Abstract
Abstract T cell exhaustion, a state of dysfunction occurring during chronic infections and cancer, is marked by a progressive loss of effector functions and increased expression of inhibitory receptors. In chronic infection, CD8 T cells differentiate into TCF1+ progenitor (TPRO), CX3CR1+ effector (TEFF), and terminally exhausted (TEXH) subsets. The differentiation pathways are governed by complex transcription factor (TF) networks. Employing regulon analysis enabled by single-cell RNA+ATAC multiome sequencing, we dissected the TF networks orchestrating the fate of exhausted CD8 T cell populations. Our integrative analysis, complemented by single-cell CRISPR screening, highlighted Krüppel-like factor 2 (KLF2) as a pivotal TF necessary for maintaining TPRO cells and generating TEFF cells. Our research also revealed that KLF2 regulates the distinct distribution patterns of CD8 T cell subsets across organs. More intriguingly, multiomic analysis uncovered a novel function of Klf2 in limiting T cell exhaustion. Klf2-deficient CD8 T cells exhibited a marked increase in exhaustion signature genes. ATAC-seq and CUT&TAG assays further revealed different chromatin accessibility and histone modifications within Klf2 and its enhancers across CD8 T cell subsets. These insights underscore the differential transcriptional and epigenetic regulation of Klf2, presenting a novel mechanism that influences the cell fate decision of CD8 T cells during chronic infections.
Published Version
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