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Modular biomaterials vaccine technology protects against multiple pathogens and septic shock

Super, M.; Doherty, E. J.; Cartwright, M. J.; Seiler, B. T.; White, D. A.; Langellotto, F.; Stafford, A. G.; Dimitrakakis, N.; Karkada, M.; Graveline, A. R.; Horgan, C. L.; Lightbown, K. R.; Urena, F. R.; Yeager, C. D.; Rifai, S. A.; Dellacherie, M. O.; Li, A. W.; Jiang, A. R.; Chandrasekhar, V.; Scott, J. M.; Lightbown, S. L.; Ingber, D. E.; Mooney, D. J.

2020-02-26 immunology
10.1101/2020.02.25.964601 bioRxiv
Show abstract

Broad spectrum vaccines could provide a solution to the emergence of antibiotic resistant microbes, pandemics and engineered biothreat agents. Here, we describe a modular vaccine (composite infection vaccine technology (ciVAX)) which can be rapidly assembled and in which 4 of the 5 components are already approved for human use. ciVAX consists of an injectable biomaterial scaffold with factors to recruit and activate dendritic cells (DC) in vivo and microbeads conjugated with the broad-spectrum opsonin Fc-Mannose-binding Lectin (FcMBL) that is pre-bound to polysaccharide-rich cell wall antigens, such as the pathogen-associated molecular patterns (PAMPs) fractions, captured from whole inactivated bacteria. Vaccination of mice and rabbits with ciVAX generates potent humoral and T cell responses to PAMPs isolated from native antibiotic-resistant E. coli and S. aureus, and ciVAX protects mice and pigs against lethal E coli challenge in sepsis and septic shock models. In addition to the efficacy of ciVAX against homologous challenge, PAMPS isolated from an infected animal protects other animals against infection by heterologous challenge using different E. coli serotypes - demonstrating the potential for use of ciVAX in controlling pandemics. The advantage of the ciVAX technology is the strong immunogenicity with limited reactogenicity, the use of inactivated pathogens, and the modular manufacture using cGMP approved products which can be stockpiled ready for the next pandemic. One Sentence SummaryBiomaterial vaccine induces strong immunogenicity, weak reactogenicity, and protects from E. coli sepsis in rodents and pigs, and MRSA skin abscess.

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