Figure 2.
Figure 2. Frequency and immune phenotype of Vγ9Vδ2-T cells in CLL patients and HCs. Immunophenotyping of Vγ9Vδ2-T cells from untreated CLL patients and age-matched HCs, directly ex vivo. (A) Frequency of Vγ9+Vδ2+ cells within CD3+ T lymphocytes (CLL, n = 39; HC, n = 20). (B) Absolute number of Vγ9Vδ2-T cells (CLL, n = 39; HC, n = 6). (C) Distribution of differentiation subsets within Vγ9Vδ2-T cells based on CD27 and CD45RA expression (CLL, n = 39; HC, n = 20). (D) Expression of exhaustion markers on Vγ9Vδ2-T cells. Geometric mean fluorescence intensity (gMFI) of PD-1 and BTLA expression (CLL, n = 39; HC, n = 20) and CD244, CD160, and LAG-3 expression (CLL, n = 16; HC, n = 11). (E) Frequency of granzyme B+ and granzyme K+ cells within Vγ9Vδ2-T cells (CLL, n = 7; HC, n = 7). Data are mean and SEM. *P < .05, Student t test. TCM, CD27+CD45RA−; TEM, CD27−CD45RA−; TEMRA, CD27−CD45RA+; TN, CD27+CD45RA+.

Frequency and immune phenotype of Vγ9Vδ2-T cells in CLL patients and HCs. Immunophenotyping of Vγ9Vδ2-T cells from untreated CLL patients and age-matched HCs, directly ex vivo. (A) Frequency of Vγ9+Vδ2+ cells within CD3+ T lymphocytes (CLL, n = 39; HC, n = 20). (B) Absolute number of Vγ9Vδ2-T cells (CLL, n = 39; HC, n = 6). (C) Distribution of differentiation subsets within Vγ9Vδ2-T cells based on CD27 and CD45RA expression (CLL, n = 39; HC, n = 20). (D) Expression of exhaustion markers on Vγ9Vδ2-T cells. Geometric mean fluorescence intensity (gMFI) of PD-1 and BTLA expression (CLL, n = 39; HC, n = 20) and CD244, CD160, and LAG-3 expression (CLL, n = 16; HC, n = 11). (E) Frequency of granzyme B+ and granzyme K+ cells within Vγ9Vδ2-T cells (CLL, n = 7; HC, n = 7). Data are mean and SEM. *P < .05, Student t test. TCM, CD27+CD45RA; TEM, CD27CD45RA; TEMRA, CD27CD45RA+; TN, CD27+CD45RA+.

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