This study investigated the distribution of interleukin (IL)-17-producing CD4(+) T-cells (T-helper [Th17] cells) in relation to CD4(+)CD25(+)CD127(-) cells (regulatory T-cells [T(reg)]) in tumour-infiltrating lymphocytes (TILs) and peripheral blood mononuclear cells (PBMCs) from breast cancer patients. The Th17 and T(reg) cells were evaluated by flow cytometry and reported as a percentage of total CD4(+) cells. In TILs from early breast cancer patients (n = 12), the frequency of Th17 cells was significantly higher than in PBMCs (14.5 ± 7.2% versus 6.9 ± 2.1%). In TILs from patients with advanced breast cancer (n = 15), the frequency of Th17 cells was also significantly higher than that in PBMCs (9.1 ± 5.7% versus 3.2 ± 2.3%) but lower compared with early disease. The Th17/T(reg) ratio in TILs was markedly increased in early versus advanced disease. In conclusion, Th17 and T(reg) cell accumulation in the tumour microenvironment of breast cancer occurred in early disease; Th17 cell infiltration gradually decreased and T(reg) cells accumulated with disease progression.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2011) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: