T-FINDER: A highly sensitive, pan-HLA platform for functional T cell receptor and ligand discovery.
Miray CetinVeronica PinamontiTheresa SchmidTamara BoschertAna Mellado FuentesKristina KromerTaga LernerJing ZhangYonatan HerzigChristopher EhlertMiguel Hernandez-HernandezGeorgios SamarasClaudia Maldonado TorresLaura I FischValeriia DraganArlette KouwenhovenBertrand Van SchoubroeckHans WilsCarl Van HoveMichael PlattenEdward W GreenFrederik StevenaertNathan J FelixJohn M LindnerPublished in: Science advances (2024)
Effective, unbiased, high-throughput methods to functionally identify both class II and class I HLA-presented T cell epitopes and their cognate T cell receptors (TCRs) are essential for and prerequisite to diagnostic and therapeutic applications, yet remain underdeveloped. Here, we present T-FINDER [T cell Functional Identification and (Neo)-antigen Discovery of Epitopes and Receptors], a system to rapidly deconvolute CD4 and CD8 TCRs and targets physiologically processed and presented by an individual's unmanipulated, complete human leukocyte antigen (HLA) haplotype. Combining a highly sensitive TCR signaling reporter with an antigen processing system to overcome previously undescribed limitations to target expression, T-FINDER both robustly identifies unknown peptide:HLA ligands from antigen libraries and rapidly screens and functionally validates the specificity of large TCR libraries against known or predicted targets. To demonstrate its capabilities, we apply the platform to multiple TCR-based applications, including diffuse midline glioma, celiac disease, and rheumatoid arthritis, providing unique biological insights and showcasing T-FINDER's potency and versatility.
Keyphrases
- high throughput
- rheumatoid arthritis
- regulatory t cells
- celiac disease
- small molecule
- single cell
- genome wide
- endothelial cells
- crispr cas
- living cells
- disease activity
- binding protein
- low grade
- oxidative stress
- dna methylation
- high resolution
- fluorescent probe
- ankylosing spondylitis
- systemic lupus erythematosus
- dendritic cells
- peripheral blood
- nk cells
- label free
- mass spectrometry