B细胞
B细胞受体
CD19
嵌合抗原受体
幼稚B细胞
免疫学
癌症研究
生物
抗原
免疫系统
细胞毒性T细胞
B-1电池
T细胞
抗体
自身抗体
断点群集区域
细胞因子
B细胞激活因子
受体
化学
分子生物学
细胞
B细胞淋巴瘤
细胞因子释放综合征
免疫球蛋白G
调节性B细胞
Fc受体
免疫突触
细胞毒性
免疫疗法
医学
作者
Ivan Cohen,Audrey Bochi-Layec,Jean Lemoine,Scott A. Jenks,Pedram Bayat,Ki Hyun Kim,Huiwu Zhao,Ositadimma Ugwuanyi,Federico Stella,Guido Ghilardi,Giulia Gabrielli,Sarah McCuaig,Anastasia Iatrou,Elisavet Vlachonikola,Maria Karipidou,Eleni Bouziani,David Espie,Ranjani Ramasubramanian,Andreas Agathangelidis,Aditya Bhosale
标识
DOI:10.1126/scitranslmed.adr9382
摘要
Current US Food and Drug Administration–approved chimeric antigen receptor (CAR) T cell therapies for B cell leukemias and lymphomas target CD19, which is widely expressed across the B cell lineage, often leading to on-target, off-tumor B cell depletion, prolonged immune suppression, and antigen-negative escape in a subset of patients. In contrast, B cell receptor (BcR) signaling is essential for the survival of most mature B cell neoplasms, and BcRs carrying the immunoglobulin heavy variable gene IGHV4-34 are highly enriched in B cell malignancies compared with normal B cells. Further, self-reactive IGHV4-34 + serum autoantibodies are enriched in aggressive systemic lupus erythematosus (SLE) and other autoimmune diseases. Here, we developed CAR T cells targeting the BcR carrying IGHV4-34 (CART4-34). We found that CART4-34 showed specific cytotoxicity and cytokine secretion toward IGHV4-34 + malignant B cells. In addition, although CD19 was down-regulated upon relapse after treatment with CART19, IGHV4-34 + BcR levels remained intact upon relapse after treatment with CART4-34, suggesting reduced risk of antigen-negative escape. In IGHV4-34 + HBL1 cell line–derived xenograft mouse models, CART4-34 showed robust expansion and antitumor activity comparable to those of CART19. Optimized CAR:BcR binding using shorter CAR hinge domains improved immune synapse morphology and in vivo activity. In addition, we showed that CART4-34 could target human IGHV4-34 + SLE B cells and deplete IGHV4-34 + autoantibodies ex vivo, without targeting healthy B cells or affecting total IgG titers. In conclusion, we developed a CAR T cell product that specifically targets pathogenic B cells in lymphoid malignancies and SLE, offering potential for precision cell therapy for these indications.
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