Chen Dong's group report"BCL6 promotes a stem-like CD8+T cell program in cancer via antagonizing BLIMP1"

Abstract

Overcoming CD8⁺ T cell exhaustion is critical in cancer immunotherapy. Recently, an intratumor stem/progenitor-like CD8⁺ T cell (T_prog cell) population that mediates the persistence of antitumor responses has been defined, which can further develop into a terminally differentiated CD8⁺ T cell (T_term cell) subpopulation with potent cytotoxic functions. T_prog cells are the main responders to immune checkpoint blockade therapies, yet how extrinsic signals via transcription factors control T_prog cell generation and persistence in tumors is unclear. Here, we found that BCL6 inhibits tumor-specific T_term cell generation from T_prog cell downstream of TCF1. We show that Bcl6 deficiency reduced the persistence of T_prog cells, without affecting their generation, thus abrogating long-term tumor control. High-level BCL6 expression was observed in tumor-specific T cells in draining lymph nodes (LNs) and was associated with T cell exhaustion. This was observed in TOX⁺TCF1⁺ T_prog cells in both LNs and tumors. BCL6 expression in CD8⁺ T cells was up-regulated by TGF-β–SMAD2 signaling but down-regulated by the IL-2–STAT5 pathway. Mechanistically, BCL6 transcriptionally repressed the expression of T_term cell–associated genes and induced those of T_prog cell–related genes, in a manner antagonistic to BLIMP1. Prdm1 deficiency also promoted the T_prog cell program and greatly improved the efficacy of anti–PD-1 therapy. Thus, we identified the TGF-β–BCL6 and IL-2–BLIMP1 antagonistic pathways in regulation of antitumor CD8⁺ T cells, which may benefit the development of long-lasting and effective cancer immunotherapy.

Link: https://www.science.org/doi/10.1126/sciimmunol.adh1306