Supplementary Materials

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  • Fig. S1. Leukocyte population changes in mice with OXZ-induced CHS.
  • Fig. S2. Treg cells are not essential for the development of IL-10+ Breg cells in peripheral tissues.
  • Fig. S3. The population changes in MCs, IL-13+ ILC2s, and IL-10+ Breg cells during OXZ-induced chronic atopic dermatitis (AD)–like skin inflammation.
  • Fig. S4. Comparison of MCs and Treg cells in WT and Cd19Cre mice with CHS.
  • Fig. S5. The treatment of IL-13 mAb suppresses OXZ-induced CHS in mice.
  • Fig. S6. Analysis of B cells, Treg cells, and serum antibody isotypes from WT or KitW-sh/W-sh mice.
  • Fig. S7. CD40L on MCs is not critical for the suppression of CHS.
  • Fig. S8. Amounts of TH1 and TH2 cytokines in peripheral tissues from WT or KitW-sh/W-sh mice.
  • Fig. S9. The tissue distribution of MCs in KitW-sh/W-sh mice and Breg cells in Cd19Cre mice after the adoptive transfer of each cell.
  • Fig. S10. The sorting strategies for B cell subsets, IL-13+ ILC2s, and IL-10+ B cells.

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