Th1 and Th2 cell fates are traditionally viewed as mutually exclusive, but recent work suggests that these lineages may be more plastic than previously thought. When isolating splenic CD4+ T cells from mice infected with the parasitic helminth Schistosoma mansoni, we observed a defined population of IFN-γ/IL-4 double-positive cells. These IFN-γ+IL-4+ cells showed differences in DNA methylation at the Ifng and Il4 loci when compared with IFN-γ+IL-4- (Th1) and IFN-γ-IL-4+ (Th2) cells, demonstrating that they represent a distinct effector cell population. IFN-γ+IL-4+ cells also displayed a discrete DNA methylation pattern at a CpG island within the body of the Gata3 gene, which encodes the master regulator of Th2 identity. DNA methylation at this region correlated with decreased Gata3 levels, suggesting a possible role in controlling Gata3 expression. These data provide important insight into the molecular mechanisms behind the co-existence of Th1 and Th2 characteristics. © 2014 The Authors. European Journal of Immunology published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
CITATION STYLE
Deaton, A. M., Cook, P. C., De Sousa, D., Phythian-Adams, A. T., Bird, A., & Macdonald, A. S. (2014). A unique DNA methylation signature defines a population of IFN-γ/IL-4 double-positive T cells during helminth infection. European Journal of Immunology, 44(6), 1835–1841. https://doi.org/10.1002/eji.201344098
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