Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Viral Gastroenteritis Branch, Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J Infect Dis. 2024 May 15;229(5):1460-1469. doi: 10.1093/infdis/jiad403.
Even moderate differences in rotavirus vaccine effectiveness against nonvaccine genotypes may exert selective pressures on circulating rotaviruses. Whether this vaccine effect or natural temporal fluctuations underlie observed changes in genotype distributions is unclear.
We systematically reviewed studies reporting rotavirus genotypes from children <5 years of age globally between 2005 and 2023. We compared rotavirus genotypes between vaccine-introducing and nonintroducing settings globally and by World Health Organization (WHO) region, calendar time, and time since vaccine introduction.
Crude pooling of genotype data from 361 studies indicated higher G2P[4], a nonvaccine genotype, prevalence in vaccine-introducing settings, both globally and by WHO region. This difference did not emerge when examining genotypes over time in the Americas, the only region with robust longitudinal data. Relative to nonintroducing settings, G2P[4] detections were more likely in settings with recent introduction (eg, 1-2 years postintroduction adjusted odds ratio [aOR], 4.39; 95% confidence interval [CI], 2.87-6.72) but were similarly likely in settings with more time elapsed since introduction, (eg, 7 or more years aOR, 1.62; 95% CI, .49-5.37).
When accounting for both regional and temporal trends, there was no substantial evidence of long-term vaccine-related selective pressures on circulating genotypes. Increased prevalence of G2P[4] may be transient after rotavirus vaccine introduction.
即使轮状病毒疫苗对非疫苗基因型的有效性存在适度差异,也可能对循环轮状病毒施加选择压力。观察到的基因型分布变化是疫苗效果还是自然时间波动的结果尚不清楚。
我们系统地回顾了 2005 年至 2023 年间全球范围内报告的 5 岁以下儿童轮状病毒基因型的研究。我们比较了全球以及世界卫生组织(WHO)区域、日历时间和疫苗引入时间后引入和非引入环境中的轮状病毒基因型。
来自 361 项研究的基因型数据的粗略汇总表明,在全球和按 WHO 区域划分的疫苗引入环境中,非疫苗基因型 G2P[4]的流行率更高。当在美洲(唯一具有可靠纵向数据的地区)检查随时间变化的基因型时,这种差异并未出现。与非引入环境相比,在最近引入疫苗的环境中(例如,引入后 1-2 年,调整后的优势比[aOR]为 4.39;95%置信区间[CI]为 2.87-6.72),更有可能检测到 G2P[4],但在引入疫苗时间较长的环境中(例如,7 年或更长时间,aOR 为 1.62;95%CI 为.49-5.37),也有相似的可能性。
在考虑到区域和时间趋势的情况下,没有充分的证据表明循环基因型存在长期的疫苗相关选择压力。轮状病毒疫苗引入后,G2P[4]的流行率可能会暂时增加。