接种了PMK-OPV,12名儿童接种了Vero-OPV。比较内容包括脊髓灰质炎病毒排泄、脊髓灰质炎病毒在5'-非编码区的回复突变以及免疫原性。与神经毒力相关的5'-非编码区主要分子标记,1型脊髓灰质炎病毒已确定位于480位,2型位于481位,3型位于472位。设计了两种基于核酸的方法来研究这些位置:一种是RT-PCR后测序,这需要初步培养和克隆;另一种是型特异性巢式PCR后测序,可直接检测脊髓灰质炎病毒并进行基因分型。用第二种方法分析了28份粪便标本,未出现PCR抑制问题。使用Vero细胞系并未改变脊髓灰质炎病毒排泄的总体模式、回复突变频率或血清转化情况。这些结果为在OPV生产中使用特性明确的Vero细胞系提供了更多支持。

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