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.
Authors
- Zeng Jin
- Myung‐Chul Kim (ORCID: https://orcid.org/0000-0003-3389-1244)
- Ryan Kolb (ORCID: https://orcid.org/0000-0001-6305-2885)
- Weizhou Zhang (ORCID: https://orcid.org/0000-0002-8236-0346)
- Umasankar De (ORCID: https://orcid.org/0000-0003-4478-791X)
- Temitope Ogunmola
- Lina Cui
- Guangrong Zheng
Institutions
- Kyungpook National University (KR)
- University of Florida (US)
- Sungkyunkwan University (KR)
- Florida College (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2026-04-03
- DOI
- https://doi.org/10.1158/1538-7445.am2026-7398
- Primary Topic
- Telomeres, Telomerase, and Senescence
- Type
- article
- Field-Weighted Citation Impact
- 0.00