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乳腺癌肿瘤微环境中白细胞介素-17 产生细胞浸润是一个不良预后因素。

Interleukin-17-producing cell infiltration in the breast cancer tumour microenvironment is a poor prognostic factor.

机构信息

Department of Pathology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

出版信息

Histopathology. 2013 Aug;63(2):225-33. doi: 10.1111/his.12156. Epub 2013 Jun 6.

Abstract

AIMS

Interleukin-17 (IL-17) is a proinflammatory cytokine that is most prominently produced by T-helper type 17 (Th17) cells, a distinct CD4+ T-helper cell subset. The aim of this study was to investigate the level of IL-17-producing cells in the breast cancer tumour microenvironment and its prognostic role.

METHODS AND RESULTS

A total of 207 breast carcinoma specimens were assessed by IL-17 immunohistochemistry, and the findings were correlated with clinicopathological parameters. We found that increased numbers of IL-17-producing cells were correlated with high histological grade, negative ER/PR status, and triple-negative molecular subtypes segregated by immunoprofiles. However, they did not correlate with stage, tumour size, nodal status, HER2 status, or histological type. Patients with tumours with high numbers of IL-17-producing cells had shorter disease-free survival (DFS) than patients with tumours with low numbers of IL-17-producing cells (P < 0.01). In multivariate analysis, high IL-17 level [hazard ratio (HR) 2.24; 95% CI 1.06-4.75], advanced T stage (HR 2.73; 95% CI 1.30-5.73), positive HER2 status (HR 4.88; 95% CI 1.47-16.18) and triple-negative subtype (HR 7.46; 95% CI 1.38-40.36) were significant prognostic factors for DFS.

CONCLUSIONS

Our results indicate that a high level of IL-17-producing cells in the breast cancer tumour microenvironment is a poor prognostic factor.

摘要

目的

白细胞介素-17(IL-17)是一种促炎细胞因子,主要由辅助性 T 细胞 17(Th17)细胞产生,这是一种独特的 CD4+辅助性 T 细胞亚群。本研究旨在探讨乳腺癌肿瘤微环境中产生 IL-17 的细胞水平及其预后作用。

方法和结果

共对 207 例乳腺癌标本进行 IL-17 免疫组化检测,并将检测结果与临床病理参数相关联。我们发现,产生 IL-17 的细胞数量增加与组织学分级高、ER/PR 状态阴性以及免疫表型分类的三阴性分子亚型相关。然而,它们与分期、肿瘤大小、淋巴结状态、HER2 状态或组织学类型无关。与产生 IL-17 的细胞数量低的肿瘤患者相比,产生 IL-17 的细胞数量高的肿瘤患者无病生存(DFS)时间更短(P < 0.01)。在多变量分析中,高 IL-17 水平[风险比(HR)2.24;95%置信区间 1.06-4.75]、T 期较晚(HR 2.73;95%置信区间 1.30-5.73)、HER2 状态阳性(HR 4.88;95%置信区间 1.47-16.18)和三阴性亚型(HR 7.46;95%置信区间 1.38-40.36)是 DFS 的显著预后因素。

结论

我们的研究结果表明,乳腺癌肿瘤微环境中高水平的产生 IL-17 的细胞是一个不良的预后因素。

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