Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, Jordan.
Eur Rev Med Pharmacol Sci. 2022 Jun;26(12):4207-4219. doi: 10.26355/eurrev_202206_29057.
Though tumor-infiltrating lymphocytes (TILs) have a predictive impact in cancer patients, their association with presentation and prognosis in breast cancer is less consistent. This study aimed to assess the level of infiltrating cytotoxic T lymphocytes (CTLs) and regulatory T lymphocytes (Tregs) and their association with the clinicopathological features of breast cancer.
Tissue samples from female patients (n=153) diagnosed with primary invasive breast cancer were stained with CD8 (a CTL marker) and Foxp3 (a Treg marker) using immunohistochemistry.
CTLs were distributed between tumor bed and stroma whereas Treg cells were mainly located in the stroma. The level of intratumoral CTLs correlated positively with Tregs in both tumor and stroma (rho=0.312, p<0.001 and rho=0.176, p=0.031; respectively). Stromal CTLs correlated positively with stromal Tregs (rho=0.319, p=0.005). Tumor size correlated inversely with the number of Treg cells in the tumor bed (rho= - 0.179, p=0.028). Tregs were associated with lymphovascular invasion status in the tumor bed (p=0.042). The ratio of intratumoral CTLs to Tregs was associated with estrogen receptor positivity and luminal subtype (p=0.029 and p=0.045, respectively). The median number of CTLs was significantly lower in patients using aspirin or antihypertensive medications compared to nonusers (p=0.024 and p=0.03, respectively).
TILs were distributed differently in tumor tissues of breast cancer patients. CTLs infiltrates were found in both tumor bed and stroma while Tregs were dominant in the stroma. TILs were also distinctly associated with tumor features. The impact of TILs on prognosis and treatment outcomes in Jordanian breast cancer patients needs further investigation.
尽管肿瘤浸润淋巴细胞(TILs)对癌症患者具有预测作用,但它们与乳腺癌的表现和预后的关系并不一致。本研究旨在评估浸润性细胞毒性 T 淋巴细胞(CTLs)和调节性 T 淋巴细胞(Tregs)的水平,并评估其与乳腺癌临床病理特征的关系。
使用免疫组织化学法对 153 名女性原发性浸润性乳腺癌患者的组织样本进行 CD8(CTL 标志物)和 Foxp3(Treg 标志物)染色。
CTL 分布于肿瘤床和基质之间,而 Treg 细胞主要位于基质中。肿瘤内 CTLs 水平与肿瘤和基质中的 Tregs 呈正相关(rho=0.312,p<0.001 和 rho=0.176,p=0.031;分别)。基质 CTLs 与基质 Tregs 呈正相关(rho=0.319,p=0.005)。肿瘤大小与肿瘤床中 Treg 细胞数量呈负相关(rho=-0.179,p=0.028)。Tregs 与肿瘤床中的淋巴血管侵犯状态有关(p=0.042)。肿瘤内 CTLs 与 Tregs 的比值与雌激素受体阳性和腔型亚型有关(p=0.029 和 p=0.045,分别)。与未使用者相比,使用阿司匹林或抗高血压药物的患者 CTLs 浸润的中位数明显较低(p=0.024 和 p=0.03,分别)。
TILs 在乳腺癌患者的肿瘤组织中分布不同。CTLs 浸润存在于肿瘤床和基质中,而 Tregs 则在基质中占主导地位。TILs 也与肿瘤特征明显相关。TILs 对约旦乳腺癌患者的预后和治疗结果的影响需要进一步研究。