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| Funder | NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES |
|---|---|
| Recipient Organization | University of California At Davis |
| Country | United States |
| Start Date | Sep 26, 2024 |
| End Date | Aug 31, 2026 |
| Duration | 704 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 11031610 |
PROJECT SUMMARY A successful vaccine for systemic Salmonella infections will need to induce Th1 memory cells, but the tissue location and required functionality of these cells is poorly understood. Our preliminary data show that liver Tissue Resident Memory (TRM) CD4 T cells express higher levels of IL-18R and are more protective than the
corresponding TRMs cells in the lamina propria. In this application, we will test, (i) whether IL-18R expression allows non-cognate responsiveness and robust TRM-mediated protection, and (ii) whether the use of a mRNA nanoparticle delivery system can induce this protective population in the liver of vaccinated mice.
University of California At Davis
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