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Harnessing Metabolic Modulation of Tregs and Dendritic Cells to Enhance Immunotherapy Efficacy (18)

Subject Area Immunology
Term since 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 318346496
 
Cancer immune evasion limits ICB therapy, with Treg expansion contributing to resistance and tumor growth. Tregs also suppress immunity in chronic infections like tuberculosis. We discovered a bacterial peptide which inhibits Treg differentiation, reduces tumor burden in mice, and shows potential for cancer and infection therapy. Its molecular mechanism is independent of Foxm1, possibly acting via proteasomal or mitochondrial pathways. Combining this compound with Batf3-DC recruitment strategies may enhance ICB efficacy. Future work aims to optimize derivatives for safety and solubility.
DFG Programme Collaborative Research Centres
 
 

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