Tavana Shirin, Mokhtari Zahra, Sanei Mohammad Hossein, Heidari Zahra, Dehghanian Amir-Reza, Faghih Zahra, Rezaei Marzieh
Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 8174673461, Iran.
Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Cancer Cell Int. 2023 Feb 10;23(1):23. doi: 10.1186/s12935-023-02864-3.
It is well-documented that the interplay between tumor-infiltrating lymphocytes (TILs) and tumor cells is a major determining factor in cancer progression. CD45RO seems to be a reliable indicator for predicting prognosis and disease outcome, along with CD3 and CD8 markers. LAG-3 is another important marker that overexpresses on TILs in a variety of cancers and is associated with disease prognosis; however, its prognostic impact is controversial. Hence, in the present study, we aimed to investigate the presence of CD45RO + , LAG3 + , CD3 + , and CD8 + lymphocytes in CRC tumor tissues and their association with clinicopathological parameters of the disease as well as patients' survival, according to primary tumor locations.
Expression of CD45RO, LAG3, CD3, and CD8 was immunohistochemically assessed in tissue sections of 136 patients with CRC. The percentages of TILs expressing these markers were then separately determined in both invasive margin (IM) and center of tumor (CT). Their associations with clinicopathological factors and patients' survival were analyzed in the entire cohort and the subgroups of patients with right- and left- rectum tumors.
Based on our observation, CD45RO + and CD3 + cells were the most frequent infiltrated lymphocytes in both CT and IM regions of colon tumor tissue. Whilst, LAG3 + lymphocytes were the least frequent subset in both areas. Statistical analysis indicated that the frequency of CD45RO + TILs was positively associated with advanced TNM stages (III/IV), in the entire cohort and right-sided tumors (P < 0.05). LAG3 + TILs in IM were also increased in tumor tissues with higher T-stages in the entire cohort (P = 0.027). In univariate analysis, high score of CD45RO + TILs in IM was associated with better overall survival in the entire cohort. High score of CD8 + and CD45RO + lymphocytes in IM were also associated with improved survival in patients with right-sided tumors.
Our findings generally suggest that the clinicopathological and prognostic significance of immune system-related markers such as CD45RO and LAG3 depends on the primary tumor sides. Our results collectively demonstrated that infiltration of CD45RO + lymphocytes in IM could be an independent prognostic factor in a site-dependent manner.
肿瘤浸润淋巴细胞(TILs)与肿瘤细胞之间的相互作用是癌症进展的主要决定因素,这一点已有充分记录。CD45RO与CD3和CD8标志物一样,似乎是预测预后和疾病结局的可靠指标。LAG-3是另一个重要标志物,在多种癌症的TILs上过度表达,与疾病预后相关;然而,其预后影响存在争议。因此,在本研究中,我们旨在根据原发性肿瘤位置,调查结直肠癌(CRC)肿瘤组织中CD45RO +、LAG3 +、CD3 +和CD8 +淋巴细胞的存在情况,以及它们与该疾病临床病理参数和患者生存率的关系。
对136例CRC患者的组织切片进行免疫组织化学评估,检测CD45RO、LAG3、CD3和CD8的表达。然后分别在浸润边缘(IM)和肿瘤中心(CT)确定表达这些标志物的TILs百分比。在整个队列以及右半直肠和左半直肠肿瘤患者亚组中分析它们与临床病理因素和患者生存率的关系。
根据我们的观察,CD45RO +和CD3 +细胞是结肠肿瘤组织CT和IM区域中最常见的浸润淋巴细胞。而LAG3 +淋巴细胞是这两个区域中最不常见的亚群。统计分析表明,在整个队列和右侧肿瘤中,CD45RO + TILs的频率与晚期TNM分期(III/IV)呈正相关(P < 0.05)。在整个队列中,T分期较高的肿瘤组织中IM区域的LAG3 + TILs也增加(P = 0.027)。在单因素分析中,IM区域CD45RO + TILs高分与整个队列中更好的总生存率相关。IM区域CD8 +和CD45RO +淋巴细胞高分也与右侧肿瘤患者生存率提高相关。
我们的研究结果总体表明,CD45RO和LAG3等免疫系统相关标志物的临床病理和预后意义取决于原发性肿瘤的部位。我们的结果共同表明,IM区域CD45RO +淋巴细胞浸润可能是以部位依赖的方式成为一个独立的预后因素。