Abstract
Exhausted CD8 T cells result from chronic antigen stimulation and have reduced ability to clear disease. The epigenetic regulation of the dysfunctional phenotype of exhausted CD8 T cells is a promising avenue for therapies aimed at reversing or preventing CD8 T cell exhaustion. Here, utilizing in vitro and in vivo models, we show global increase of the repressive histone modification H3K27me3 in CD8 T cell exhaustion and increased gene expression of the EZH2 form of the PRC2 complex, which is responsible for H3K27me3 deposition. H3K27me3 correlated with decreased gene expression and localized to naive/memory T cell genes in CD8 T cell exhaustion. PRC2 inhibition increased expression of the naive/memory genes while reducing expression of key exhaustion genes. Further, we identified potential enhancers and transcription factors predicted to promote expression of the PRC2 subunits. Our study highlights the importance of the repressive epigenetic landscape of exhausted CD8 T cells as well as a novel role for PRC2 in T cell biology.