Prognostic value of regulatory T cells and T helper 17 cells in high grade serous ovarian carcinoma

J Cancer Res Clin Oncol. 2023 Jun;149(6):2523-2536. doi: 10.1007/s00432-022-04101-2. Epub 2022 Jun 28.

Abstract

Purpose: In recent years the tumor microenvironment and its interaction with the tumor has emerged into research focus with increased attention to the composition of Tumor-infiltrating lymphocytes. We wanted to quantify the composition of Regulatory T cells (Tregs) and T helper 17 cells (Th17 cells) and their prognostic impact in high-grade serous tubo-ovarian carcinoma.

Methods: Tregs and Th17 cells were determined by immunohistochemical analysis of CD25 FoxP3 and RORγt, respectively on tissue microarrays of a cohort of 222 patients with reviewed histology and available clinical data. Expression was analyzed with Qupath for quantification and integration with clinical data enabled calculation of prognostic impact. For validation FOXP3 and RORC mRNA expression levels from 502 patients with HGSC in publicly available datasets were evaluated.

Results: An average percentage of 0.93 Tregs and of 0.06 Th17 cells was detected per cells in overall tissue. Optimal cut-offs were determined and higher Tregs were associated with a better overall survival in stroma (p = 0.006), tumor area (p = 0.0012) and overall tissue (p = 0.02). After accounting for well-known prognostic factors age at diagnosis, residual tumor and FIGO stage, this association remained significant for stromal Tregs with overall survival (p = 0.02). Survival analysis for Th17 cells revealed no significant association with survival rates. Moreover, lower Th17/Treg ratios had a positive impact on patient overall survival (p = 0.025 tumor, p = 0.049 stroma and p = 0.016 overall tissue).

Conclusion: Our results outline a positive prognostic effect for higher Tregs but not for Th17 in high grade serous tubo-ovarian carcinoma.

Keywords: Digital pathology; High grade ovarian carcinoma; Prognosis; Regulatory T-cells; Tumor microenvironment; Tumor-infiltrating lymphocytes.

MeSH terms

  • Female
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Lymphocytes, Tumor-Infiltrating / pathology
  • Ovarian Neoplasms* / pathology
  • Prognosis
  • T-Lymphocytes, Regulatory* / pathology
  • Th17 Cells / metabolism
  • Th17 Cells / pathology
  • Tumor Microenvironment

Substances

  • Forkhead Transcription Factors