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Profiling Human Papillomavirus Lineage-Specific Capsid Antigenicity With Geographically Diverse Natural Infection Antibodies

  • Kavita Panwar
  • , Kazutomo Yokoya
  • , Sofia Gomes
  • , Vanessa Tenet
  • , John Schussler
  • , Rolando Herrero
  • , Lisa Mirabello
  • , John T. Schiller
  • , Mónica S. Sierra
  • , Gary M. Clifford
  • , Simon Beddows*
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

Human papillomavirus variants are classified into lineages based on their whole genome sequence, but the impact of lineage variation on the structure or function of encoded proteins is unclear. We used a global panel of lineage-specific natural infection sera to assess antibody-binding specificity for lineage-specific L1L2 antigens, and we used these data to create relational antigenic maps. Merging these data with neutralizing antibody data demonstrated similar spatial geometry and revealed dependency on a limited number of amino residues on the capsid surface. These data inform the degree of lineage specificity within the natural infection humoral immune response to oncogenic human papillomaviruses.

Original languageEnglish
Pages (from-to)e145-e150
JournalJournal of Infectious Diseases
Volume233
Issue number1
DOIs
Publication statusPublished - 1 Oct 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • HPV
  • antibody
  • antigen
  • lineage
  • natural infection

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