Reissfelder Christoph, Stamova Slava, Gossmann Christina, Braun Marion, Bonertz Andreas, Walliczek Ute, Grimm Mario, Rahbari Nuh N, Koch Moritz, Saadati Maral, Benner Axel, Büchler Markus W, Jäger Dirk, Halama Niels, Khazaie Khashayarsha, Weitz Jürgen, Beckhove Philipp
J Clin Invest. 2015 Feb;125(2):739-51. doi: 10.1172/JCI74894. Epub 2014 Dec 22.
The composition of tumor-targeted T cell infiltrates is a major prognostic factor in colorectal cancer (CRC) outcome; however, the functional role of these populations in prolonging patient survival remains unclear. Here, we evaluated 190 patients with CRC for the presence of functionally active tumor-infiltrating lymphocytes (TILs), the tumor specificity of these TILs, and the correlation between patient TILs and long-term survival. Using intracytoplasmic cytokine staining in conjunction with HLA multimers loaded with tumor peptide and antigen-specific cytokine secretion assays, we determined that TNF-α expression delineates a population of tumor antigen-specific (TA-specific) cytotoxic T lymphocytes (CTLs) present within tumors from patients with CRC. Upregulation of TNF-α expression in TILs strongly correlated with an increase in the total amount of intratumoral TNF-α, which is indicative of tumor-specific CTL activity. Moreover, a retrospective multivariate analysis of 102 patients with CRC, which had multiple immune parameters evaluated, revealed that increased TNF-α concentration was an independent prognostic factor. Together, these results indicate that the prognostic impact of T cell infiltrates for CRC maybe largely based on subpopulations of active TA-specific T cells within the tumor, suggesting causal implication for these cells in patient survival. Additionally, these results support the use of intratumoral TNF-α, which is indicative of T cell function, as a prognostic parameter for CRC.
肿瘤靶向性T细胞浸润的组成是结直肠癌(CRC)预后的主要因素;然而,这些细胞群在延长患者生存期方面的功能作用仍不清楚。在此,我们评估了190例CRC患者,检测其是否存在功能活跃的肿瘤浸润淋巴细胞(TILs)、这些TILs的肿瘤特异性,以及患者TILs与长期生存之间的相关性。通过结合使用胞浆内细胞因子染色、负载肿瘤肽的HLA多聚体和抗原特异性细胞因子分泌检测,我们确定TNF-α表达可界定CRC患者肿瘤内存在的一群肿瘤抗原特异性(TA特异性)细胞毒性T淋巴细胞(CTLs)。TILs中TNF-α表达上调与肿瘤内TNF-α总量增加密切相关,这表明肿瘤特异性CTL活性增强。此外,对102例评估了多个免疫参数的CRC患者进行的回顾性多变量分析显示,TNF-α浓度升高是一个独立的预后因素。这些结果共同表明,T细胞浸润对CRC的预后影响可能很大程度上基于肿瘤内活跃的TA特异性T细胞亚群,提示这些细胞与患者生存存在因果关系。此外,这些结果支持将指示T细胞功能的肿瘤内TNF-α用作CRC的预后参数。