4.7 Article

Distribution of Th17 cells and Foxp3-expressing T cells in tumor-infiltrating lymphocytes in patients with uterine cervical cancer

Journal

CLINICA CHIMICA ACTA
Volume 413, Issue 23-24, Pages 1848-1854

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cca.2012.07.012

Keywords

Uterine cervical cancer; Cervical intraepithelial neoplasia; Th17 cells; Foxp3-expressing T cells

Funding

  1. National Natural Science Foundation of China [81072122, 81172486, 81170515]

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Background: Recent studies suggest a potential impact of Th17 cells on tumor. In the present study, we investigated the distribution of Th17 cells in relation to Foxp3-expressing T cells in the tumor-infiltrating lymphocytes (Ills) from patients with uterine cervical cancer (UCC), cervical tissues from patients with cervical intraepithelial neoplasia (ON) and healthy cervical tissues. Methods: Th17 cells and Foxp3-expressing T cells were evaluated by immunohistochemical staining. IL-6, TGF-beta, IL-17 and IL-10 were detected by enzyme-linked immunosorbent assay (ELISA). Immunohistochemical staining for microvessel density (MVD) was performed in order to assess the association of IL-17 expression with angiogenesis. Results: Compared with controls, patients with UCC or CIN had a higher proportion of Th17 cells and Foxp3-expressing T cells, when the ratio of Th17/Foxp3-expressing T cells in TILs was decreased in individual cases, it was more markedly decreased in TILs than normal cervical tissues. Meanwhile, the cytokine(IL-6, TGF-beta and IL-10) concentrations were significantly higher in UCC patients than those in healthy controls. Interestingly, the levels of intratumoral Th17 cells were positively correlated with MVD in tumors. Conclusions: The imbalance of Th17/Foxp3-expressing T cells may play critical roles in the development and progression of UCC and Th17 cells may promote tumor progression by fostering angiogenesis. (C) 2012 Elsevier B.V. All rights reserved.

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