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Aerosol delivery of SARS-CoV-2 human monoclonal antibodies in macaques limits viral replication and lung pathology

Author

Listed:
  • Daniel N. Streblow

    (Oregon Health & Science University)

  • Alec J. Hirsch

    (Oregon Health & Science University)

  • Jeffrey J. Stanton

    (Oregon Health & Science University)

  • Anne D. Lewis

    (Oregon Health & Science University)

  • Lois Colgin

    (Oregon Health & Science University)

  • Ann J. Hessell

    (Oregon Health & Science University)

  • Craig N. Kreklywich

    (Oregon Health & Science University)

  • Jessica L. Smith

    (Oregon Health & Science University)

  • William F. Sutton

    (Oregon Health & Science University)

  • David Chauvin

    (Aridis Pharmaceuticals)

  • Jennifer Woo

    (Aridis Pharmaceuticals)

  • Benjamin N. Bimber

    (Oregon Health & Science University)

  • Cierra N. LeBlanc

    (Oregon Health & Science University)

  • Sonia N. Acharya

    (Oregon Health & Science University)

  • Brian J. O’Roak

    (Oregon Health & Science University)

  • Harjinder Sardar

    (Oregon Health & Science University)

  • Mohammad M. Sajadi

    (VA Maryland Health Care System)

  • Zahra R. Tehrani

    (University of Maryland)

  • Mark R. Walter

    (University of Alabama at Birmingham)

  • Luis Martinez-Sobrido

    (Texas Biomedical Research Institute)

  • James J. Kobie

    (University of Alabama at Birmingham)

  • Rachel J. Reader

    (University of California)

  • Katherine J. Olstad

    (University of California)

  • Theodore R. Hobbs

    (Oregon Health & Science University)

  • Erica Ollmann Saphire

    (La Jolla Institute for Immunology)

  • Sharon L. Schendel

    (La Jolla Institute for Immunology)

  • Robert H. Carnahan

    (Vanderbilt University Medical Center)

  • Jonas Knoch

    (PARI Pharma GmbH)

  • Luis M. Branco

    (Zalgen Labs, LLC)

  • James E. Crowe

    (Vanderbilt University Medical Center)

  • Koen K. A. Rompay

    (University of California)

  • Phillip Lovalenti

    (Aridis Pharmaceuticals)

  • Truong

    (Aridis Pharmaceuticals)

  • Donald N. Forthal

    (University of California, Irvine, School of Medicine)

  • Nancy L. Haigwood

    (Oregon Health & Science University)

Abstract

Passively administered monoclonal antibodies (mAbs) given before or after viral infection can prevent or blunt disease. Here, we examine the efficacy of aerosol mAb delivery to prevent infection and disease in rhesus macaques inoculated with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant via intranasal and intratracheal routes. SARS-CoV-2 human mAbs or a human mAb directed to respiratory syncytial virus (RSV) are nebulized and delivered using positive airflow via facemask to sedated macaques pre- and post-infection. Nebulized human mAbs are detectable in nasal, oropharyngeal, and bronchoalveolar lavage (BAL) samples. SARS-CoV-2 mAb treatment significantly reduces levels of SARS-CoV-2 viral RNA and infectious virus in the upper and lower respiratory tracts relative to controls. Reductions in lung and BAL virus levels correspond to reduced BAL inflammatory cytokines and lung pathology. Aerosolized antibody therapy for SARS-CoV-2 could be effective for reducing viral burden and limiting disease severity.

Suggested Citation

  • Daniel N. Streblow & Alec J. Hirsch & Jeffrey J. Stanton & Anne D. Lewis & Lois Colgin & Ann J. Hessell & Craig N. Kreklywich & Jessica L. Smith & William F. Sutton & David Chauvin & Jennifer Woo & Be, 2023. "Aerosol delivery of SARS-CoV-2 human monoclonal antibodies in macaques limits viral replication and lung pathology," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42440-x
    DOI: 10.1038/s41467-023-42440-x
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