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Broadly-neutralizing antibodies that bind to the influenza hemagglutinin stalk domain enhance the effectiveness of neuraminidase inhibitors via Fc-mediated effector functions

Ali Zhang, Hanu Chaudhari, Yonathan Agung, Michael R. D’Agostino, Jann C. Ang, Matthew S. Miller
doi: https://doi.org/10.1101/2021.11.17.468248
Ali Zhang
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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Hanu Chaudhari
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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Yonathan Agung
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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Michael R. D’Agostino
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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Jann C. Ang
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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Matthew S. Miller
1Michael G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada, L8S 4K1
2McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada, L8S 4K1
3Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8S 4K1
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  • For correspondence: mmiller@mcmaster.ca
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Summary

The conserved hemagglutinin stalk domain is an attractive target for broadly effective antibody-based therapeutics and next generation universal influenza vaccines. Protection provided by hemagglutinin stalk binding antibodies is principally mediated through activation of immune effector cells. Titers of stalk-binding antibodies are highly variable on an individual level, and tend to increase with age as a result of increasing exposures to influenza virus. In our study, we show that stalk-binding antibodies cooperate with neuraminidase inhibitors to protect against influenza virus infection in an Fc-dependent manner. These data suggest that the effectiveness of neuraminidase inhibitors is likely influenced by an individual’s titers of stalk-binding antibodies, and that neuraminidase inhibitors may enhance the effectiveness of future stalk-binding monoclonal antibody-based treatments.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 19, 2021.
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Broadly-neutralizing antibodies that bind to the influenza hemagglutinin stalk domain enhance the effectiveness of neuraminidase inhibitors via Fc-mediated effector functions
Ali Zhang, Hanu Chaudhari, Yonathan Agung, Michael R. D’Agostino, Jann C. Ang, Matthew S. Miller
bioRxiv 2021.11.17.468248; doi: https://doi.org/10.1101/2021.11.17.468248
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Broadly-neutralizing antibodies that bind to the influenza hemagglutinin stalk domain enhance the effectiveness of neuraminidase inhibitors via Fc-mediated effector functions
Ali Zhang, Hanu Chaudhari, Yonathan Agung, Michael R. D’Agostino, Jann C. Ang, Matthew S. Miller
bioRxiv 2021.11.17.468248; doi: https://doi.org/10.1101/2021.11.17.468248

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