Open AccessEpigenetic scars of CD8+ T cell exhaustion persist after cure of chronic infection in humans
Author(s) -
Kathleen B. Yates,
Pierre Tonnerre,
Geneviève Martin,
Ulrike Gerdemann,
Rose Al Abosy,
Dawn E. Comstock,
Sarah A. Weiss,
David Wolski,
Damien C. Tully,
Raymond T. Chung,
Todd M. Allen,
Arthur Y. Kim,
Sarah Fidler,
Julie Fox,
John Frater,
Georg M. Lauer,
W. Nicholas Haining,
Debattama R. Sen
Publication year - 2021
Publication title -
nature immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.074
H-Index - 388
eISSN - 1529-2916
pISSN - 1529-2908
DOI - 10.1038/s41590-021-00979-1
Subject(s) - epigenetics , chromatin , biology , cytotoxic t cell , immunology , inflammation , cd8 , chronic infection , immune system , genetics , gene , in vitro
T cell exhaustion is an induced state of dysfunction that arises in response to chronic infection and cancer. Exhausted CD8 + T cells acquire a distinct epigenetic state, but it is not known whether that chromatin landscape is fixed or plastic following the resolution of a chronic infection. Here we show that the epigenetic state of exhaustion is largely irreversible, even after curative therapy. Analysis of chromatin accessibility in HCV- and HIV-specific responses identifies a core epigenetic program of exhaustion in CD8 + T cells, which undergoes only limited remodeling before and after resolution of infection. Moreover, canonical features of exhaustion, including super-enhancers near the genes TOX and HIF1A, remain 'epigenetically scarred.' T cell exhaustion is therefore a conserved epigenetic state that becomes fixed and persists independent of chronic antigen stimulation and inflammation. Therapeutic efforts to reverse T cell exhaustion may require new approaches that increase the epigenetic plasticity of exhausted T cells.