Enhancing the breadth of protection in mice with a multivalent influenza vaccine

The high mutation rate of the influenza virus poses a significant challenge to global health, highlighting the urgent need for broad-spectrum vaccines. Here, we engineered Ad-Hex, a pan-influenza vaccine comprising three chimpanzee adenoviral vectors (Ad-H1H3, Ad-BYBV, and Ad-H5H7), each encoding the hemagglutinin (HA) genes from two distinct influenza virus subtypes/lineages in the △E1 region. A single intranasal dose of Ad-Hex induced robust humoral, cellular, and mucosal immunity, conferring complete protection against lethal challenge with six vaccine-matched strains in female C57BL/6 or Balb/c mice. Notably, the vaccine achieved 60% survival rates against mismatched strains. Mechanistic studies revealed that Ad-Hex activated germinal center B-cell responses not only against the cognate HAs but also against the conserved HA stalks. This drove the production of cross-reactive antibodies, which contributed to heterologous protection along with the CD8<sup>+</sup> T cell response. Our study confirms the feasibility of this multivalent strategy by mixing multiple recombinant adenoviruses and provides insights into the development of multivalent vaccines against other respiratory pathogens.

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Publication Details

Journal
Communications Biology
Published
2026-01-07
DOI
https://doi.org/10.1038/s42003-025-09451-4
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Enhancing the breadth of protection in mice with a multivalent influenza vaccine

Man Xing, Ping Zhou, Mangteng Wu, Longfei Ding et al.
Communications Biology
Influenza Virus Research Studies
article

Enhancing the breadth of protection in mice with a multivalent influenza vaccine

Man Xing, Ping Zhou, Mangteng Wu, Longfei Ding, Yao Yan, Miaomiao Zhang, Xiang Wang, Yixin Niu, Xi Yang, Ying Hu, Dongming Zhou, Caihong Zhu, Hongyang Shi, Shubing Tang
article en

Abstract

The high mutation rate of the influenza virus poses a significant challenge to global health, highlighting the urgent need for broad-spectrum vaccines. Here, we engineered Ad-Hex, a pan-influenza vaccine comprising three chimpanzee adenoviral vectors (Ad-H1H3, Ad-BYBV, and Ad-H5H7), each encoding the hemagglutinin (HA) genes from two distinct influenza virus subtypes/lineages in the △E1 region. A single intranasal dose of Ad-Hex induced robust humoral, cellular, and mucosal immunity, conferring complete protection against lethal challenge with six vaccine-matched strains in female C57BL/6 or Balb/c mice. Notably, the vaccine achieved 60% survival rates against mismatched strains. Mechanistic studies revealed that Ad-Hex activated germinal center B-cell responses not only against the cognate HAs but also against the conserved HA stalks. This drove the production of cross-reactive antibodies, which contributed to heterologous protection along with the CD8<sup>+</sup> T cell response. Our study confirms the feasibility of this multivalent strategy by mixing multiple recombinant adenoviruses and provides insights into the development of multivalent vaccines against other respiratory pathogens.

Communications BiologyVol. 9(1)
Chinese Academy of Sciences (CN), Shanghai Institutes for Biological Sciences (CN), Shanghai Public Health Clinical Center (CN), Shanghai Drug Administration (CN), Tianjin Medical University (CN)
National Natural Science Foundation of China, NIH Clinical Center
Good health and well-being
Openalex Percentile: Top 96%
Influenza Virus Research Studies
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