
IL-2は、慢性感染においてCD8+ T細胞の効果機能を増強するが、CXCR5+ TPEX細胞の分化を抑制し、B細胞濾胞への局在を阻害する。


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Cytotoxic CD8+ T cells, essential in combating viral infections and cancer, become dysfunctional from prolonged antigen exposure. Precursors of exhausted T (TPEX) cells are pivotal in sustaining immune responses in chronic diseases and mediating immunotherapy efficacy. They also control viral infection within B-cell follicles, facilitated by CXCR5 expression. How cytokines regulate TPEX cell fate and follicular entry is not well understood. We reveal that IL-2 treatment enhances CD8+ T cell effector functions in chronic LCMV infection but hinders CXCR5+ TPEX cell formation and infection control within B-cell follicles. Mechanistically, IL-2 suppresses TPEX cell differentiation in a STAT5 and BLIMP1-dependent manner. Using an IL-2 fusion protein targeting CD122, we shifted the differentiation towards CX3CR1+ T cells with increased effector function. Clinical observations with low-dose IL-2 in autoimmune disease confirmed IL-2’s inhibitory effect on CXCR5+ TPEX cells, underscoring IL-2’s crucial regulatory role and therapeutic potential in modulating TPEX and effector T cell generation.

### Competing Interest Statement

The authors have declared no competing interest.

IL-2 enhances effector function but suppresses follicular localization of CD8+ T cells in chronic infection

慢性感染におけるcd8-t細胞の機能と濾胞局在性を調整するil-2の役割


慢性感染におけるCD8+ T細胞の機能と濾胞局在性を調整するIL-2の役割
