CXCR5 + CD8 T cells displayed higher activation potential despite high PD-1 expression, in tumor-involved lymph nodes from patients with thyroid cancer

摘要

Thyroid cancer is one of the malignancies with better clinical outcomes. However, a minority of patients develops an aggressive anaplastic thyroid carcinoma. Development of innovative and multimodal therapeutic strategies is urgently needed. Here, we investigated the role of CXCR5+CD8 T cells in the peripheral blood, tumor-involved lymph nodes (TILN), and tumor mass of thyroid cancer patients. In peripheral blood mononuclear cells, CXCR5+cells represented 1.4%?±?0.84% (mean?±?s.d.) of total CD8 T cells, while in TILN and in tumor, the frequencies of CXCR5+CD8 T cells were significantly higher at 27.7%?±?7.8% and 15.5%?±?2.9%, respectively. Compared to CXCR5?CD8 T cells, CXCR5+CD8 T cells presented significantly higher PD-1 expression and lower or comparable TIM-3 and CTLA-4 expression. To compare and contrast the functional characteristics of CXCR5+CD8 T cells and CXCR5?CD8 T cells, these cells were separated from TILNs and were TCR-stimulated via anti-CD3/CD28. Upon stimulation, CXCR5+CD8 T cells presented stronger downregulation of CD27, higher expression of proinflammatory cytokines IL-2, IFN-γ, and TNF-α, and higher proliferation capacity than CXCR5?CD8 T cells. Moreover, CXCR5+CD8 T cells presented higher expression of cytotoxic molecules Gzm-A, Gzm-B, and perforin. Overall, these results demonstrated that in thyroid cancer patients CXCR5+CD8 T cells infiltrated the TILNs and the tumors, and were functionally more potent compared to their CXCR5?counterpart.