Figure 3
From: The breast cancer immune microenvironment is modified by neoadjuvant chemotherapy

T cell composition in tumor and normal breast tissue. (A) Frequency of CD45+ cells from healthy donors (HD) and breast cancer patients (BCP). (B) Frequency of CD3+ cells from HD and BCP. (C) Frequency of CD3+ cells according to the molecular subtype of breast cancer: luminal A (LA), luminal B (LB), Her2 and triple negative (TN). (D) Percentage of CD4+ and CD8+ T cells. Distribution of memory subpopulations of CD4+ (E) and CD8+ T cells (F) evaluated using the CD45RA, CD62L, CCR7 and CD95 markers to define naïve (TN), stem cell memory (TSCM), central memory (TCM), tissue-resident memory-like (TRM), effector memory (TEM) and terminally differentiated effector (TTE) T cells. Pie charts of the distribution of CD4+ (G) and CD8+ T cell (H) memory subpopulations according to the molecular subtype of breast cancer. (I) Frequency of CD4+CD25+Foxp3+ regulatory T cells (Tregs). (J) Ratio of CD8+/Treg cells. (K) Frequency of CD4+ and CD8+ T cells from HD and patients with positive lymph nodes (PLNs) or negative lymph nodes (NLNs). (L) Treg frequency according to the lymph node state. (M) Frequency of follicular T cells from healthy donors (HD) and breast cancer patients (BCP). Data are represented as the mean ± SEM in (A, B, C, D, E, F, I, and J). Data are represented as violin plots, and lines indicate quartiles in K and J. The p values were calculated using a Mann–Whitney test. *p < 0.05, **p < 0.01, ***p < 0.001.