Bacterial RNAs As Vaccine Adjuvants

Principal Investigator: 

Julie Magarian Blander, Gladys and Roland Harriman Professor of Immunology in Medicine

Background & Unmet Need

  • Vaccines containing live, attenuated pathogens trigger stronger and longer-lasting immune responses compared to those containing killed pathogens
  • Live vaccines carry potential risks to immuno-compromised individuals, as well as a more expensive and complex supply chain
  • Adjuvants are compounds which increase local and systemic immune reactions to vaccines
  • Current adjuvants (aluminum, oils, or salts) do not elicit the same immune response as live pathogens
  • Canonical molecular patterns that alert the immune system of pathogens are present in both live and killed vaccines, suggesting an uncharacterized signal of pathogen viability to our immune system
  • Unmet Need: Development of a non-live vaccine which elicits a robust immune response comparable to that of live vaccines

Technology Overview

  • The Technology: Bacterial mRNAs as adjuvants to induce robust immune response in both prophylactic and therapeutic vaccines
  • The Discovery: The inventors showed that RNA is destroyed when a pathogen is heat-killed prior to injection, and that heat-killed bacteria alone elicit poor immune response
  • Addition of purified bacterial RNA to heat-killed E. coli (HKEC) vaccines induced strong cytokine production and increases adaptive immune response
  • PoC Data: Compared to HKEC alone, HKEC + RNA induced higher levels of IL-1β and IFN-β in dendritic cells
  • HKEC + RNA stimulated an increase of class-switched IgG antibody titers in mice (p ≤ 0.01)
  • HKEC + RNA improved both primary and memory T cell responses, as well as increased death of infected cells

Technology Applications

  • Improved vaccine potency for humans, pets, and livestock
  • Use as adjuvant for vaccines against infectious disease, cancer prevention, and cancer immunotherapies
  • Can be used in live, antigen, or mRNA vaccines

Technology Advantages

  • Stronger and longer-lasting immune response compared to traditional killed vaccines, without the safety risk and supply chain considerations of live vaccines
  • Synthetic bacterial RNAs also elevate immune response, suggesting potential for design of even more effective RNA adjuvants

Figure: dendritic cell IL-1β and IFN-β levels in response to E. coli (EC), heat-killed E. coli(HKEC), or HKEC + bacterial RNA.

Intellectual Property

Patents

  • US Patent 9,844,592. "Bacterial RNAs as vaccine adjuvants." Issued Dec 19, 2017.
  • US Patent 10.588,964. "Bacterial RNAs as vaccine adjuvants." Issued Mar 17, 2020.

Cornell Reference

  • 8328

Contact Information

Brian Kelly, Ph.D.

For additional information please contact

Brian Kelly
Director, Business Development and Licensing
Phone: (646) 962-7041
Email: bjk44@cornell.edu