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Updated: Jun 11, 2025

Measuring Mitochondrial Function of Naïve and Effector CD8 T Cells
Published on: March 28, 2025
Histone lactylation drives CD8+ T cell metabolism and function.
Deblina Raychaudhuri1, Pratishtha Singh1, Bidisha Chakraborty1
1Department of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Histone lactylation, specifically H3K18la and H3K9la, is enriched in CD8+ T cells and regulates their function. Modulating these marks impacts antitumor immunity, revealing their critical role in T cell responses.
Area of Science:
- Immunology
- Epigenetics
- Metabolic pathways
Background:
- CD8+ T cell activation and function are linked to metabolic pathways producing lactate.
- Lactylation, a histone modification from lactate, has unknown relevance in CD8+ T cells.
Purpose of the Study:
- To investigate the role of histone lactylation (H3K18la and H3K9la) in CD8+ T cell activation and function.
- To explore the impact of modulating histone lactylation on CD8+ T cell effector functions and antitumor immunity.
Main Methods:
- Analysis of H3K18la and H3K9la enrichment in human and mouse CD8+ T cells.
- Investigation of distinct lactylation patterns in CD8+ T cell subsets.
- Modulation of lactylation via metabolic and epigenetic targeting in preclinical models.
Main Results:
- H3K18la and H3K9la are enriched in CD8+ T cells and initiate transcription of key functional genes.
- Distinct H3K18la and H3K9la patterns correlate with specific CD8+ T cell metabolic profiles.
- Modulation of H3K18la and H3K9la influences CD8+ T cell effector functions, including antitumor immunity.
Conclusions:
- H3K18la and H3K9la are critical epigenetic marks in CD8+ T cells.
- Histone lactylation plays a significant role in regulating CD8+ T cell function and antitumor immunity.
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