Department of Urology, Nara Medical University, 840 Shijo-cho, Kashihara-shi, Nara 634-8522, Japan.
Department of Pathology, Nara Medical University, 840 Shijo-cho, Kashihara-shi, Nara 634-8522, Japan.
Int J Mol Sci. 2017 Oct 19;18(10):2186. doi: 10.3390/ijms18102186.
The clinical significance of regulatory T cells (Treg) and tumor-associated macrophages (TAM) in the tumor microenvironment of human bladder cancer remains unclear. The aim of this study is to explore their relevance to oncological features in non-muscle invasive bladder cancer (NMIBC). We carried out immunohistochemical analysis of forkhead box P3 (FOXP3, Treg maker), CD204 (TAM marker), and interleukin-6 (IL6) using surgical specimens obtained from 154 NMIBC patients. The Treg and TAM counts surrounding the cancer lesion and IL6-positive cancer cell counts were evaluated against clinicopathological variables. We focused on the ability of the Treg and TAM counts around the cancer lesion to predict outcomes after adjuvant intravesical Bacille Calmette-Guérin (BCG) treatment. High Treg counts were associated with female patients, older age, T1 category, and high tumor grade. TAM count was significantly correlated with Treg count and with IL6-positive cancer cell count. In our analysis of 71 patients treated with BCG, high counts of Treg and TAM were associated with shorter recurrence-free survival, and the former was an independent predictor of recurrence. Poor response to intravesical BCG was associated with Treg and TAM in the tumor microenvironment. Disrupting the immune network can be a supplementary therapeutic approach for NMIBC patients receiving intravesical BCG.
调节性 T 细胞(Treg)和肿瘤相关巨噬细胞(TAM)在人类膀胱癌肿瘤微环境中的临床意义尚不清楚。本研究旨在探讨它们与非肌肉浸润性膀胱癌(NMIBC)的肿瘤学特征的相关性。我们使用从 154 名 NMIBC 患者获得的手术标本,对叉头框 P3(FOXP3,Treg 标志物)、CD204(TAM 标志物)和白细胞介素-6(IL6)进行了免疫组织化学分析。评估了癌症病变周围的 Treg 和 TAM 计数以及 IL6 阳性癌细胞计数与临床病理变量的相关性。我们关注癌症病变周围 Treg 和 TAM 计数预测辅助膀胱内卡介苗(BCG)治疗后结局的能力。高 Treg 计数与女性患者、年龄较大、T1 类和高肿瘤分级相关。TAM 计数与 Treg 计数和 IL6 阳性癌细胞计数显著相关。在对 71 名接受 BCG 治疗的患者进行分析时,Treg 和 TAM 计数较高与无复发生存时间较短相关,前者是复发的独立预测因子。肿瘤微环境中 Treg 和 TAM 与膀胱内 BCG 反应不良有关。破坏免疫网络可能是接受膀胱内 BCG 治疗的 NMIBC 患者的辅助治疗方法。