Abstract 7398: Senescent regulatory T cells retain potent suppressive function in clear cell renal cell carcinoma

Abstract Clear cell renal cell carcinoma (ccRCC) is an aging-associated malignancy characterized by a highly immunosuppressive, immune-rich tumor microenvironment and variable response to immune checkpoint blockade. Regulatory T cells (Tregs) are dominant orchestrators of immune suppression in ccRCC, yet the functional consequences of cellular senescence in these cells remain unknown and are widely presumed to be impairing. Single-cell RNA sequencing of treatment-naïve human ccRCC tumors revealed a distinct tumor-infiltrating Treg (TI-Treg) subpopulation co-expressing classic senescence markers (p16^INK4a, p21), senescence-associated β-galactosidase activity (SA-β-gal), BCL-xL, and robust immunosuppressive effector programs. Contrary to the prevailing view that senescence attenuates Treg function, we hypothesized that senescent TI-Tregs retain potent suppressive capacity. To functionally characterize these senescent TI-Treg subsets, we used a novel activity-based fluorescent senescence probe that labels SA-β-gal and employed p16-tdTomato reporter mice for the isolation of viable senescent TI-Tregs. Additionally, using an in vitro co-culture system in which naïve Tregs are driven into senescence by ccRCC cell-derived factors, suppression assays demonstrated that senescent Tregs maintain strong inhibitory activity against CD4+ T-cell proliferation, comparable to non-senescent Tregs. Concomitant RNA sequencing confirmed persistence of canonical immunosuppressive pathways and acquisition of a senescence-reinforced suppressive transcriptome. These findings challenge the assumptions that senescence Tregs are dysfunctional in cancer and establish senescent Tregs as critical contributors to immunosuppression in aging-associated ccRCC. This work unravels senescent TI-Tregs as therapeutic targets/vulnerabilities for their selective elimination to restore antitumor immunity. Citation Format: Temitope Mary Ogunmola, Myung-Chul Kim, Zeng Jin, Umasankar de, Lina Cui, Guangrong Zheng, Ryan Kolb, Weizhou Zhang. Senescent regulatory T cells retain potent suppressive function in clear cell renal cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7398.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7398
Primary Topic
Telomeres, Telomerase, and Senescence
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article
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article

Abstract 7398: Senescent regulatory T cells retain potent suppressive function in clear cell renal cell carcinoma

Zeng Jin, Myung‐Chul Kim, Ryan Kolb, Weizhou Zhang et al.
Cancer Research
Telomeres, Telomerase, and Senescence
article

Abstract 7398: Senescent regulatory T cells retain potent suppressive function in clear cell renal cell carcinoma

Zeng Jin, Myung‐Chul Kim, Ryan Kolb, Weizhou Zhang, Umasankar De, Temitope Ogunmola, Lina Cui, Guangrong Zheng
article en

Abstract

Abstract Clear cell renal cell carcinoma (ccRCC) is an aging-associated malignancy characterized by a highly immunosuppressive, immune-rich tumor microenvironment and variable response to immune checkpoint blockade. Regulatory T cells (Tregs) are dominant orchestrators of immune suppression in ccRCC, yet the functional consequences of cellular senescence in these cells remain unknown and are widely presumed to be impairing. Single-cell RNA sequencing of treatment-naïve human ccRCC tumors revealed a distinct tumor-infiltrating Treg (TI-Treg) subpopulation co-expressing classic senescence markers (p16^INK4a, p21), senescence-associated β-galactosidase activity (SA-β-gal), BCL-xL, and robust immunosuppressive effector programs. Contrary to the prevailing view that senescence attenuates Treg function, we hypothesized that senescent TI-Tregs retain potent suppressive capacity. To functionally characterize these senescent TI-Treg subsets, we used a novel activity-based fluorescent senescence probe that labels SA-β-gal and employed p16-tdTomato reporter mice for the isolation of viable senescent TI-Tregs. Additionally, using an in vitro co-culture system in which naïve Tregs are driven into senescence by ccRCC cell-derived factors, suppression assays demonstrated that senescent Tregs maintain strong inhibitory activity against CD4+ T-cell proliferation, comparable to non-senescent Tregs. Concomitant RNA sequencing confirmed persistence of canonical immunosuppressive pathways and acquisition of a senescence-reinforced suppressive transcriptome. These findings challenge the assumptions that senescence Tregs are dysfunctional in cancer and establish senescent Tregs as critical contributors to immunosuppression in aging-associated ccRCC. This work unravels senescent TI-Tregs as therapeutic targets/vulnerabilities for their selective elimination to restore antitumor immunity. Citation Format: Temitope Mary Ogunmola, Myung-Chul Kim, Zeng Jin, Umasankar de, Lina Cui, Guangrong Zheng, Ryan Kolb, Weizhou Zhang. Senescent regulatory T cells retain potent suppressive function in clear cell renal cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7398.

Cancer ResearchVol. 86(7_Supplement)
Kyungpook National University (KR), University of Florida (US), Sungkyunkwan University (KR), Florida College (US)
Good health and well-being
Openalex Percentile: Top 24%
Telomeres, Telomerase, and Senescence
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