TY - JOUR
T1 - CAR T-cell therapy in autoimmune diseases
T2 - where are we and where are we going?
AU - Club for Innovative Immunotherapies in Immune-mediated Inflammatory diseases (C3I)
AU - Scherlinger, Marc
AU - Nocturne, Gaetane
AU - Radic, Marko
AU - Launay, David
AU - Richez, Christophe
AU - Bousso, Philippe
AU - Forcade, Edouard
AU - Meyer, Alain
AU - Jorgensen, Christian
AU - Bigenwald, Camille
AU - Cornec, Divi
AU - Sibilia, Jean
AU - Choquet, Sylvain
AU - Martin, Thierry
AU - Belot, Alexandre
AU - Jouret, Maurine
AU - Bitoun, Samuel
AU - Amoura, Zahir
AU - Hermine, Olivier
AU - Mariette, Xavier
AU - Donnadieu, Emmanuel
AU - Avouac, Jérome
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Chimeric antigen receptor (CAR)-based therapies developed for the treatment of haematological malignancies have recently been repurposed to treat refractory systemic autoimmune diseases. In this Review we critically discuss the current data available on the use of CAR-based therapy in systemic autoimmune diseases, the current challenges, and the potential next steps toward their implementation into clinical practice. Beyond the targeting of B cells via CD19, we discuss the advantages and potential pitfalls of targeting plasma cells (B-cell Maturation Antigen or CD138) and other non-immune targets, such as fibroblast activated protein, and of aiming to restore immune homeostasis using CAR T regulatory cells. Crucial points need to be addressed for CAR-based therapy to become a viable treatment option for patients with systemic autoimmune diseases.
AB - Chimeric antigen receptor (CAR)-based therapies developed for the treatment of haematological malignancies have recently been repurposed to treat refractory systemic autoimmune diseases. In this Review we critically discuss the current data available on the use of CAR-based therapy in systemic autoimmune diseases, the current challenges, and the potential next steps toward their implementation into clinical practice. Beyond the targeting of B cells via CD19, we discuss the advantages and potential pitfalls of targeting plasma cells (B-cell Maturation Antigen or CD138) and other non-immune targets, such as fibroblast activated protein, and of aiming to restore immune homeostasis using CAR T regulatory cells. Crucial points need to be addressed for CAR-based therapy to become a viable treatment option for patients with systemic autoimmune diseases.
UR - http://www.scopus.com/inward/record.url?scp=105001524292&partnerID=8YFLogxK
U2 - 10.1016/S2665-9913(24)00377-1
DO - 10.1016/S2665-9913(24)00377-1
M3 - Review article
AN - SCOPUS:105001524292
SN - 2665-9913
JO - The Lancet Rheumatology
JF - The Lancet Rheumatology
ER -