T cell senescence and CAR-T cell exhaustion in hematological malignancies.
Dimitri KasakovskiLing XuYangqiu LiPublished in: Journal of hematology & oncology (2018)
T cell senescence has been recognized to play an immunosuppressive role in the aging population and cancer patients. Strategies dedicated to preventing or reversing replicative and premature T cell senescence are required to increase the lifespan of human beings and to reduce the morbidity from cancer. In addition, overcoming the T cell terminal differentiation or senescence from lymphoma and leukemia patients is a promising approach to enhance the effectiveness of adoptive cellular immunotherapy (ACT). Chimeric antigen receptor T (CAR-T) cell and T cell receptor-engineered T (TCR-T) cell therapy highly rely on functionally active T cells. However, the mechanisms which drive T cell senescence remain unclear and controversial. In this review, we describe recent progress for restoration of T cell homeostasis from age-related senescence as well as recovery of T cell activation in hematological malignancies.
Keyphrases
- cell therapy
- endothelial cells
- dna damage
- stress induced
- stem cells
- randomized controlled trial
- mesenchymal stem cells
- ejection fraction
- systematic review
- newly diagnosed
- immune response
- acute myeloid leukemia
- young adults
- oxidative stress
- papillary thyroid
- chronic kidney disease
- regulatory t cells
- patient reported outcomes
- binding protein