Figure 5
Figure 5. Plant-based oral tolerance induces CD4+CD25+ Tregs and LAP+CD25−CD4+ Tregs. (A) Experimental outline of adoptive transfer. CD4−, CD4+CD25−, and CD4+CD25+ cells were purified via magnetic sorting from spleens and MLNs of FIX-fed/intravenously challenged hemophilia B mice and pooled. Doses of 106 cells per mouse were adoptively transferred into strain-matched mice via tail vein injection. Control cells were from naive mice. After 24 hours, all recipient mice (n = 5-8 per group) were challenged with 1 IU FIX in adjuvant via subcutaneous injection. IgG titers against FIX (B) were determined 3 weeks later. (C) Purified CD4+CD25− cells were further divided into LAP+ and LAP− cells via magnetic sorting. The cells were adoptively transferred (n = 4-6 per group), followed by immunization with FIX. IgG titers against FIX (D) were determined 3 weeks later. Control mice had received cells from naive mice. Data are average ± SEM. Shown are data from 2 independent experiments that showed similar results.

Plant-based oral tolerance induces CD4+CD25+ Tregs and LAP+CD25CD4+ Tregs. (A) Experimental outline of adoptive transfer. CD4, CD4+CD25, and CD4+CD25+ cells were purified via magnetic sorting from spleens and MLNs of FIX-fed/intravenously challenged hemophilia B mice and pooled. Doses of 106 cells per mouse were adoptively transferred into strain-matched mice via tail vein injection. Control cells were from naive mice. After 24 hours, all recipient mice (n = 5-8 per group) were challenged with 1 IU FIX in adjuvant via subcutaneous injection. IgG titers against FIX (B) were determined 3 weeks later. (C) Purified CD4+CD25 cells were further divided into LAP+ and LAP cells via magnetic sorting. The cells were adoptively transferred (n = 4-6 per group), followed by immunization with FIX. IgG titers against FIX (D) were determined 3 weeks later. Control mice had received cells from naive mice. Data are average ± SEM. Shown are data from 2 independent experiments that showed similar results.

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