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The role of short expressed peptides and cell type composition in autoimmune liver inflamma-tion (A06)

Subject Area Gastroenterology
Term since 2025
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 530990199
 
To gain new insights into the pathogenesis of autoimmune liver diseases, we will study human hepatic translational events by measuring genome-wide active translation with ribosome profiling (Ribo-seq). This will allow us to identify novel short open reading frames-encoded peptides in RNA regions previously classified as non-coding. By comparing patients and controls, we will detect disease specific expression of annotated and novel peptides, potentially discovering new self-antigens and pep-tides related to triggering autoimmune B and T cell responses that lead to the break of selftolerance, and/or modulation of inflammation and fibrosis. Moreover, by building a single cell atlas we will discern fundamental causes of maladaptive hepatic immune regulation and infer new strategies to limit them.
DFG Programme Collaborative Research Centres
Applicant Institution Universität Hamburg
 
 

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