# Targeting epigenetic regulators to boost T cell immunotherapy against cancer

**Authors:** Tiaojiang Xiao, Ying E. Zhang

PMC · DOI: 10.1186/s13578-026-01533-y · Cell & Bioscience · 2026-02-03

## TL;DR

This paper reviews how epigenetic changes affect T-cell immunotherapy and how targeting these changes could improve cancer treatments.

## Contribution

The paper provides a comprehensive review of epigenetic regulators and their impact on T-cell immunotherapy outcomes.

## Key findings

- Epigenetic regulators influence T-cell differentiation and function.
- Targeting epigenetic pathways can enhance CAR-T and TCR-based therapies.
- Epigenetic changes contribute to T-cell exhaustion and lineage commitment.

## Abstract

Epigenetic regulation is crucial in directing T-cell differentiation, function, and fate, thereby influencing the success of T-cell-based immunotherapies. This review begins with an overview of the evolution of T-cell immunotherapies in cancer treatment. We then examine key epigenetic regulators—such as DNA methylation, mRNA methylation, and histone methylation—and their roles in shaping T-cell states during infection and tumorigenesis. The contributions of these regulators to T-cell exhaustion and lineage commitment are discussed in the context of immunotherapy efficacy. We highlight recent advances in targeting epigenetic pathways to enhance CAR-T and TCR-based therapies and conclude with current challenges and emerging strategies to improve the durability and effectiveness of adoptive T-cell therapies.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}
- **Diseases:** cancer (MESH:D009369), infection (MESH:D007239), tumorigenesis (MESH:D063646)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12958680/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958680/full.md

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Source: https://tomesphere.com/paper/PMC12958680