Nutrient-driven histone code determines exhausted CD8+ T cell fates 2309

Abstract Description Exhausted T cells (TEX) in cancer and chronic viral infections undergo metabolic and epigenetic remodeling, impairing their protective capabilities. However, the impact of nutrient metabolism on epigenetic modifications that control TEX differentiation remains unclear. We showed that TEX cells shift from acetate to citrate metabolism by downregulating acetyl-CoA synthetase 2 (ACSS2) while maintaining ATP-citrate lyase (ACLY) activity. This metabolic switch increased citrate-dependent histone acetylation, mediated by histone acetyltransferase KAT2A-ACLY interactions, at TEX signature-genes while reducing acetate-dependent histone acetylation, dependent on p300-ACSS2 complexes, at effector and memory T cell genes. Nuclear ACSS2 overexpression or ACLY inhibition prevented TEX differentiation and enhanced tumor-specific T cell responses. These findings unveiled a nutrient-instructed histone code governing CD8+ T cell differentiation, with implications for metabolic- and epigenetic-based T cell therapies. Funding Sources R01 AI066232 ; R21 AI151986 ; Cancer Research Institute fellowship Topic Categories Immune Response Regulation: Molecular Mechanisms (IRM)

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Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.240
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Nutrient-driven histone code determines exhausted CD8+ T cell fates 2309

Russell G. Jones, Thomas H. Mann, Michael S. Dahabieh, Susan M. Kaech et al.
The Journal of Immunology
Immune cells in cancer
article

Nutrient-driven histone code determines exhausted CD8+ T cell fates 2309

Russell G. Jones, Thomas H. Mann, Michael S. Dahabieh, Susan M. Kaech, Shixin Ma
article en

Abstract

Abstract Description Exhausted T cells (TEX) in cancer and chronic viral infections undergo metabolic and epigenetic remodeling, impairing their protective capabilities. However, the impact of nutrient metabolism on epigenetic modifications that control TEX differentiation remains unclear. We showed that TEX cells shift from acetate to citrate metabolism by downregulating acetyl-CoA synthetase 2 (ACSS2) while maintaining ATP-citrate lyase (ACLY) activity. This metabolic switch increased citrate-dependent histone acetylation, mediated by histone acetyltransferase KAT2A-ACLY interactions, at TEX signature-genes while reducing acetate-dependent histone acetylation, dependent on p300-ACSS2 complexes, at effector and memory T cell genes. Nuclear ACSS2 overexpression or ACLY inhibition prevented TEX differentiation and enhanced tumor-specific T cell responses. These findings unveiled a nutrient-instructed histone code governing CD8+ T cell differentiation, with implications for metabolic- and epigenetic-based T cell therapies. Funding Sources R01 AI066232 ; R21 AI151986 ; Cancer Research Institute fellowship Topic Categories Immune Response Regulation: Molecular Mechanisms (IRM)

The Journal of ImmunologyVol. 214(Supplement_1)
Salk Institute for Biological Studies (US)
National Institutes of Health
Openalex Percentile: Top 61%
Immune cells in cancer
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