%0 Journal Article
%T Stat5 opposes the transcription factor Tox and rewires exhausted CD8+ T cells toward durable effector-like states during chronic antigen exposure.
%A Beltra JC
%A Abdel-Hakeem MS
%A Manne S
%A Zhang Z
%A Huang H
%A Kurachi M
%A Su L
%A Picton L
%A Ngiow SF
%A Muroyama Y
%A Casella V
%A Huang YJ
%A Giles JR
%A Mathew D
%A Belman J
%A Klapholz M
%A Decaluwe H
%A Huang AC
%A Berger SL
%A Garcia KC
%A Wherry EJ
%J Immunity
%V 56
%N 12
%D 2023 Dec 12
%M 38091951
%F 43.474
%R 10.1016/j.immuni.2023.11.005
%X 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 (Texprog) to intermediate (Texint) and terminal (Texterm) subsets, suggesting development flexibility. We examined epigenetic transitions between Tex cell subsets and revealed a reciprocally antagonistic circuit between Stat5a and Tox. Stat5 directed Texint cell formation and re-instigated partial effector biology during this Texprog-to-Texint 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:IL2Rβ-pair fostered Texint 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.