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| |  Most vaccines are delivered by injection, which increases the risk that HIV, hepatitis, and other serious diseases may be transmitted by syringes and needles that are not sterile. In the developing world, infections in the respiratory and intestinal tracts are major causes of sickness and death, especially among children. Vaccine delivery systems that can target respiratory or intestinal mucosal tissue and stimulate immune response there have the potential to be particularly effective against these infections.
Dr. Lo's project addresses two needs: the development of vaccine delivery systems that do not require needles and the design of systems that target specific tissues in the body. Using influenza vaccination as a model, Dr. Lo and his team are working to bind vaccine to specially designed molecules that target mucosal tissue. While their study uses influenza vaccine as a focus, investigators expect the technology potentially could be applied to any pathogen that causes disease in mucosal tissue. They envision vaccines will be given either orally or as nasal spray.
Investigators are producing their first vaccine formulations with fusion proteins that contain influenza hemagglutinin and a targeting peptide, and are in the process of testing the fusion proteins for their ability to enhance immune response in mice. |
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| | | Developing short peptide ligands for receptors on specialized intestinal epithelial cells (M cells) known to be involved in presentation of antigens to the mucosal immune system | | | | | Developing formulation technologies that allow rapid, large-scale production of new antigen-ligand recombinant protein vaccines | | | | | Evaluating the potency of vaccine formulations in a preclinical mouse model | | |
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| | | The project team has demonstrated that two peptides can bind to their target M cell receptor, Claudin 4. Investigators established proof of principle by showing that, compared with controls, fluorescent beads coated with peptides targeting Claudin 4 can mediate selective uptake in the Peyer’s patches of the small intestines of mice. | | |
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| | | University of California, Riverside , University of California, Riverside, California, United States - US | | |
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