All-trans retinoic acid suppresses CD8+ T-cell terminal exhaustion and potentiates anti-PD-1 therapy in glioblastoma
Terminal exhaustion of CD8⁺ T cells limits the efficacy of immune checkpoint blockade (ICB), particularly in glioblastoma, which is characterized by an immunosuppressive tumor microenvironment. Therefore, a better understanding of the regulators of terminal exhaustion could overcome intrinsic resistance to ICB and improve the efficacy of immunotherapy. In this study, we report that all-trans retinoic acid (ATRA) suppresses CD8⁺ T-cell terminal exhaustion. The administration of ATRA during CD8⁺ T-cell activation in vitro conferred resistance to terminal exhaustion and preserved effector cytokine production and effector function. Mechanistically, ATRA selectively induced the expression of the long isoform of T-cell factor 1 (TCF-1 βBD ) through activation of the canonical WNT/β-catenin pathway. In a mouse glioma model, adoptively transferred ATRA-conditioned CD8⁺ T cells exhibited increased TCF-1 βBD and β-catenin expression and resistance to exhaustion, which led to superior tumor-infiltrating CD8 + T-cell polyfunctionality and enhanced glioma suppression. Importantly, oral administration of ATRA also suppressed terminal exhaustion of tumor-infiltrating CD8 + T cells and synergized with anti-PD-1 therapy, overcoming resistance to immune checkpoint blockade (ICB) in two mouse models of glioma. Combined ATRA and anti-PD-1 treatment also displayed synergistic therapeutic potential by significantly reducing recurrence in a mouse model of glioma that had undergone surgical resection. Single-cell transcriptomic analysis of glioblastoma patients receiving anti-PD-1 therapy revealed that CD8⁺ T cells from responders were enriched in genes that respond to retinoic acid and WNT-associated genes, which correlated with improved survival. These findings establish ATRA as a modulator of CD8⁺ T-cell exhaustion through the induction of WNT/β-catenin-dependent TCF-1 βBD expression, suggesting that ATRA has therapeutic potential for overcoming resistance to ICB in glioma.
Authors
- Byeong Hoon Kang
- Heung Kyu Lee (ORCID: https://orcid.org/0000-0002-3977-1510)
- Jeongwoo La (ORCID: https://orcid.org/0000-0002-8153-7402)
- Stephen Ahn (ORCID: https://orcid.org/0000-0002-6854-1597)
- Hyeon Cheol Kim (ORCID: https://orcid.org/0000-0003-3370-8438)
- Chae Won Kim (ORCID: https://orcid.org/0009-0009-2643-4855)
- Sung Ki Lee (ORCID: https://orcid.org/0000-0002-6941-192X)
- Minji Kim (ORCID: https://orcid.org/0009-0008-7807-7389)
- Hyunjin Kim
- Yumin Kim
- IN KANG
- Hyeoncheol Kim
- Inju Hwang
- WonHyung Park
- 김민지
- Seo Hyeon Im (ORCID: https://orcid.org/0009-0009-9146-5615)
- Won Hyung Park
- Jae-Byum Chang
Institutions
- Korea Advanced Institute of Science and Technology (KR)
- Konyang University (KR)
- Regenerative Medicine Institute (MX)
- The Catholic University of Korea Seoul St. Mary's Hospital (KR)
- Catholic University of Korea (KR)
Publication Details
- Journal
- Signal Transduction and Targeted Therapy
- Published
- 2026-08-26
- DOI
- https://doi.org/10.1038/s41392-026-02852-9
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Research Foundation
- Korea Health Industry Development Institute
- National Research Foundation of Korea
- Samsung Science and Technology Foundation
- Samsung