The effector program of human CD8 T cells supports tissue remodeling.
Michael DelacherLisa SchmidleithnerMalte SimonPhilipp StüveLieke SanderinkAgnes Hotz-WagenblattMarina WuttkeKathrin SchambeckBrigitte RuhlandVeronika HofmannSebastian BittnerUwe RitterAsmita PantSara Salome HelbichMorten VossNiels A W LemmermannLisa Bessiri-SchakeToszka BohnAndreas EigenbergerAyse Nur MenevseClaudia GebhardNicholas StriederHinrich AbkenMichael RehliJochen HuehnPhilipp BeckhoveThomas HehlgansHenrik JungerEdward K GeisslerLukas PrantlJens M WernerChristian SchmidlBenedikt BrorsCharles D ImbuschMarkus FeuererPublished in: The Journal of experimental medicine (2024)
CD8 T lymphocytes are classically viewed as cytotoxic T cells. Whether human CD8 T cells can, in parallel, induce a tissue regeneration program is poorly understood. Here, antigen-specific assay systems revealed that human CD8 T cells not only mediated cytotoxicity but also promoted tissue remodeling. Activated CD8 T cells could produce the epidermal growth factor receptor (EGFR)-ligand amphiregulin (AREG) and sensitize epithelial cells for enhanced regeneration potential. Blocking the EGFR or the effector cytokines IFN-γ and TNF could inhibit tissue remodeling. This regenerative program enhanced tumor spheroid and stem cell-mediated organoid growth. Using single-cell gene expression analysis, we identified an AREG+, tissue-resident CD8 T cell population in skin and adipose tissue from patients undergoing abdominal wall or abdominoplasty surgery. These tissue-resident CD8 T cells showed a strong TCR clonal relation to blood PD1+TIGIT+ CD8 T cells with tissue remodeling abilities. These findings may help to understand the complex CD8 biology in tumors and could become relevant for the design of therapeutic T cell products.
Keyphrases
- stem cells
- epidermal growth factor receptor
- endothelial cells
- adipose tissue
- small cell lung cancer
- quality improvement
- patients undergoing
- single cell
- tyrosine kinase
- immune response
- high throughput
- metabolic syndrome
- induced pluripotent stem cells
- acute coronary syndrome
- genome wide
- risk assessment
- gene expression
- climate change
- pluripotent stem cells
- wound healing
- anti inflammatory
- nk cells