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The subsets of dendritic cells and memory T cells correspond to indoleamine 2,3-dioxygenase in stomach tumor microenvironment
Authors:Fangxuan Li  Jinchao Huang  Shixia Li  Hui Li  Jinpu Yu  Xiubao Ren  Juntian Liu
Affiliation:1. Cancer Prevention Center, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China
2. Department of Immunology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China
Abstract:The abnormal distributions of memory T cells (Tm) and dendritic cells (DC) in stomach cancer are not well understood. Indoleamine 2,3-dioxygenase (IDO), produced by DC, may be an important enzyme affecting function and proliferation of Tm. In this study, IDO expression was examined by immunohistochemical staining. The subsets of Tm and DC were counted by flow cytometry. The percentages of CD4?+?Tm and CD4?+?central Tm (Tcm) were lower in tumor tissues than in normal tissues (P?P?P?=?0.009). The high expression of IDO was more frequently observed in tumor tissues (P?=?0.001). The percentages of CD4?+?Tm and CD8?+?Tm were positively associated with DC1 percentage and ratio of DC1/DC2 (P?P?=?0.025). The patients with high IDO expression had significantly lower CD4?+?Tm (P?=?0.012) and CD8?+?Tm percentages (P?=?0.033), but higher CD8?+?Tem percentage (P?P?=?0.019). The CD4?+?Tm and CD8?+?Tem percentages were significantly associated with clinical stage and lymph node metastasis; the high IDO expressions were significantly associated with deeper tumor invasion (P?=?0.016) and lymph node metastasis (P?=?0.038). Thus, DC subsets, Tm subsets, and IDO expression were correlated with each other. They were associated with the established clinicopathologic features, such as tumor size, depth of invasion, lymph node metastasis, and clinical stage.
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