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. 2018 Apr 12;164(1):313–327. doi: 10.1093/toxsci/kfy091

Table 4.

TCE Promoted Th1/Th17 Phenotype

TCE TCE TCE+ TCE+ (1) (1) (1) (2) (2) (3)
HFD HFD+ HFD HFD+ vs vs vs vs vs vs
(1) (2) (3) (4) (2) (3) (4) (3) (4) (4)
ifng 33.2 (13.0) 43.4 (19.8) 65.8 (34.5) 78.6 (11.9) 0.8 0.08 0.02 0.4 0.1 0.8
Il17 21.7 (14.1) 17.5 (15.4) 41.8 (26.0) 111 (77.9) 0.9 0.8 0.008 0.8 0.01 0.06
Il4 692.6(1441.3) 329.3 (507.9) 799.6 (543.2) 227.2 (189.7) 0.03 0.2 0.008 0.8 0.9 0.4
tnfa 4.1 (1.8) 26.7 (28.2) 12.1 (6.1) 15.4 (7.3) 0.07 0.8 0.7 0.4 0.7 0.9

Splenic CD4+ T cells were isolated and activated as described in the “Materials and Methods” section. Cells were harvested and processed for RNA and cytokine expression was measured by qRT-PCR. Numbers represent mean and SD fold change values relative to unstimulated CD4+ T cells and normalized by EEF2 housekeeping gene. Data were analyzed by 2-way ANOVA to test for interaction and main effects of the 2 variables (TCE and HFD). Numbers represent mean and SD of the 4 exposure groups (1–4). Data were analyzed by 2-way ANOVA to test for significant interaction of the 2 variables (TCE × HFD). Shown in the table are p values for the 6 pairwise Tukey’s post hoc comparisons numbered by group and conducted as described in the “Materials and Methods” section. Results are statistically significant (p < .05) indicated in bold.