Mechanisms of resistance to chimeric antigen receptor-T cells in haematological malignancies.
Marco RuellaFelix KorellPatrizia PorazziMarcela V MausPublished in: Nature reviews. Drug discovery (2023)
Chimeric antigen receptor (CAR)-T cells have recently emerged as a powerful therapeutic approach for the treatment of patients with chemotherapy-refractory or relapsed blood cancers, including acute lymphoblastic leukaemia, diffuse large B cell lymphoma, follicular lymphoma, mantle cell lymphoma and multiple myeloma. Nevertheless, resistance to CAR-T cell therapies occurs in most patients. In this Review, we summarize the resistance mechanisms to CAR-T cell immunotherapy by analysing CAR-T cell dysfunction, intrinsic tumour resistance and the immunosuppressive tumour microenvironment. We discuss current research strategies to overcome multiple resistance mechanisms, including optimization of the CAR design, improvement of in vivo T cell function and persistence, modulation of the immunosuppressive tumour microenvironment and synergistic combination strategies.
Keyphrases
- diffuse large b cell lymphoma
- multiple myeloma
- stem cells
- epstein barr virus
- end stage renal disease
- induced apoptosis
- oxidative stress
- liver failure
- ejection fraction
- newly diagnosed
- chronic kidney disease
- squamous cell carcinoma
- acute myeloid leukemia
- intensive care unit
- hepatitis b virus
- rectal cancer
- patient reported outcomes
- extracorporeal membrane oxygenation
- pi k akt