1. Epigenetic regulators of clonal hematopoiesis control CD8 T cell stemness during immunotherapy.
- Author
-
Kang TG, Lan X, Mi T, Chen H, Alli S, Lim SE, Bhatara S, Vasandan AB, Ward G, Bentivegna S, Jang J, Spatz ML, Han JH, Schlotmann BC, Jespersen JS, Derenzo C, Vogel P, Yu J, Baylin S, Jones P, O'Connell C, Grønbæk K, Youngblood B, and Zebley CC
- Subjects
- Animals, Humans, Mice, B7-H1 Antigen metabolism, B7-H1 Antigen genetics, Cell Differentiation, DNA (Cytosine-5-)-Methyltransferases genetics, DNA (Cytosine-5-)-Methyltransferases metabolism, Histones metabolism, CD8-Positive T-Lymphocytes immunology, Clonal Hematopoiesis genetics, Dioxygenases genetics, DNA Methyltransferase 3A genetics, DNA-Binding Proteins genetics, Epigenesis, Genetic, Immune Checkpoint Inhibitors therapeutic use, Immunosuppression Therapy, Proto-Oncogene Proteins genetics, Repressor Proteins genetics, T-Cell Exhaustion genetics
- Abstract
Epigenetic reinforcement of T cell exhaustion is known to be a major barrier limiting T cell responses during immunotherapy. However, the core epigenetic regulators restricting antitumor immunity during prolonged antigen exposure are not clear. We investigated three commonly mutated epigenetic regulators that promote clonal hematopoiesis to determine whether they affect T cell stemness and response to checkpoint blockade immunotherapy. CD8 T cells lacking Dnmt3a, Tet2, or Asxl1 preserved a progenitor-exhausted (Tpex) population for more than 1 year during chronic antigen exposure without undergoing malignant transformation. Asxl1 controlled the self-renewal capacity of T cells and reduced CD8 T cell differentiation through H2AK119 ubiquitination and epigenetic modification of the polycomb group-repressive deubiquitinase pathway. Asxl1-deficient T cells synergized with anti-PD-L1 immunotherapy to improve tumor control in experimental models and conferred a survival advantage to mutated T cells from treated patients.
- Published
- 2024
- Full Text
- View/download PDF