Advancements and challenges in CAR T cell therapy in autoimmune diseases.
Larissa Valor-MéndezFabian MüllerJule TaubmannAndreas MackensenWei WangRich A FurieRalf GoldAiden HaghikiaPeter A MerkelRoberto CaricchioMaria-Antonietta D'AgostinoFranco LocatelliCarl H JuneDimitrios MougiakakosPublished in: Nature reviews. Rheumatology (2024)
Chimeric antigen receptor (CAR) T cells are highly effective at targeting and eliminating cells of the B cell lineage. CAR T cell therapy has become a standard-of-care treatment for patients with relapsed or refractory B cell malignancies. In addition, the administration of genetically modified T cells with the capacity to deplete B cells and/or plasma cells has tremendous therapeutic potential in autoimmune diseases. In the past few years, CD19-based and B cell maturation antigen (BCMA)-based CAR T cell therapies have been applied to various B cell-mediated autoimmune diseases including systemic lupus erythematosus, idiopathic inflammatory myopathy, systemic sclerosis, neuromyelitis optica spectrum disorder, myasthenia gravis and multiple sclerosis. The scientific rationale behind this approach is that deep depletion of B cells, including autoreactive B cell clones, could restore normal immune function, referred to as an immune reset. In this Review, we discuss important aspects of CAR T cell therapy in autoimmune disease, including considerations relating to patient selection, safety, efficacy and medical management. These considerations are based on the early experiences of CAR T cell therapy in autoimmune diseases, and as the field of CAR T cell therapy in autoimmune diseases continues to rapidly evolve, these issues will remain subject to ongoing refinement and adaptation.
Keyphrases
- cell therapy
- systemic sclerosis
- multiple sclerosis
- induced apoptosis
- stem cells
- systemic lupus erythematosus
- mesenchymal stem cells
- myasthenia gravis
- healthcare
- cell cycle arrest
- interstitial lung disease
- spectrum disorder
- oxidative stress
- palliative care
- mental health
- clinical trial
- endoplasmic reticulum stress
- acute lymphoblastic leukemia
- cancer therapy
- late onset
- multiple myeloma
- bone marrow
- drug delivery
- early onset
- hodgkin lymphoma
- idiopathic pulmonary fibrosis
- nk cells