Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Microbiology, Faculty of Medical Sciences, National Autonomous University of Nicaragua, León 21000, Nicaragua.
Viruses. 2022 Sep 16;14(9):2053. doi: 10.3390/v14092053.
There are significant challenges to the development of a pediatric norovirus vaccine, mainly due to the antigenic diversity among strains infecting young children. Characterizing human norovirus serotypes and understanding norovirus immunity in naïve children would provide key information for designing rational vaccine platforms. In this study, 26 Nicaraguan children experiencing their first norovirus acute gastroenteritis (AGE) episode during the first 18 months of life were investigated. We used a surrogate neutralization assay that measured antibodies blocking the binding of 13 different norovirus virus-like particles (VLPs) to histo-blood group antigens (HBGAs) in pre- and post-infection sera. To assess for asymptomatic norovirus infections, stools from asymptomatic children were collected monthly, screened for norovirus by RT-qPCR and genotyped by sequencing. Seroconversion of an HBGA-blocking antibody matched the infecting genotype in 25 (96%) of the 26 children. A subset of 13 (50%) and 4 (15%) of the 26 children experienced monotypic GII and GI seroconversion, respectively, strongly suggesting a type-specific response in naïve children, and 9 (35%) showed multitypic seroconversion. The most frequent pairing in multitypic seroconversion (8/12) were GII.4 Sydney and GII.12 noroviruses, both co-circulating at the time. Blocking antibody titers to these two genotypes did not correlate with each other, suggesting multiple exposure rather than cross-reactivity between genotypes. In addition, GII titers remained consistent for at least 19 months post-infection, demonstrating durable immunity. In conclusion, the first natural norovirus gastroenteritis episodes in these young children were dominated by a limited number of genotypes and induced responses of antibodies blocking binding of norovirus VLPs in a genotype-specific manner, suggesting that an effective pediatric norovirus vaccine likely needs to be multivalent and include globally dominant genotypes. The duration of protection from natural infections provides optimism for pediatric norovirus vaccines administered early in life.
开发小儿诺如病毒疫苗存在重大挑战,主要是因为感染幼儿的病毒株具有抗原多样性。对人类诺如病毒血清型进行表征并了解初感儿童的诺如病毒免疫情况,可为设计合理的疫苗平台提供关键信息。在这项研究中,我们调查了 26 名在生命的头 18 个月中首次经历小儿诺如病毒急性肠胃炎(AGE)的尼加拉瓜儿童。我们使用了一种替代中和测定法,该方法可测量针对 13 种不同诺如病毒病毒样颗粒(VLPs)与组织血型抗原(HBGA)结合的抗体的阻断作用,该测定法在感染前和感染后血清中进行。为了评估无症状诺如病毒感染,我们每月从无症状儿童的粪便中采集样本,通过 RT-qPCR 筛查诺如病毒,并通过测序对其进行基因分型。在 26 名儿童中,25 名(96%)的血清抗体针对 HBGA 的阻断作用与感染的基因型相匹配。26 名儿童中有 13 名(50%)和 4 名(15%)分别经历了单型 GII 和 GI 血清转化,这强烈表明初感儿童具有针对特定类型的反应,9 名(35%)显示了多型血清转化。多型血清转化中最常见的配对(8/12)是 GII.4 Sydney 和 GII.12 诺如病毒,这两种病毒均在当时同时流行。针对这两种基因型的阻断抗体滴度彼此之间没有相关性,表明是多种暴露而不是基因型之间的交叉反应。此外,GII 滴度在感染后至少 19 个月内保持一致,表明具有持久免疫力。综上所述,这些幼儿的首次自然诺如病毒肠胃炎发作主要由少数几种基因型主导,并以基因型特异性的方式诱导了阻断诺如病毒 VLPs 结合的抗体反应,这表明有效的小儿诺如病毒疫苗可能需要是多价的,并包括全球流行的基因型。从自然感染中获得的保护持续时间为在生命早期接种小儿诺如病毒疫苗提供了乐观的前景。