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. Author manuscript; available in PMC: 2013 Aug 31.
Published in final edited form as: Science. 2012 Jul 26;337(6098):1115–1119. doi: 10.1126/science.1225152

Fig. 2.

Fig. 2

Distinct commensal niches control T cell cytokine production in the gut and skin. (A) Taxonomic classifications at the phylum level for 16S ribosomal RNA gene sequence data clustered at 97% identity from skin tissue and fecal pellet of control mice and mice treated with oral antibiotic cocktail (ATB) for 4 weeks. Each column represents an individual mouse. (B) Assessment of IFN-γ production in live CD45+ TCRβ+ cells and IL-17A production in live CD45+ cells from skin and intestine of mice treated with oral antibiotic cocktail or water (Ctrl) for 4 weeks. Graphs show means ± SEM of four mice (**P < 0.005, ***P < 0.0005; ns, not significant). Results are representative of two or three experiments. (C and D) Flow cytometric analysis of IL-17A production in live CD45+ TCRβ+ cells from the gut and skin of SPF mice, GF mice, and GF mice monoassociated with S. epidermidis (GF + S.epi) for 2 to 3 weeks. Graphs show means ± SEM of three to five mice (**P < 0.005). Results are representative of two experiments.