TY - JOUR
T1 - CAR-T cell therapy for juvenile-onset autoimmune diseases
T2 - a promising future?
AU - for the C3I consortium
AU - Jouret, Maurine
AU - Viel, Sebastien
AU - Fournier, Benjamin
AU - Benezech, Sarah
AU - Avouac, Jérome
AU - Scherlinger, Marc
AU - Belot, Alexandre
AU - Peyrin-Biroulet, Laurent
AU - Jorgensen, Christian
AU - Meyer, Alain
AU - Forcade, Edouard
AU - Decroocq, Justine
AU - Pugnet, Grégory
AU - Bousso, Philippe
AU - Donnadieu, Emmanuel
AU - Mariette, Xavier
AU - Hermine, Olivier
AU - Amoura, Zahir
AU - Bitoun, Samuel
AU - Martin, Thierry
AU - Sibilia, Jean
AU - Cornec, Divi
AU - Choquet, Sylvain
AU - Jourde-Chiche, Noémie
AU - Richez, Christophe
AU - Bigenwald, Camille
AU - Terrier, Benjamin
AU - Launay, David
AU - Nocturne, Gaetane
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12/1
Y1 - 2025/12/1
N2 - Chimeric antigen receptor (CAR) T-cell therapy targeting B cells has shown promising results, including drug-free remission, in adult-onset autoimmune diseases. Extending this therapeutic approach to the pediatric population, particularly for juvenile autoimmune diseases, presents an exciting opportunity. However, challenges specific to juvenile-onset autoimmune conditions, such as long-term adverse events, heightened disease activity, and the imperative to reduce steroid exposure, must be considered. While this strategy appears viable for these severe conditions, the limited data available for this population and the absence of evidence on cases with a high genetic component, such as monogenic lupus, represent significant challenges. Most monogenic lupus cases are associated with innate immune defects, and the involvement of B cells in these genetic anomalies remains poorly understood. In this review, we examine the potential indications, current knowledge, and limitations of CAR-T cell therapy in juvenile-onset autoimmune diseases, extending the discussion beyond early-onset lupus.
AB - Chimeric antigen receptor (CAR) T-cell therapy targeting B cells has shown promising results, including drug-free remission, in adult-onset autoimmune diseases. Extending this therapeutic approach to the pediatric population, particularly for juvenile autoimmune diseases, presents an exciting opportunity. However, challenges specific to juvenile-onset autoimmune conditions, such as long-term adverse events, heightened disease activity, and the imperative to reduce steroid exposure, must be considered. While this strategy appears viable for these severe conditions, the limited data available for this population and the absence of evidence on cases with a high genetic component, such as monogenic lupus, represent significant challenges. Most monogenic lupus cases are associated with innate immune defects, and the involvement of B cells in these genetic anomalies remains poorly understood. In this review, we examine the potential indications, current knowledge, and limitations of CAR-T cell therapy in juvenile-onset autoimmune diseases, extending the discussion beyond early-onset lupus.
KW - Autoimmunity
KW - B cells
KW - CAR-T cells
KW - CD19
KW - Children
KW - Juvenile dermatomyositis
KW - Lupus
KW - Monogenic lupus
UR - http://www.scopus.com/inward/record.url?scp=105004919231&partnerID=8YFLogxK
U2 - 10.1186/s13075-025-03564-1
DO - 10.1186/s13075-025-03564-1
M3 - Comment/debate
AN - SCOPUS:105004919231
SN - 1478-6354
VL - 27
JO - Arthritis Research and Therapy
JF - Arthritis Research and Therapy
IS - 1
M1 - 102
ER -