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. 2016 May 19;5(7):e1188243. doi: 10.1080/2162402X.2016.1188243

Table 2.

Evaluation of immune cell subsets in colorectal cancer patients prior to and after 30 d of standard-of-care anticancer therapy.

  Baseline Post 30 d N
Number of PBMCs (x103/µL) 2.1 (1.9–2.6) 2.1 (1.5–2.7) 23
CD4+ T cells (%) 47 (31–53) 47 (39–52) 23
Number of CD4+ T cells (x103/µL) 0.9 (0.6–1.1) 1.0 (0.7–1.3) 23
CD8+ T cells (%) 24 (15–30) 22 (19–26) 23
Number of CD8+ T cells (x103/µL) 0.5 (0.4–0.8) 0.5 (0.3–0.6) 23
Treg of CD4+ T cells (%) 5.8 (4.7–8.0) 5.7 (4.6–6.7) 23
Treg of PBMCs (%) 2.6 (2.1–3.3) 2.6 (1.5–3.2) 23
Number of Tregs (x103/µL) 0.06 (0.04–0.07) 0.06 (0.03–0.07) 23
CD4+ Teff:Treg Ratio 17.0 (12.4–21.3) 17.6 (14.9–21.7) 23
CD8+ Teff:Treg Ratio 9.9 (6.1–15.0) 8.7 (5.7–16.0) 23
CD4+:CD8+ Ratio 1.9 (1.1–3.1) 2.0 (1.4–3.2) 23
Treg suppression (%) 44 (34.5–51) 39 (28.0–58.0) 13

Twenty-three first-line metastatic colorectal cancer patients were enrolled and treated with FOLFIRI therapy. PBMCs were collected at baseline and post 30 d of therapy, and subjected to flow cytometry analysis as described in Methods section. Values are the median (interquartile range). Wilcoxon test between baseline and post 30 d showed no statistical differences for any of the immune cell subsets studied, or for the Treg suppression assay.

PBMCs, peripheral blood mononuclear cells; Treg, regulatory T cells.