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
Publications
Resources
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
For additional information please contact
Brian Kelly
Director, Business Development and Licensing
Phone: (646) 962-7041
Email: bjk44@cornell.edu