{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T15:56:24Z","timestamp":1785426984702,"version":"3.56.0"},"posted":{"date-parts":[[2026,3,12]]},"group-title":"Immunology","reference-count":0,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T00:00:00Z","timestamp":1773273600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"award":["R01 AI165692"],"award-info":[{"award-number":["R01 AI165692"]}],"id":[{"id":"https:\/\/ror.org\/01cwqze88","id-type":"ROR","asserted-by":"publisher"}]},{"name":"Carl R. Woese Institute for Genomic Biology","award":["Carl R. Woese Institute for Genomic Biology Postdoctoral Fellowship"],"award-info":[{"award-number":["Carl R. Woese Institute for Genomic Biology Postdoctoral Fellowship"]}]},{"award":["Vallee Scholars Program"],"award-info":[{"award-number":["Vallee Scholars Program"]}],"id":[{"id":"https:\/\/ror.org\/05nmp3276","id-type":"ROR","asserted-by":"publisher"}]},{"award":["Searle Scholars Program"],"award-info":[{"award-number":["Searle Scholars Program"]}],"id":[{"id":"https:\/\/ror.org\/041nz5a71","id-type":"ROR","asserted-by":"publisher"}]},{"award":["Emerging Pathogens Initiative"],"award-info":[{"award-number":["Emerging Pathogens Initiative"]}],"id":[{"id":"https:\/\/ror.org\/006w34k90","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2026,3,12]]},"abstract":"<jats:p>While influenza A virus undergoes rapid antigenic drift in humans, at least some subtypes, such as H3, have relatively stable antigenicity in natural waterfowl reservoirs, despite the presence of immune pressure. However, the underlying mechanisms remain poorly understood. This study identified and characterized 187 antibodies to H3 hemagglutinin from experimentally infected mallard ducks, 18 of which were further analyzed by cryo-EM. Compared with human H3 antibodies, duck H3 antibodies exhibited higher glycan-binding propensity, more balanced immunodominance hierarchy, and targeted distinct epitopes. Other unique features of duck H3 antibodies included a convergent CDR H3-independent heavy chain-only binding mode and an N-glycosylated CDR H3 as decoy receptor. By annotating duck immunoglobulin germline genes, we also demonstrated the importance of gene conversion in duck H3 antibodies. 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