| First Author | Beltra JC | Year | 2023 |
| Journal | Immunity | Volume | 56 |
| Issue | 12 | Pages | 2699-2718.e11 |
| PubMed ID | 38091951 | Mgi Jnum | J:348710 |
| Mgi Id | MGI:7568719 | Doi | 10.1016/j.immuni.2023.11.005 |
| Citation | Beltra JC, et al. (2023) Stat5 opposes the transcription factor Tox and rewires exhausted CD8(+) T cells toward durable effector-like states during chronic antigen exposure. Immunity 56(12):2699-2718.e11 |
| abstractText | Rewiring exhausted CD8(+) T (Tex) cells toward functional states remains a therapeutic challenge. Tex cells are epigenetically programmed by the transcription factor Tox. However, epigenetic remodeling occurs as Tex cells transition from progenitor (Tex(prog)) to intermediate (Tex(int)) and terminal (Tex(term)) subsets, suggesting development flexibility. We examined epigenetic transitions between Tex cell subsets and revealed a reciprocally antagonistic circuit between Stat5a and Tox. Stat5 directed Tex(int) cell formation and re-instigated partial effector biology during this Tex(prog)-to-Tex(int) cell transition. Constitutive Stat5a activity antagonized Tox and rewired CD8(+) T cells from exhaustion to a durable effector and/or natural killer (NK)-like state with superior anti-tumor potential. Temporal induction of Stat5 activity in Tex cells using an orthogonal IL-2:IL2Rbeta-pair fostered Tex(int) cell accumulation, particularly upon PD-L1 blockade. Re-engaging Stat5 also partially reprogrammed the epigenetic landscape of exhaustion and restored polyfunctionality. These data highlight therapeutic opportunities of manipulating the IL-2-Stat5 axis to rewire Tex cells toward more durably protective states. |
