Facing CAR T Cell Challenges on the Deadliest Paediatric Brain Tumours.
Cristina Ferreras Bárbara PascualLucía FernándezLaura Clares-VillaMarta Ibáñez-NavarroCarla Martín-CortázarIsabel Esteban-RodríguezJavier SacedaPérez-Martínez AntonioPublished in: Cells (2021)
Central nervous system (CNS) tumours comprise 25% of the paediatric cancer diagnoses and are the leading cause of cancer-related death in children. Current treatments for paediatric CNS tumours are far from optimal and fail for those that relapsed or are refractory to treatment. Besides, long-term sequelae in the developing brain make it mandatory to find new innovative approaches. Chimeric antigen receptor T cell (CAR T) therapy has increased survival in patients with B-cell malignancies, but the intrinsic biological characteristics of CNS tumours hamper their success. The location, heterogeneous antigen expression, limited infiltration of T cells into the tumour, the selective trafficking provided by the blood-brain barrier, and the immunosuppressive tumour microenvironment have emerged as the main hurdles that need to be overcome for the success of CAR T cell therapy. In this review, we will focus mainly on the characteristics of the deadliest high-grade CNS paediatric tumours (medulloblastoma, ependymoma, and high-grade gliomas) and the potential of CAR T cell therapy to increase survival and patients' quality of life.
Keyphrases
- cell therapy
- high grade
- stem cells
- intensive care unit
- low grade
- blood brain barrier
- mesenchymal stem cells
- emergency department
- end stage renal disease
- white matter
- ejection fraction
- poor prognosis
- acute lymphoblastic leukemia
- chronic kidney disease
- resting state
- acute myeloid leukemia
- newly diagnosed
- prognostic factors
- papillary thyroid
- single cell
- bone marrow
- long non coding rna
- risk assessment
- peritoneal dialysis
- squamous cell
- childhood cancer
- patient reported