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Article: Breadth of influenza A antibody cross-reactivity varies by virus isolation interval and subtype

TitleBreadth of influenza A antibody cross-reactivity varies by virus isolation interval and subtype
Authors
Issue Date10-Jun-2025
PublisherSpringer Nature
Citation
Nature Microbiology, 2025, v. 10, p. 1711-1722 How to Cite?
AbstractInfluenza 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.
Persistent Identifierhttp://hdl.handle.net/10722/364066

 

DC FieldValueLanguage
dc.contributor.authorYang, Bingyi-
dc.contributor.authorGostic, Katelyn M.-
dc.contributor.authorAdam, Dillon C.-
dc.contributor.authorZhang, Ru-
dc.contributor.authorEinav, Tal-
dc.contributor.authorPeng, Liping-
dc.contributor.authorWong, Sook San-
dc.contributor.authorTsang, Tim K.-
dc.contributor.authorCummings, Derek A.T.-
dc.contributor.authorSullivan, Sheena G.-
dc.contributor.authorCobey, Sarah-
dc.contributor.authorCowling, Benjamin J.-
dc.date.accessioned2025-10-21T00:35:26Z-
dc.date.available2025-10-21T00:35:26Z-
dc.date.issued2025-06-10-
dc.identifier.citationNature Microbiology, 2025, v. 10, p. 1711-1722-
dc.identifier.urihttp://hdl.handle.net/10722/364066-
dc.description.abstractInfluenza 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.-
dc.languageeng-
dc.publisherSpringer Nature-
dc.relation.ispartofNature Microbiology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleBreadth of influenza A antibody cross-reactivity varies by virus isolation interval and subtype-
dc.typeArticle-
dc.identifier.doi10.1038/s41564-025-02033-4-
dc.identifier.scopuseid_2-s2.0-105007655172-
dc.identifier.volume10-
dc.identifier.spage1711-
dc.identifier.epage1722-
dc.identifier.eissn2058-5276-
dc.identifier.issnl2058-5276-

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