Research Department, Sanofi Pasteur Campus Merieux, 1541 avenue Marcel Merieux, 69680 Marcy l'Etoile, France.
Virology. 2012 Aug 1;429(2):91-8. doi: 10.1016/j.virol.2012.03.007. Epub 2012 Apr 25.
The objective of the study was to evaluate if the antibodies elicited after immunization with a tetravalent dengue vaccine, based on chimeric yellow fever 17D/dengue viruses, can neutralize a large range of dengue viruses (DENV). A panel of 82 DENVs was developed from viruses collected primarily during the last decade in 30 countries and included the four serotypes and the majority of existing genotypes. Viruses were isolated and minimally amplified before evaluation against a tetravalent polyclonal serum generated during vaccine preclinical evaluation in monkey, a model in which protection efficacy of this vaccine has been previously demonstrated (Guirakhoo et al., 2004). Neutralization was observed across all the DENV serotypes, genotypes, geographical origins and isolation years. These data indicate that antibodies elicited after immunization with this dengue vaccine candidate should widely protect against infection with contemporary DENV lineages circulating in endemic countries.
本研究的目的是评估基于嵌合黄热 17D/登革热病毒的四价登革热疫苗接种后产生的抗体是否能够中和大范围的登革热病毒(DENV)。该研究小组开发了一个包含 82 种登革热病毒的病毒组,这些病毒主要来自过去十年中 30 个国家的病毒收集,包括四个血清型和大多数现有的基因型。在针对在猴中进行疫苗临床前评估期间产生的四价多克隆血清进行评估之前,对病毒进行了分离和最小程度的扩增,在该模型中,该疫苗的保护功效已得到证实(Guirakhoo 等人,2004 年)。观察到所有 DENV 血清型、基因型、地理起源和分离年份的中和作用。这些数据表明,用这种候选登革热疫苗免疫后产生的抗体应该能够广泛保护免受流行国家中循环的当代 DENV 谱系的感染。