Fig. 1From: High co-expression of immune checkpoint receptors PD-1, CTLA-4, LAG-3, TIM-3, and TIGIT on tumor-infiltrating lymphocytes in early-stage breast cancerFlow cytometric analysis of TILs subsets. A representative example of the flow cytometric gating strategy used for the immune checkpoint receptor analysis of NK cell subsets and cytotoxic T cells is shown. Tumor infiltrated lymphocytes were identified by their size and granularity in the FSC/SSC dot plot, and NK cells were gated on the SSC/CD3- and then gated further as CD56bright or CD56dim NK cells. Cytotoxic T cells were identified by gating on CD3+/CD8+ quadrant. PD-1, TIGIT, CTLA-4, LAG-3, and Tim-3 expressions were evaluated on CD8+ T cells and cytotoxic (CD16+CD56dim) and cytokine secreting (CD16-CD56bright) NK cells. PD-1, TIGIT, CTLA-4, LAG-3, and Tim-3 expressions are given as percentage of the designated population. Data were analyzed using the FlowJoTM10.2 softwareBack to article page