CD19 CAR-T cell therapy: a new dawn for autoimmune rheumatic diseases?
Metadatos
Mostrar el registro completo del ítemAutor
Rangel Peláez, Carlos; Martínez Gutiérrez, Laura; Tristán Manzano, María; Callejas Rubio, José Luis; Ortego Centeno, Norberto; Martín, Francisco; Martín, JavierEditorial
Frontiers Media
Fecha
2024-12-17Referencia bibliográfica
Rangel Rodríguez, C. et. al. Front. Immunol. 15:1502712. [https://doi.org/10.3389/fimmu.2024.1502712]
Patrocinador
Cooperative Research Networks Oriented to Health Results (RICORS), Inflammatory Diseases Network (REI) (RD21/ 0002/0039; RD24/0007/0016); Carlos III Health Institute (ISCIII); Next Generation EU funds, which finance the actions of the Recovery, Transformation and Resilience Plan. TerAv RD21/ 0017/0004 (FM); Grant PI21/00298 (FM) funded by Instituto de Salud Carlos III (ISCIII) from the Spanish Ministry of Science and Innovation, by the Instituto de Salud Carlos III (ISCIII) and the European Regional Development Fund (FEDER), by Consejería de Salud y Familias; Junta de Andalucía - FEDER/European Cohesion Fund (FSE) for Andalucía: Grants: PECART-0031-2020; Grant PREP2022-000747 funded by MICIU/AEI /10.13039/501100011033 and by ESF+Resumen
Autoimmune rheumatic diseases (ARDs), such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis, involve dysregulated immune responses causing chronic inflammation and tissue damage. Despite advancements in clinical management, many patients do not respond to current treatments, which often show limited efficacy due to the persistence of autoreactive B cells. Chimeric antigen receptor (CAR)-T cell therapy, which has shown success in oncology for B cell malignancies, targets specific antigens and involves the adoptive transfer of genetically engineered T cells. CD19 CAR-T cells, in particular, have shown promise in depleting circulating B cells and achieving clinical remission. This review discusses the potential of CD19 CAR-T cells in ARDs, highlighting clinical achievements and addressing key considerations such as optimal target cell populations, CAR construct design, acceptable toxicities, and the potential for lasting immune reset, crucial for the safe and effective adoption of CAR-T cell therapy in autoimmune treatments.