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. 2018 Oct 8;74(1):152–164. doi: 10.1111/all.13479

Figure 3.

Figure 3

Epicutaneous immunotherapy (EPIT) does not modify the proportions of Th1 and Th2 cells, but increases Foxp3+ Tregs, CD62L+, and CD62L Tregs obtained from spleen. Gating strategy (A and D) and analysis of the proportions of Th2 (B), Th1 (C) after a short in vitro stimulation with PMA‐ionomycin, and Foxp3+ Tregs (E), Foxp3+ CD62L+ Tregs (F), and Foxp3+ CD62L Tregs (G) ex vivo after EPIT. For CD4+, IL4+, and IFNγ+ gates, the y‐axis was arbitrarily defined with a fluorochrome different from those used in the gating strategy and without any specific antibody (PerCP‐Cy5.5 or APR‐Cy7). Results are expressed as mean ± SD in percentage of total CD4+ T cells. Differences between groups were analyzed by a Mann‐Whitney test. *P < .05, ***P < .001