CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Inverse Regulation of TLR4 and PD-L1 Shapes the Inflammatory Tumor Microenvironment in Oral Squamous Cell Carcinomas.
Inverse Regulation of TLR4 and PD-L1 Shapes the Inflammatory Tumor Microenvironment in Oral Squamous Cell Carcinomas.
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这些发现综合表明,PD-L1 或 TLR4 的激活协调免疫反应存在差异性调控,影响 T 细胞反应。
肿瘤微环境(TME)中恶性细胞与免疫细胞之间的相互作用显著影响癌症的发生和进展。本研究旨在分析TLR4和PD-L1的表达与口腔鳞状细胞癌(OSCC)免疫反应、临床特征及预后的相关性并进行关联分析。
我们的回顾性多中心研究包括对166例OSCC标本进行TLR4、PD-L1、CD8和Ki-67表达的评估,采用基于TMA的免疫组化分析。
我们的研究结果表明,PD-L1与TLR4的表达呈负相关(浅表肿瘤部位:r = -0.348,p = 0.014;总体分析:r = -0.269,p = 0.049)。另一方面,深部和浅表浸润前沿的PD-L1表达与CD8+ TTIL(肿瘤浸润淋巴细胞)呈正相关,且具有统计学显著性。在初次OSCC诊断后至少5年随访中,进行了逻辑回归分析以评估各变量对临床结局的影响。多变量模型显示,晚期T分期(T3-T4)、存在淋巴结转移(N+)以及接受化疗与OSCC死亡率具有统计学显著相关性。
The interactions between malignant cells and immune cells within the tumor microenvironment (TME) significantly influence cancer development and progression. This study aimed to analyze and correlate the expression of TLR4 and PD-L1 with the immune response, clinical characteristics, and prognosis of oral squamous cell carcinomas (OSCC).
Our retrospective multicentric study consisted of the assessment of 166 OSCC specimens for TLR4, PD-L1, CD8, and Ki-67 expression in a TMA-based immunohistochemistry analysis.
Our findings indicated an inverse correlation between the expression of PD-L1 and TLR4 (r = -0.348, p = 0.014, and r = -0.269, p = 0.049, superficial tumor site and in overall analysis, respectively). On the other hand, PD-L1 expression in the deep and superficial invasive front positively correlated with CD8+ T tumor infiltrating lymphocytes (TIL) in a statistically significant manner. A logistic regression analysis was performed to assess the impact of each variable on the clinical outcome with at least 5-year follow-up after the initial OSCC diagnosis. The multivariate model revealed that advanced T stage (T3-T4), presence of lymph node metastasis (N+), as well as performing chemotherapy were statistically significantly associated with OSCC mortality.
These findings taken together suggest that there is a differential regulation of the immune response coordinated by activation of PD-L1 or TLR4 affecting T cell response.
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