Author(s): Youngblood B, Oestreich KJ, Ha SJ, Duraiswamy J, Akondy RS, , Youngblood B, Oestreich KJ, Ha SJ, Duraiswamy J, Akondy RS, , Youngblood B, Oestreich KJ, Ha SJ, Duraiswamy J, Akondy RS, , Youngblood B, Oestreich KJ, Ha SJ, Duraiswamy J, Akondy RS,
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Abstract Functionally exhausted T cells have high expression of the PD-1 inhibitory receptor, and therapies that block PD-1 signaling show promise for resolving chronic viral infections and cancer. By using human and murine systems of acute and chronic viral infections, we analyzed epigenetic regulation of PD-1 expression during CD8(+) T cell differentiation. During acute infection, naive to effector CD8(+) T cell differentiation was accompanied by a transient loss of DNA methylation of the Pdcd1 locus that was directly coupled to the duration and strength of T cell receptor signaling. Further differentiation into functional memory cells coincided with Pdcd1 remethylation, providing an adapted program for regulation of PD-1 expression. In contrast, the Pdcd1 regulatory region was completely demethylated in exhausted CD8(+) T cells and remained unmethylated even when virus titers decreased. This lack of DNA remethylation leaves the Pdcd1 locus poised for rapid expression, potentially providing a signal for premature termination of antiviral functions. Copyright © 2011 Elsevier Inc. All rights reserved.
This article was published in Immunity
and referenced in Immunotherapy: Open Access