CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Expression of CD4+ and CD8+ Tumor-Infiltrating Lymphocytes in Oral Squamous Cell Carcinoma and Their Relationship With Clinicopathological Parameters: A Cross-Sectional Study.
Expression of CD4+ and CD8+ Tumor-Infiltrating Lymphocytes in Oral Squamous Cell Carcinoma and Their Relationship With Clinicopathological Parameters: A Cross-Sectional Study.
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口腔鳞状细胞癌(OSCC)是口腔最常见的恶性肿瘤。肿瘤微环境(TME)是由肿瘤和宿主共同组成的动态生态系统。TME 中的免疫细胞主要包括 CD4+ 和 CD8+ TIL(肿瘤浸润淋巴细胞),它们可抑制癌细胞增殖,在 OSCC 进展中发挥关键作用。本研究旨在分析 OSCC 中 CD4+ 和 CD8+ TIL 的免疫组织化学表达,并比较其与临床病理参数的关系。
对 75 份原发 OSCC 病例的福尔马林固定石蜡包埋样本进行 CD4+ 和 CD8+ 抗体免疫染色,并将其表达与临床病理参数进行比较。
CD4+ 与 CD8+ 表达显著正相关(r = 0.655,p = 0.001)。CD4+(r = -2.37,p = 0.041)和 CD8+(r = -0.348,p = 0.002)表达均与 OSCC 的 TNM 分期负相关(原文报告 r = -2.37,p = 0.041)。CD8+ 表达与组织病理学分级正相关(r = 0.288,p = 0.012)。
研究结果提示,CD4+ 细胞对维持和支持 CD8+ TIL 介导的抗肿瘤反应至关重要。CD4+ 和 CD8+ TIL 是细胞介导适应性免疫的关键参与者,可阻止肿瘤进展和转移。值得注意的是,尽管肿瘤中 CD8+ 浸润较多,肿瘤分级仍较高,这可能与癌症免疫编辑有关。
Background Oral squamous cell carcinoma (OSCC) is the most common malignant neoplasm of the oral cavity. The tumor microenvironment (TME) is a dynamic ecosystem composed of components contributed by both the tumor and the host. The immune cells of TME, mainly CD4+ and CD8+ tumor-infiltrating lymphocytes (TILs), suppress the proliferation of cancer cells and play a crucial role in the progression of OSCC. The present study aims to analyze the immunohistochemical expression of CD4+ and CD8+ TILs in OSCC and to compare and correlate them with clinicopathological parameters. Methodology A total of 75 formalin-fixed paraffin-embedded samples of cases diagnosed with primary OSCC were immunostained with CD4+ and CD8+ antibodies and their expression was compared with the clinicopathological parameters.
Results There was a significant positive correlation between CD4+ and CD8+ expression (r = 0. 655, p = 0. 001). Both CD4+ (r = -2. 37, p = 0. 041) and CD8+ (r = -0. 348, p = 0. 002) expressions negatively correlated with the TNM stage (r = -2. 37, p = 0. 041) of OSCC. CD8+ expression positively correlated with histopathological grade (r = 0. 288, p = 0. 012).
Conclusions The study findings suggest that CD4+ cells are essential to maintain and sustain CD8+ TIL-mediated anti-tumor response. CD4+ and CD8+ TILs are key players in cell-mediated adaptive immunity and prevent tumor progression and metastasis. Strikingly, the higher grade of tumors despite heavy CD8+ infiltration may possibly be due to cancer immunoediting.
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