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Cross-protective antibodies against common endemic respiratory viruses

Author

Listed:
  • Madelyn Cabán

    (Fred Hutchinson Cancer Center
    University of Washington)

  • Justas V. Rodarte

    (Fred Hutchinson Cancer Center)

  • Madeleine Bibby

    (Fred Hutchinson Cancer Center)

  • Matthew D. Gray

    (Fred Hutchinson Cancer Center)

  • Justin J. Taylor

    (Fred Hutchinson Cancer Center
    University of Washington)

  • Marie Pancera

    (Fred Hutchinson Cancer Center)

  • Jim Boonyaratanakornkit

    (Fred Hutchinson Cancer Center
    University of Washington)

Abstract

Respiratory syncytial virus (RSV), human metapneumovirus (HMPV), and human parainfluenza virus types one (HPIV1) and three (HPIV3) can cause severe disease and death in immunocompromised patients, the elderly, and those with underlying lung disease. A protective monoclonal antibody exists for RSV, but clinical use is limited to high-risk infant populations. Hence, therapeutic options for these viruses in vulnerable patient populations are currently limited. Here, we present the discovery, in vitro characterization, and in vivo efficacy testing of two cross-neutralizing monoclonal antibodies, one targeting both HPIV3 and HPIV1 and the other targeting both RSV and HMPV. The 3 × 1 antibody is capable of targeting multiple parainfluenza viruses; the MxR antibody shares features with other previously reported monoclonal antibodies that are capable of neutralizing both RSV and HMPV. We obtained structures using cryo-electron microscopy of these antibodies in complex with their antigens at 3.62 Å resolution for 3 × 1 bound to HPIV3 and at 2.24 Å for MxR bound to RSV, providing a structural basis for in vitro binding and neutralization. Together, a cocktail of 3 × 1 and MxR could have clinical utility in providing broad protection against four of the respiratory viruses that cause significant morbidity and mortality in at-risk individuals.

Suggested Citation

  • Madelyn Cabán & Justas V. Rodarte & Madeleine Bibby & Matthew D. Gray & Justin J. Taylor & Marie Pancera & Jim Boonyaratanakornkit, 2023. "Cross-protective antibodies against common endemic respiratory viruses," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36459-3
    DOI: 10.1038/s41467-023-36459-3
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    References listed on IDEAS

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    1. Aimin Tang & Zhifeng Chen & Kara S. Cox & Hua-Poo Su & Cheryl Callahan & Arthur Fridman & Lan Zhang & Sangita B. Patel & Pedro J. Cejas & Ryan Swoyer & Sinoeun Touch & Michael P. Citron & Dhanasekaran, 2019. "A potent broadly neutralizing human RSV antibody targets conserved site IV of the fusion glycoprotein," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    2. Davide Corti & Siro Bianchi & Fabrizia Vanzetta & Andrea Minola & Laurent Perez & Gloria Agatic & Barbara Guarino & Chiara Silacci & Jessica Marcandalli & Benjamin J. Marsland & Antonio Piralla & Elen, 2013. "Cross-neutralization of four paramyxoviruses by a human monoclonal antibody," Nature, Nature, vol. 501(7467), pages 439-443, September.
    3. Michael B. Battles & Vicente Más & Eduardo Olmedillas & Olga Cano & Mónica Vázquez & Laura Rodríguez & José A. Melero & Jason S. McLellan, 2017. "Structure and immunogenicity of pre-fusion-stabilized human metapneumovirus F glycoprotein," Nature Communications, Nature, vol. 8(1), pages 1-11, December.
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    1. Nicole V. Johnson & Revina C. Scherpenzeel & Mark J. G. Bakkers & Ajit R. Ramamohan & Daan Overveld & Lam Le & Johannes P. M. Langedijk & Joost A. Kolkman & Jason S. McLellan, 2024. "Structural basis for potent neutralization of human respirovirus type 3 by protective single-domain camelid antibodies," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    2. Tara C. Marcink & Gillian Zipursky & Elizabeth B. Sobolik & Kate Golub & Emily Herman & Kyle Stearns & Alexander L. Greninger & Matteo Porotto & Anne Moscona, 2024. "How a paramyxovirus fusion/entry complex adapts to escape a neutralizing antibody," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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