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. 2013 May 29;2(4):478–487. doi: 10.1002/cam4.89

Flow-cytometric assessment of regulatory T cells

Treatment WEHI-164 K7M2
CD4+CD25+ (% ± SE) FoxP3+CD25+ (% ± SE) CD4+CD25+ cell no. (×106) ± SE CD4+CD25+ (% ± SE) FoxP3+CD25+ (% ± SE) CD4+CD25+ cell no. (×106) ± SE
Naive 4.8 ± 0.7 4.38 ± 0.06 0.21 ± 0.04 4.8 ± 0.7 4.38 ± 0.06 0.21 ± 0.04
Untreated 6.0 ± 0.9 5.30 ± 0.2 0.37 ± 2.6 7.0 ± 0.2 5.90 ± 0.3 0.44 ± 0.3
G-G 4.9 ± 0.6 3.70 ± 0.5 0.06 ± 0.9*** 4.6 ± 0.3 2.70 ± 0.2 0.29 ± 0.2***
L-M 4.1 ± 0.1 2.30 ± 0.9 0.09 ± 0.2*** 3.7 ± 0.3 3.05 ± 0.5 0.28 ± 0.2***
G-L-M-G 4.3 ± 0.3 3.00 ± 0.2 0.06 ± 0.9*** 5.1 ± 0.3 4.50 ± 0.1 0.32 ± 0.2***
L-M-G-G 2.4 ± 0.3 2.54 ± 0.8 0.08 ± 0.6*** 4.1 ± 0.3 3.20 ± 0.5 0.21 ± 0.1***

CD4+CD25+ Treg cells assessment in tumor-draining lymph nodes after therapeutic treatments.

The modulation of CD4+CD25+ and FoxP3+CD25+ double-positive Treg cells from tumor-draining lymph nodes was evaluated in naive-treated or untreated WEHI-164 and K7M2 tumor-bearing mice 3 days after the term of all the therapeutic treatments. The results are indicated in percentage (%) form and absolute number (cell no.) (mean ± SE). Data are representative for at least three mice belonging to the treatment group.

***

***P ≤ 0.001; **P ≤ 0.01; *P ≤ 0.05.