A multivalent OMV vaccine induces broad protection against major Klebsiella pneumoniae disease-causing serotypes
The antigenic diversity of Klebsiella pneumoniae surface polysaccharides, O- and K-antigen, represents a significant challenge for developing broadly-acting vaccines. Here we report the development of Kp-OMV4, a multivalent outer membrane vesicle (OMV) vaccine incorporating the four predominant K. pneumoniae O-antigen serotypes responsible for most invasive disease worldwide. Kp-OMV4 elicits robust humoral and cellular immune responses, generating high-titer antibodies against both surface polysaccharides and conserved outer membrane proteins. Vaccine-induced antibodies display complement-mediated bactericidal activity against hypervirulent and multidrug-resistant clinical strains. In a murine sepsis model, immunization confers protection against lethal challenge and significantly reduces post-infection bacterial burden. Importantly, immune sera broadly recognize diverse clinical isolates, including strains expressing O- and K-antigen serotypes not included in the vaccine, supporting potential for broad strain coverage. This study indicates that the multicomponent nature of OMVs can be leveraged to overcome bacterial antigenic diversity and enable the development of vaccines with broad strain coverage. The authors report that a multivalent OMV vaccine against Klebsiella pneumoniae provides protection against lethal challenge with multiple strains in a mouse sepsis model, and induces antibodies that broadly recognize clinical isolates with diverse O- and K-antigen serotypes.
Authors
- Eva Gato (ORCID: https://orcid.org/0000-0002-1662-514X)
- Andrés Corral‐Lugo (ORCID: https://orcid.org/0000-0002-3452-4131)
- Astrid Pérez (ORCID: https://orcid.org/0000-0003-1809-3332)
- Ana Tajuelo (ORCID: https://orcid.org/0000-0001-8351-0943)
- Pedro Miguela-Villoldo (ORCID: https://orcid.org/0000-0002-8926-658X)
- Félix Docando (ORCID: https://orcid.org/0000-0001-8835-9349)
- J. Cañada (ORCID: https://orcid.org/0000-0002-8964-0551)
- Antonio J. Martín-Galiano (ORCID: https://orcid.org/0000-0002-6662-329X)
- Diego Megı́as (ORCID: https://orcid.org/0000-0003-0755-0518)
- María Carmen Terrón
- Alberto Peláez‐García (ORCID: https://orcid.org/0000-0002-5401-3216)
- Michael J. McConnell (ORCID: https://orcid.org/0000-0003-1028-381X)
- Maria Dolores Pérez-Vázquez (ORCID: https://orcid.org/0000-0003-0745-8914)
- Beatriz Cano‐Castaño (ORCID: https://orcid.org/0000-0001-7875-7781)
- Sonia Prieto Martín-Gil (ORCID: https://orcid.org/0009-0004-2577-6590)
Institutions
- University of Notre Dame (US)
- Centre National de la Recherche Scientifique (FR)
- Universidad Nacional de Educación a Distancia (ES)
- Instituto de Salud Carlos III (ES)
- Centro Nacional de Microbiologia (ES)
- Centro de Investigación Biomédica en Red (ES)
- Red Espanola de Investigacion en Patologia Infecciosa (ES)
- Institut de génétique et de développement de Rennes (FR)
- Centro de Investigación Biomédica en Red Enfermedades Infecciosas (ES)
- Université de Rennes (FR)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-11-02
- DOI
- https://doi.org/10.1038/s41467-026-78859-1
- Primary Topic
- Bacterial Infections and Vaccines
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Instituto de Salud Carlos III