Skip to main content
. Author manuscript; available in PMC: 2020 Mar 1.
Published in final edited form as: Eur J Immunol. 2019 Jan 15;49(3):398–412. doi: 10.1002/eji.201847935

Figure 4.

Figure 4.

Helios and Helios+ Treg protect mice from IBD. CD4+RFPCD45RBhi T cells from 8–12 week old CD45.1 mice were injected r.o. into 8–10 week old B6.SJL RAG−/− recipients. Helios or Helios+ Treg from congenically marked (CD45.2) reporter mice were co-injected where indicated. (A) Mice were monitored weekly for weight loss. Data shown as mean percent weight change from original weight, representative of four independent experiments with n=5 mice per experiment. (B) Effector cells (CD4+TCRβ+CD45.1+) from the mesenteric lymph node were analyzed at 10–11 wks by intracellular staining for cytokine production. Data shown as mean ± SD, representative of four independent experiments with n=5 mice per experiment. (C) Treg cells (CD4+ TCRβ+CD45.2+) were quantified at 10–11 wks from the mesenteric node (left), were analyzed for RFP (Foxp3) expression (middle) and total Foxp3+ Treg calculated (right). Data shown as mean ± SD, representative of four independent experiments with n=5 mice per experiment. (D) Foxp3+ Treg in (C) were analyzed for Helios expression. Data shown as the percent of CD4+ TCRβ+CD45.2+ Foxp3+ cells that express Helios. Data shown as mean ± SD, representative of four independent experiments with n=5 mice per experiment (left) or a representive histogram.