AI Article Synopsis

  • Most traditional bacterial vaccines target specific strains or need modifications before development.
  • This new injectable biomaterial vaccine enhances immune responses by utilizing dendritic cells and combines regulatory-approved components to effectively capture and present bacterial antigens.
  • It has shown success in protecting mice and pigs from various severe bacterial infections, indicating potential for quick manufacturing and safe deployment during bacterial outbreaks or biothreat scenarios.

Article 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.

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Source
http://dx.doi.org/10.1038/s41551-021-00756-3DOI Listing

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