Yang Bingyi, Gostic Katelyn M, Adam Dillon C, Zhang Ru, Einav Tal, Peng Liping, Wong Sook San, Tsang Tim K, Cummings Derek A T, Sullivan Sheena G, Cobey Sarah, Cowling Benjamin J
WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Department of Ecology and Evolution, University of Chicago, Chicago, IL, USA.
Nat Microbiol. 2025 Jun 10. doi: 10.1038/s41564-025-02033-4.
Influenza virus infections generate antibodies that cross-react with antigenically similar viruses. However, the breadth of cross-reactivity is unclear. Here we analysed 200,000 haemagglutination inhibition (HAI) titrations from ferrets singly infected with A(H3N2) or A(H1N1)pdm09. We identified consistent influenza A virus subtype-specific patterns where breadth of HAI antibody cross-reactivity was associated with isolation time between tested and immunizing viruses. This was independent of virus strains, passage history and genetic mutations. A 6-year interval between virus isolation resulted in minimal HAI titres for A(H3N2), while A(H1N1)pdm09 demonstrated broader cross-reactivity with moderate titre reductions over the same interval. Analysis of HA substitutions revealed more amino acid substitutions between viruses for A(H3N2) and a greater reduction in HAI titres per substitution compared with A(H1N1). Longitudinal analysis of human antisera across age groups suggests that repeat A(H3N2) exposure increased HAI responses within the cross-reactivity range, with greater increases for more recent viruses. These results provide a framework for antigenically evolving pathogens such as influenza viruses.
流感病毒感染会产生与抗原相似病毒发生交叉反应的抗体。然而,交叉反应的广度尚不清楚。在此,我们分析了200,000次来自单独感染A(H3N2)或A(H1N1)pdm09的雪貂的血凝抑制(HAI)滴定数据。我们确定了一致的甲型流感病毒亚型特异性模式,其中HAI抗体交叉反应的广度与测试病毒和免疫病毒之间的分离时间相关。这与病毒株、传代历史和基因突变无关。病毒分离间隔6年导致A(H3N2)的HAI滴度极低,而A(H1N1)pdm09在相同间隔内表现出更广泛的交叉反应,滴度适度降低。对血凝素(HA)替换的分析表明,与A(H1N1)相比,A(H3N2)病毒之间的氨基酸替换更多,每次替换导致的HAI滴度降低幅度更大。对不同年龄组人类抗血清的纵向分析表明,反复接触A(H3N2)会增加交叉反应范围内的HAI反应,对较新病毒的增加幅度更大。这些结果为流感病毒等抗原不断演变的病原体提供了一个框架。