Method of use for benzofuran compounds
AssigneeTampa Bay Research Institute
InventorsWilliam Bradley, Amara Davis, Claire O'Connor, Jessica Mandula, Nicole Perekhodko, Akiko Tanaka
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AssigneeTampa Bay Research Institute
InventorsWilliam Bradley, Amara Davis, Claire O'Connor, Jessica Mandula, Nicole Perekhodko, Akiko Tanaka
Estimating the term…
An orally bioavailable benzofuran is provided which possesses in vitro and in vivo capabilities able to overcome issues in loading of antigenic peptide on major histocompatibility class I complexes, including on the surface of professional antigen presenting cells. The design of immunotherapies such as dendritic cell vaccines, optimal binding of the antigenic peptides to MHC class I complexes is a major challenge. Current therapeutic peptide loading is expensive, labor-intensive, or requires in vitro manipulation. Models demonstrate that the benzofuran enhances T-cell activation through increased peptide binding to cell surface MHC class I complexes. Molecular docking studies indicate the benzofuran binds the F pocket of MHC class I in a similar manner to high-affinity peptides and TAPBPR, aiding in the targeted loading of exogenous peptides. The therapeutic potential was demonstrated when using PLGA particles of BzFβ were injected intramuscularly, and significantly inhibited the development of E.G7-OVA tumors.
A method of modulating an immune response, comprising:
A method of enhancing a vaccine, comprising:
A method of preparing an immunotherapy, comprising:
A method of preparing an in vivo immunotherapy, comprising:
Dependencies are inferred from the claim text.