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Involvement of Indoleamine 2,3-Dioxygenase in Impairing Tumor-Infiltrating CD8+ T-Cell Functions in Esophageal Squamous Cell Carcinoma

机译:吲哚胺2,3-双加氧酶参与食管鳞状细胞癌中肿瘤浸润CD8 + T细胞功能的损害。

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摘要

The indoleamine 2,3-dioxygenase-(IDO-) mediated microenvironment plays an important role in tumor immune escape. However, the inhibitory effects of IDO on the CD8+ tumour-infiltrating lymphocytes (CD8+ TILs) in esophageal squamous cell carcinoma (ESCC) have not been clarified yet. Here, we found that the level of IDO expression in ESCC tumor specimens correlated with a reduction in the number of CD8+ TILs. Patients with high IDO expression and a low number of CD8+ TILs had significantly impaired overall survival time. IDO expression and functional enzyme activity in ESCC cell lines could be induced by IFNγ. When exposed to the milieu generated by IDO-expressing Eca109 cells, the CD8+ TILs were suppressed in proliferation, and their cytolytic functions against target tumor cells were lost. These results suggested that impairing CD8+ TIL functions by IDO expressed in ESCC possibly contributed to the finding that patients with higher IDO expression have more aggressive disease progression and shorter overall survival time.
机译:吲哚胺2,3-二加氧酶-(IDO-)介导的微环境在肿瘤免疫逃逸中起重要作用。但是,IDO对食管鳞状细胞癌(ESCC)中CD8 +肿瘤浸润淋巴细胞(CD8 + TILs)的抑制作用尚未阐明。在这里,我们发现ESCC肿瘤标本中IDO表达的水平与CD8 + TIL数量的减少有关。具有高IDO表达和少量CD8 + TIL的患者严重损害了总生存时间。 IFNγ可诱导ESCC细胞株的IDO表达和功能酶活性。当暴露于表达IDO的Eca109细胞产生的环境中时,CD8 + TILs的增殖受到抑制,并且丧失了针对靶肿瘤细胞的溶细胞功能。这些结果表明,在ESCC中表达的IDO损害CD8 + TIL功能可能有助于发现具有较高IDO表达的患者具有更积极的疾病进展和更短的总生存时间。

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