Thymic dendritic cell-derived IL-27p28 promotes the establishment of functional bias against IFN-γ production in newly generated CD4 T cells through STAT1-related epigenetic mechanisms.

The newly generated CD4 single-positive (SP) T lymphocytes are featured by enhanced IL-4 but repressed IFN-γ production. The mechanisms underlying this functional bias remain elusive. Previous studies have reported that CD4 T cells from mice harboring dendritic cell (DC)-specific deletion of IL-27p28 display an increased capacity of IFN-γ production upon TCR stimulation. Here, we demonstrated that similarly altered functionality occurred in CD4SP thymocytes, recent thymic emigrants (RTEs), as well as naive T cells from either mice or mice deficient in the α subunit of IL-27 receptor. Therefore, DC-derived IL-27p28-triggered, IL-27Rα-mediated signal is critically involved in the establishment of functional bias against IFN-γ production during their development in the thymus. Epigenetic analyses indicated reduced DNA methylation of the locus and increased trimethylation of H3K4 at both and loci in CD4SP thymocytes from mice. Transcriptome profiling demonstrated that ablation resulted in the coordinated up-regulation of STAT1-activated genes. Concurrently, STAT1 was found to be constitutively activated. Moreover, we observed increased accumulation of STAT1 at the and loci and a strong correlation between STAT1 binding and H3K4me3 modification of these loci. Of note, deficiency exacerbated the autoimmune phenotype of mice. Collectively, this study reveals a novel mechanism underlying the functional bias of newly generated CD4 T cells and the potential relevance of such a bias in autoimmunity.