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. Author manuscript; available in PMC: 2014 Aug 22.
Published in final edited form as: Immunity. 2013 Aug 8;39(2):10.1016/j.immuni.2013.07.014. doi: 10.1016/j.immuni.2013.07.014

Figure 4.

Figure 4

The fate of a single clone is distinct between the spleen and the intestinal mucosa. a. Stacked graphs of the phenotype of the progeny of 9 transferred OVA-specific clones (present in 20 mice) seven days after VSV-OVA infection in both spleen (S) and peripheral LN (L). Peripheral lymph nodes include axial, brachial, and inguinal. b. Stacked graphs of the phenotype of the progeny of 8 transferred OVA-specific clones found 10 days after oral LM-OVA infection in both the spleen (S) and intestinal epithelium (I). The first set of stacked graphs represents the average distribution of effector populations in the bulk host response of all 20 mice in each experiment. This experiment was repeated twice with similar results.