MYB orchestrates T cell exhaustion and response to checkpoint inhibition
The University of Melbourne · Peter Doherty Institute · +7 more institutions
Abstract
Abstract CD8 + T cells that respond to chronic viral infections or cancer are characterized by the expression of inhibitory receptors such as programmed cell death protein 1 (PD-1) and by the impaired production of cytokines. This state of restrained functionality—which is referred to as T cell exhaustion 1,2 —is maintained by precursors of exhausted T (T PEX ) cells that express the transcription factor T cell factor 1 (TCF1), self-renew and give rise to TCF1 − exhausted effector T cells 3–6 . Here we show that the long-term proliferative potential, multipotency and repopulation capacity of exhausted T cells during chronic infection are selectively preserved in a small population of transcriptionally distinct…
Citation impact
- FWCI
- 18.23
- Percentile
- 100%
- References
- 63
Authors
22- CTCarlson TsuiCorresponding
The University of Melbourne, Peter Doherty Institute
- LKLorenz Kretschmer
Technical University of Munich
- SRSvenja Rapelius
Technical University of Munich
- SSSarah S. Gabriel
The University of Melbourne, Peter Doherty Institute
- DCDavid Chisanga
The University of Melbourne, Walter and Eliza Hall Institute of Medical Research, La Trobe University, Olivia Newton-John Cancer Wellness & Research Centre
Topics & keywords
- Cell biology
- Population
- Biology
- Transcription factor
- T cell
- CD8
- Immunology
- Cancer research
- Good health and well-being
Funding
- DFDeutsche ForschungsgemeinschaftAwards: SFB 1054, 452881907, SFB-TRR 338/1 2021-452881907, SFB-TRR 338/1, 338/1 2021-452881907, SFB-TRR 338, 210592381
- EKElse Kröner-Fresenius-Stiftung
- DKDeutsche KrebshilfeAwards: 70113918, DKH 70113918
- MRMedical Research Council
- NHNational Health and Medical Research Council