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. Author manuscript; available in PMC: 2014 Mar 1.
Published in final edited form as: Cancer Prev Res (Phila). 2013 Jan 15;6(3):242–252. doi: 10.1158/1940-6207.CAPR-12-0320

Table 1.

Effect of co-culture of dendritic cells from wild-type and XPA-KO mice with CD4+ T cells on cytokine production

Cytokines Wild-type
XPA-KO
Control UV GSPs +UV Control UV GSPs+ UV
IFNγ 320 152 (53) 353 (132)* 212 131 (38) 152
IL-4 215 296 (38) 197 (33)* 208 328 (57) 250
IL-10 456 844 (85) 659 (22)* 308 532 (73) 487

Dendritic cells were isolated from the draining lymph nodes of different treatment groups, as described in Materials and Methods. CD4+ T cells isolated from the spleens of naïve wild-type mice were labeled with CFSE and co-cultured with CD11c+ cells in the ratio of 10:1 for 4 days. Cells were harvested, and cell supernatants were subjected to the analysis of cytokines by ELISA. Values in parentheses under UV-exposed groups indicate percent reduction (IFNγ) or percent increase (IL-4, IL-10) in the amount of cytokines secreted by CD4+ T cells compared to controls. Asterisks (*) indicate that co-culture of DCs from GSPs-treated wild-type mice with CD4+ T cells enhanced the production of IFNγ (132%) and reduced the production of IL-4 (33%) and IL-10 (22%) compared to non-GSPs-treated UVB-irradiated mice in wild-type group. Cytokine concentration is reported in terms of mean values and pg/2 million cells, n=2. Standard deviation to mean values of cytokine content was in the range of 4-8% in each group.