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乳腺癌中 Foxp3 调节性 T 细胞浸润的区域性差异及其预后意义。

Zonal difference and prognostic significance of foxp3 regulatory T cell infiltration in breast cancer.

机构信息

Department of Pathology, Ewha Womans University School of Medicine, Seoul, Korea.

Department of Surgery, Ewha Womans University School of Medicine, Seoul, Korea.

出版信息

J Breast Cancer. 2014 Mar;17(1):8-17. doi: 10.4048/jbc.2014.17.1.8. Epub 2014 Mar 28.

Abstract

PURPOSE

Forkhead box P3 (Foxp3) is known as the most specific marker for regulatory T lymphocytes, which play an important role in immune tolerance to disturb antitumor immunity. The present study aimed to investigate the prognostic significance of Foxp3 regulatory T lymphocyte (Foxp3 Treg) infiltration in breast cancer.

METHODS

Immunohistochemical studies with Foxp3, CD4, and CD8 were performed on representative full tissue sections from 143 patients with invasive ductal carcinoma, not otherwise specified. Foxp3 Treg infiltration and the ratios between Foxp3 Treg and CD4 or CD8 T cells were separately analyzed for the tumor bed and tumor periphery to evaluate their association with different clinicopathological parameters and patients' outcome.

RESULTS

The tumor periphery was considerably more densely infiltrated by Foxp3 Treg, CD4, and CD8 T cells than the tumor bed. Unfavorable clinicopathological parameters (a Ki-67 labeling index of ≥14%, a worse histologic grade, a worse nuclear grade, hormone receptor negativity, human epidermal growth factor receptor 2 positivity, and tumor recurrence) were associated with increased Foxp3 Treg infiltration and a high ratio between Foxp3 Treg and CD4/CD8 T cells. In the tumor periphery, as Foxp3 Treg infiltration and the Foxp3 Treg/CD8 ratio increased, patients' 5-year disease-free survival rate decreased.

CONCLUSION

The infiltration densities of Foxp3 Treg, CD4, and CD8 T cells were markedly different between the tumor bed and periphery. Besides the absolute count of Foxp3 Treg, the ratio between Foxp3 Treg and effector T cells was a significant prognostic factor in breast cancer.

摘要

目的

叉头框蛋白 P3(Foxp3)被认为是调节性 T 淋巴细胞(Treg)最特异的标志物,其在免疫耐受中发挥重要作用,以干扰抗肿瘤免疫。本研究旨在探讨 Foxp3 调节性 T 淋巴细胞(Foxp3 Treg)浸润在乳腺癌中的预后意义。

方法

对 143 例非特殊型浸润性导管癌患者的代表性全组织切片进行 Foxp3、CD4 和 CD8 的免疫组织化学研究。分别分析肿瘤床和肿瘤周边 Foxp3 Treg 浸润及 Foxp3 Treg 与 CD4 或 CD8 T 细胞的比例,以评估其与不同临床病理参数和患者预后的关系。

结果

肿瘤周边的 Foxp3 Treg、CD4 和 CD8 T 细胞浸润密度明显高于肿瘤床。不良的临床病理参数(Ki-67 标记指数≥14%、组织学分级较差、核分级较差、激素受体阴性、人表皮生长因子受体 2 阳性、肿瘤复发)与 Foxp3 Treg 浸润增加和 Foxp3 Treg/CD4/CD8 比值升高相关。在肿瘤周边,随着 Foxp3 Treg 浸润和 Foxp3 Treg/CD8 比值的增加,患者的 5 年无病生存率下降。

结论

Foxp3 Treg、CD4 和 CD8 T 细胞在肿瘤床和周边的浸润密度有显著差异。除了 Foxp3 Treg 的绝对计数外,Foxp3 Treg 与效应 T 细胞的比值是乳腺癌的一个重要预后因素。

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