1. Academic Validation
  2. Cross-protective antibodies against common endemic respiratory viruses

Cross-protective antibodies against common endemic respiratory viruses

  • Nat Commun. 2023 Feb 13;14(1):798. doi: 10.1038/s41467-023-36459-3.
Madelyn Cabán # 1 2 Justas V Rodarte # 1 Madeleine Bibby # 1 Matthew D Gray 1 Justin J Taylor 3 4 Marie Pancera 5 Jim Boonyaratanakornkit 6 7
Affiliations

Affiliations

  • 1 Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • 2 Department of Immunology & Department of Global Health, University of Washington, Seattle, WA, USA.
  • 3 Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. [email protected].
  • 4 Department of Immunology & Department of Global Health, University of Washington, Seattle, WA, USA. [email protected].
  • 5 Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. [email protected].
  • 6 Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. [email protected].
  • 7 Department of Medicine, University of Washington, Seattle, WA, USA. [email protected].
  • # Contributed equally.
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.

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