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. 2013 May 1;8(5):e63100. doi: 10.1371/journal.pone.0063100

Figure 2. Evaluation of the capacity of F4/80+CD11b+, F4/80lowCD11b+ and MHCII+CD11chigh populations to produce TNF-α and IL-12/IL-23p40 during the acute phase of T.cruzi infection.

Figure 2

Splenic cells were analyzed seven days post-infection. (A) Representative flow cytometry plots showing the exclusion of debris and non-interest population of interest (FSC-H X SSC-H) and the assortment of immune cells from non-infected or infected mice. Representative flow cytometry plots showing intracellular cytokine in the different cells from non-infected or infected mice. (B) Frequencies of IL-12/IL-23p40+ or TNF-α+ splenic cells (F4/80+CD11b+, F4/80lowCD11b+ or MHCII+CD11chigh) (mean ± SD of four mice) isolated from non-infected or infected mice. Data are representative of two independent experiments. **p<0.01 indicates statistical significance when comparing the percentage of the same cell population from infected versus non infected mice involved in TNF-α or IL-12/IL-23p40 production.