Functions of human liver CD69(+)CD103(-)CD8(+) T cells depend on HIF-2 alpha activity in healthy and pathologic livers

Abstract

Background & Aims: Human liver CD69(+)CD8(+) T cells are similar to 95% CD103(-) and similar to 5% CD103(+). Although CD69(+)CD103(+)CD8(+) T cells show tissue residency and robustly respond to antigens, CD69(+)CD103(-)CD8(+) T cells are not yet well understood. Methods: Liver perfusate and paired peripheral blood were collected from healthy living donors and recipients with cirrhosis during liver transplantation. Liver tissues were obtained from patients with acute hepatitis A. Phenotypic and functional analyses were performed by flow cytometry. Gene expression profiles were determined by microarray and quantitative reverse transcription PCR. PT-2385 was used to inhibit hypoxia-inducible factor (HIF)-2 alpha. Results: Human liver CD69(+)CD103(-)CD8(+) T cells exhibited HIF-2 alpha upregulation with a phenotype of tissue residency and terminal differentiation. CD103(-) cells comprised non-hepatotropic virus-specific T cells as well as hepatotropic virus-specific T cells, but CD103(+) cells exhibited only hepatotropic virus specificity. Although CD103(-) cells were weaker effectors on a per cell basis than CD103(+) cells, following T cell receptor or interleukin-15 stimulation, they remained the major CD69(+)CD8(+) effector population in the liver, surviving with less cell death. An HIF-2 alpha inhibitor suppressed the effector functions and survival of CD69(+)CD103(-)CD8(+) T cells. In addition, HIF-2a alpha expression in liver CD69(+)CD103(-)CD8(+) T cells was significantly increased in patients with acute hepatitis A or cirrhosis. Conclusions: Liver CD69(+)CD103(-)CD8(+) T cells are tissue resident and terminally differentiated, and their effector functions depend on HIF-2 alpha. Furthermore, activation of liver CD69(+)CD103(-)CD8(+) T cells with HIF-2 alpha upregulation is observed during liver pathology. Lay summary: The immunologic characteristics and the role of CD69(+)CD103(-)CD8(+) T cells, which are a major population of human liver CD8(+) T cells, remain unknown. Our study shows that these T cells have a terminally differentiated tissue-resident phenotype, and their effector functions depend on a transcription factor, HIF-2 alpha. Furthermore, these T cells were activated and expressed higher levels of HIF-2 alpha in liver pathologies, suggesting that they play an important role in immune responses in liver tissues and the pathogenesis of human liver disease.