Department of Ecology and Evolution, University of Chicago, Chicago, IL, USA.
Enteric Diseases Group, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Nat Commun. 2021 Jul 14;12(1):4313. doi: 10.1038/s41467-021-24566-y.
How a history of influenza virus infections contributes to protection is not fully understood, but such protection might explain the contrasting age distributions of cases of the two lineages of influenza B, B/Victoria and B/Yamagata. Fitting a statistical model to those distributions using surveillance data from New Zealand, we found they could be explained by historical changes in lineage frequencies combined with cross-protection between strains of the same lineage. We found additional protection against B/Yamagata in people for whom it was their first influenza B infection, similar to the immune imprinting observed in influenza A. While the data were not informative about B/Victoria imprinting, B/Yamagata imprinting could explain the fewer B/Yamagata than B/Victoria cases in cohorts born in the 1990s and the bimodal age distribution of B/Yamagata cases. Longitudinal studies can test if these forms of protection inferred from historical data extend to more recent strains and other populations.
流感病毒感染史如何促成保护作用尚不完全清楚,但这种保护作用可能解释了乙型流感病毒的两个谱系 B/Victoria 和 B/Yamagata 的病例在年龄分布上的差异。我们利用来自新西兰的监测数据,通过拟合统计模型对这些分布进行分析,发现它们可以用谱系频率的历史变化以及同一谱系株之间的交叉保护来解释。我们发现,对于首次感染 B/Yamagata 的人,存在针对 B/Yamagata 的额外保护,类似于在甲型流感中观察到的免疫印迹。虽然数据无法说明 B/Victoria 的免疫印迹情况,但 B/Yamagata 的免疫印迹可以解释 90 年代出生的人群中 B/Yamagata 病例比 B/Victoria 病例少,以及 B/Yamagata 病例的双峰年龄分布。纵向研究可以检验从历史数据推断出的这些保护形式是否适用于最近的菌株和其他人群。