UMR INSERM, U892, Nantes, France.
PLoS One. 2010 Jan 5;5(1):e8437. doi: 10.1371/journal.pone.0008437.
Double positive (DP) CD4CD8 Talphabeta cells have been reported in normal individuals as well as in different pathological conditions including inflammatory diseases, viral infections and cancer, but their function remains to be elucidated. We recently reported the increased frequency of DP Talphabeta cells in human breast pleural effusions. This manuscript addresses the question of the existence and above all the role of this non-conventional DP sub-population among tumor associated lymphocytes in melanomas.
METHODOLOGY/PRINCIPAL FINDINGS: We analyzed the intratumoral cell infiltrate in solid metastasis (n = 6) and tumor invaded lymph nodes (n = 26) samples from melanomas patients by multiparametric cytometry. Here we documented for the first time significant increased frequency of DP T cells in about 60% of melanoma tumors compared to blood samples. Interestingly, a high proportion of these cells produced TNF-alpha in response to autologous melanoma cell lines. Besides, they are characterized by a unique cytokine profile corresponding to higher secretion of IL-13, IL-4 and IL-5 than simple positive T cells. In deep analysis, we derived a representative tumor-reactive DP T cell clone from a melanoma patient's invaded lymph node. This clone was restricted by HLA-A2402 and recognized both autologous and allogeneic tumor cells of various origins as well as normal cells, suggesting that the target antigen was a ubiquitous self antigen. However, this DP T cell clone failed to kill HLA-A2402 EBV-transformed B cells, probably due to the constitutive expression of immunoproteasome by these cells.
CONCLUSIONS/SIGNIFICANCE: In conclusion, we can postulate that, according to their broad tumor reactivity and to their original cytokine profile, the tumor associated DP T cells could participate in immune responses to tumors in vivo. Therefore, the presence of these cells and their role will be crucial to address in cancer patients, especially in the context of immunotherapies.
双阳性(DP)CD4CD8 Talphabeta 细胞已在正常个体以及炎症性疾病、病毒感染和癌症等不同病理情况下被报道,但它们的功能仍有待阐明。我们最近报道了人胸腔积液中 DP Talphabeta 细胞频率的增加。本文探讨了这种非传统 DP 亚群在肿瘤相关淋巴细胞中是否存在以及首先是在黑色素瘤中的作用。
方法/主要发现:我们通过多参数细胞术分析了黑色素瘤患者实体转移(n = 6)和肿瘤浸润淋巴结(n = 26)样本中的肿瘤内细胞浸润。在这里,我们首次记录到与血液样本相比,约 60%的黑色素瘤肿瘤中 DP T 细胞的频率显著增加。有趣的是,这些细胞中相当一部分在对自体黑色素瘤细胞系作出反应时产生 TNF-alpha。此外,它们的特征是独特的细胞因子谱,与简单阳性 T 细胞相比,它们分泌更高水平的 IL-13、IL-4 和 IL-5。在深入分析中,我们从黑色素瘤患者的浸润淋巴结中衍生出一个具有代表性的肿瘤反应性 DP T 细胞克隆。这个克隆受到 HLA-A2402 的限制,能够识别自体和异体来源的各种肿瘤细胞以及正常细胞,这表明靶抗原是一种普遍存在的自身抗原。然而,这个 DP T 细胞克隆未能杀死 HLA-A2402 EBV 转化的 B 细胞,可能是由于这些细胞组成型表达免疫蛋白酶体所致。
总之,根据其广泛的肿瘤反应性和原始的细胞因子谱,我们可以假设肿瘤相关的 DP T 细胞可能参与体内肿瘤的免疫反应。因此,这些细胞的存在及其作用将是癌症患者,尤其是在免疫治疗背景下,需要解决的关键问题。