Department of Gynaecology and Gynaecological Oncology, Medical University of Gdańsk, Gdańsk, Poland.
Int J Gynecol Cancer. 2011 May;21(4):717-21. doi: 10.1097/IGC.0b013e3182131f36.
The clinicopathological significance of the local spontaneous immune reaction in vulvar squamous cell carcinoma remains unclear. The purpose of this study was to clarify the role of the subtypes of tumor-infiltrating lymphocytes, both individually and synergistically.
Seventy-six patients with verified histopathological data and complete clinical history were included into the study. We collected 76 paraffin-embedded samples of the primary tumor. The presence of CD4+ and CD8+ T cells was evaluated by immunohistochemistry and compared with commonly recognized prognostic factors. The primary end point analyzed was the overall survival.
CD4+ and CD8+ T cells were detected both within the nests of carcinoma and in the stroma, but only the infiltration within cancer cell nests was further analyzed. There was significant positive correlation (Spearman rho test R = 0.282, P = 0.014) between the number of intratumoral CD4+ and CD8+ T cells. No correlation was observed between the number of tumor-infiltrating CD4+ and CD8+ T cells and the patients' survival. Patients were classified into the following 4 groups (CD4+/CD8+, CD4⁻/CD8⁻ CD4+/CD8⁻, CD4⁻/CD8+), but none of them correlated with overall survival.
These data support the statement that CD4⁻ and CD8+ T cells cooperate within cancer cell nests, but this spontaneous immune reaction is an individual feature not influencing the prognosis. Intratumoral CD4+ T cells might control or reflect the immune responses against cancer cells, whereas CD8+ T cells do not seem to work as sufficient effectors in tumor tissues.
外阴鳞状细胞癌中局部自发性免疫反应的临床病理意义尚不清楚。本研究旨在阐明肿瘤浸润淋巴细胞亚群的作用,包括单独作用和协同作用。
本研究纳入了 76 例具有明确组织病理学数据和完整临床病史的患者。我们收集了 76 例原发性肿瘤的石蜡包埋样本。通过免疫组织化学评估 CD4+和 CD8+T 细胞的存在,并将其与公认的预后因素进行比较。分析的主要终点是总生存期。
CD4+和 CD8+T 细胞均存在于癌巢内和间质中,但仅对癌巢内浸润的细胞进行了进一步分析。肿瘤内 CD4+和 CD8+T 细胞数量之间存在显著正相关(Spearman rho 检验 R = 0.282,P = 0.014)。肿瘤浸润 CD4+和 CD8+T 细胞的数量与患者的生存无关。患者被分为以下 4 组(CD4+/CD8+、CD4⁻/CD8⁻、CD4+/CD8⁻、CD4⁻/CD8+),但均与总生存期无关。
这些数据支持以下观点,即 CD4⁻和 CD8+T 细胞在癌巢内相互协作,但这种自发性免疫反应是一种个体特征,不影响预后。肿瘤内 CD4+T 细胞可能控制或反映针对癌细胞的免疫反应,而 CD8+T 细胞似乎不能作为肿瘤组织中的有效效应物发挥作用。