Biomaterial vaccines capturing pathogen-associated molecular patterns protect against bacterial infections and septic shock
- PMID: 34239117
- DOI: 10.1038/s41551-021-00756-3
Biomaterial vaccines capturing pathogen-associated molecular patterns protect against bacterial infections and septic shock
Abstract
Most bacterial vaccines work for a subset of bacterial strains or require the modification of the antigen or isolation of the pathogen before vaccine development. Here we report injectable biomaterial vaccines that trigger potent humoral and T-cell responses to bacterial antigens by recruiting, reprogramming and releasing dendritic cells. The vaccines are assembled from regulatorily approved products and consist of a scaffold with absorbed granulocyte-macrophage colony-stimulating factor and CpG-rich oligonucleotides incorporating superparamagnetic microbeads coated with the broad-spectrum opsonin Fc-mannose-binding lectin for the magnetic capture of pathogen-associated molecular patterns from inactivated bacterial-cell-wall lysates. The vaccines protect mice against skin infection with methicillin-resistant Staphylococcus aureus, mice and pigs against septic shock from a lethal Escherichia coli challenge and, when loaded with pathogen-associated molecular patterns isolated from infected animals, uninfected animals against a challenge with different E. coli serotypes. The strong immunogenicity and low incidence of adverse events, a modular manufacturing process, and the use of components compatible with current good manufacturing practice could make this vaccine technology suitable for responding to bacterial pandemics and biothreats.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.
References
-
- Rice, L. B. Federal funding for the study of antimicrobial resistance in nosocomial pathogens: no ESKAPE. J. Infect. Dis. 197, 1079–1081 (2008). - DOI
-
- Spellberg, B. et al. The epidemic of antibiotic-resistant infections: a call to action for the medical community from the Infectious Diseases Society of America. Clin. Infect. Dis. 46, 155–164 (2008). - DOI
-
- Adalja, A. A. Biothreat agents and emerging infectious disease in the emergency department. Emerg. Med. Clin. North Am. 36, 823–834 (2018). - DOI
-
- Messner, P., Schaffer, C. & Kosma, P. Bacterial cell-envelope glycoconjugates. Adv. Carbohydr. Chem. Biochem. 69, 209–272 (2013). - DOI
-
- Haji-Ghassemi, O., Blackler, R. J., Martin Young, N. & Evans, S. V. Antibody recognition of carbohydrate epitopesdagger. Glycobiology 25, 920–952 (2015). - DOI
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