Sialic acid-anchored haemagglutinin stalk neutralizing antibody M-SiaB enhances protection against highly pathogenic influenza H5N1/Texas/2024

The recently emerged cattle H5N1/Texas/2024 strain highlights the need for effective prophylactic and therapeutic drug interventions, yet most existing neutralizing antibodies (NAbs) have limited efficacy against genetically divergent pathogenic influenza viruses. Here we engineer a sialic acid-anchored tandem M-SiaB by fusing a hemagglutinin (HA) stalk-specific monoclonal NAb with a sialic acid-receptor-binding domain (SiaB). M-SiaB shows 4- to 20-fold greater neutralizing potency against diverse authentic influenza viruses compared to the parental NAb and suppresses multiple stages of the viral life cycle, including viral attachment, entry and release. Importantly, intranasal M-SiaB confers markedly enhanced protection against nasal challenges with the pathogenic H1N1/PR8 and H5N1/Texas/2024 strains. Notably, a single dose of M‑SiaB maintains survival after a highly lethal H5N1/Texas/2024 challenge for up to 21 days. These findings demonstrate that simultaneously targeting HA stalk and sialic acid-receptor is a promising strategy to enhance the potency and breadth of NAbs against genetically divergent pathogenic influenza viruses.

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Publication Details

Journal
Nature Communications
Published
2026-06-29
DOI
https://doi.org/10.1038/s41467-026-74633-5
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Sialic acid-anchored haemagglutinin stalk neutralizing antibody M-SiaB enhances protection against highly pathogenic influenza H5N1/Texas/2024

Vincent Kwok‐Man Poon, Chris Chung‐Sing Chan, Yelim Lee, Runhong Zhou et al.
Nature Communications
Influenza Virus Research Studies
article

Sialic acid-anchored haemagglutinin stalk neutralizing antibody M-SiaB enhances protection against highly pathogenic influenza H5N1/Texas/2024

Vincent Kwok‐Man Poon, Chris Chung‐Sing Chan, Yelim Lee, Runhong Zhou, Jasper Fuk‐Woo Chan, Dongyan Zhou, Pui Wang, Kwok‐Yung Yuen, Ruina Jin, Na Liu, Kyungmin Kim, Li Liu, Yuting Chen, Zhiwei Chen, Honglin Chen, Lucetta Joselyn, Aruzhan Aldungarova
article en

Abstract

The recently emerged cattle H5N1/Texas/2024 strain highlights the need for effective prophylactic and therapeutic drug interventions, yet most existing neutralizing antibodies (NAbs) have limited efficacy against genetically divergent pathogenic influenza viruses. Here we engineer a sialic acid-anchored tandem M-SiaB by fusing a hemagglutinin (HA) stalk-specific monoclonal NAb with a sialic acid-receptor-binding domain (SiaB). M-SiaB shows 4- to 20-fold greater neutralizing potency against diverse authentic influenza viruses compared to the parental NAb and suppresses multiple stages of the viral life cycle, including viral attachment, entry and release. Importantly, intranasal M-SiaB confers markedly enhanced protection against nasal challenges with the pathogenic H1N1/PR8 and H5N1/Texas/2024 strains. Notably, a single dose of M‑SiaB maintains survival after a highly lethal H5N1/Texas/2024 challenge for up to 21 days. These findings demonstrate that simultaneously targeting HA stalk and sialic acid-receptor is a promising strategy to enhance the potency and breadth of NAbs against genetically divergent pathogenic influenza viruses.

Nature Communications
Hong Kong Baptist University (HK), Chinese University of Hong Kong (HK), Changzhi Medical College (CN), Hong Kong Science and Technology Parks Corporation (HK), University of Hong Kong - Shenzhen Hospital (CN), HKU-Pasteur Research Pole (HK), University of Hong Kong (HK)
Wellcome Trust, Innovation and Technology Commission, University of Hong Kong, National Science and Technology Major Project, Health and Medical Research Fund
Responsible consumption and production
Openalex Percentile: Top 8%
Influenza Virus Research Studies
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