TY - JOUR
T1 - Allogeneic CD19-targeted CAR-T therapy in refractory systemic lupus erythematosus achieved durable remission
AU - Wang, Dandan
AU - Wang, Xiaobing
AU - Tan, Binghe
AU - Wen, Xin
AU - Ye, Songying
AU - Wu, Yingyi
AU - Cao, Xuan
AU - Zhang, Xin
AU - Wang, Chun
AU - Geng, Linyu
AU - Zhang, Huayong
AU - Feng, Xuebing
AU - Zheng, Biao
AU - He, Yanran
AU - Liu, Mingyao
AU - Wu, Xin
AU - Du, Bing
AU - Sun, Lingyun
AU - Xu, Huji
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/10/10
Y1 - 2025/10/10
N2 - Background: Autoreactive B cells play a key role in the pathogenesis of systemic lupus erythematosus (SLE). The aim of this study is to assess the safety of allogeneic chimeric antigen receptor (CAR)-T cells for patients with lupus. This study was registered at ClinicalTrials.gov (NCT05859997). Methods: In this study, 3 patients with refractory and severe SLE with multi-organ involvement were enrolled. Genetically engineered healthy-donor-derived, CD19-targeting CAR-T cells were infused intravenously at a dose of 1 million cells per kilogram of body weight. The safety indices, including the occurrence of graft-versus-host disease (GvHD), cytokine release syndrome (CRS), and immune effector cell-associated neurotoxicity syndrome (ICANS), were evaluated. The proliferation of CAR+ T cells and the number of peripheral B cells were assessed. The clinical efficacy was also assessed based on the SELENA-SLEDAI, SLEDAI-2K, BILAG, clinical SLE responder index-4 (SRI-4), and DORIS remission index. Findings: Between August 2023 and October 2023, 3 patients with SLE were enrolled and completed a 12-month follow-up. No patient underwent GvHD, CRS, or ICANS, and no severe adverse events were recorded. CAR+ T cells expanded in vivo, peaking at day 14, and then declined. The percentage of B cells in lymphocytes and the absolute circulating B cell counts were profoundly decreased. Patient 1 withdrew from the study at month 1 due to unresolved and severe thrombocytopenia and the need for the addition of an immunosuppressive drug. SELENA-SLEDAI and SLEDAI-2K scores declined, and all the patients reached SRI-4 remission at the last visit. Conclusions: In patients with severe and refractory SLE, allogeneic CAR-T cell therapy showed profound safety and clinical efficacy for disease remission. Funding: 82320108010, 31821003, 81930043, 82330055, and U24A20380.
AB - Background: Autoreactive B cells play a key role in the pathogenesis of systemic lupus erythematosus (SLE). The aim of this study is to assess the safety of allogeneic chimeric antigen receptor (CAR)-T cells for patients with lupus. This study was registered at ClinicalTrials.gov (NCT05859997). Methods: In this study, 3 patients with refractory and severe SLE with multi-organ involvement were enrolled. Genetically engineered healthy-donor-derived, CD19-targeting CAR-T cells were infused intravenously at a dose of 1 million cells per kilogram of body weight. The safety indices, including the occurrence of graft-versus-host disease (GvHD), cytokine release syndrome (CRS), and immune effector cell-associated neurotoxicity syndrome (ICANS), were evaluated. The proliferation of CAR+ T cells and the number of peripheral B cells were assessed. The clinical efficacy was also assessed based on the SELENA-SLEDAI, SLEDAI-2K, BILAG, clinical SLE responder index-4 (SRI-4), and DORIS remission index. Findings: Between August 2023 and October 2023, 3 patients with SLE were enrolled and completed a 12-month follow-up. No patient underwent GvHD, CRS, or ICANS, and no severe adverse events were recorded. CAR+ T cells expanded in vivo, peaking at day 14, and then declined. The percentage of B cells in lymphocytes and the absolute circulating B cell counts were profoundly decreased. Patient 1 withdrew from the study at month 1 due to unresolved and severe thrombocytopenia and the need for the addition of an immunosuppressive drug. SELENA-SLEDAI and SLEDAI-2K scores declined, and all the patients reached SRI-4 remission at the last visit. Conclusions: In patients with severe and refractory SLE, allogeneic CAR-T cell therapy showed profound safety and clinical efficacy for disease remission. Funding: 82320108010, 31821003, 81930043, 82330055, and U24A20380.
KW - CAR-T cell
KW - Translation to patients
KW - allogeneic
KW - remission
KW - safety
KW - systemic lupus erythematosus
UR - https://www.scopus.com/pages/publications/105006980485
U2 - 10.1016/j.medj.2025.100749
DO - 10.1016/j.medj.2025.100749
M3 - 文章
AN - SCOPUS:105006980485
SN - 2666-6359
VL - 6
JO - Med
JF - Med
IS - 10
M1 - 100749
ER -