TSHR-based chimeric antigen receptor T cell specifically deplete auto-reactive B lymphocytes for treatment of autoimmune thyroid disease

被引:5
|
作者
Duan, Honghong [1 ]
Jiang, Zhengrong [2 ]
Chen, Lijun [2 ]
Bai, Xuefeng [2 ]
Cai, Huiyao [2 ]
Yang, Xinna [2 ]
Huang, Huibin [2 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 2, Dept Obstet & Gynecol, Quanzhou 362000, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 2, Dept Endocrinol, Quanzhou 362000, Fujian, Peoples R China
关键词
Graves's disease; Autoimmune disease; TSHR; TRAb; GRAVES-DISEASE; LH/CGR CHIMERA; RECURRENCE; THERAPY; PATIENT; MODEL; TSAB;
D O I
10.1016/j.intimp.2023.110873
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Graves' disease (GD) is a prominent antibody-mediated autoimmune disorder characterized by stimulating an-tibodies (TRAb) that target the thyroid-stimulating hormone receptor (TSHR). Targeting and eliminating TRAb-producing B lymphocytes hold substantial therapeutic potential for GD. In this study, we engineered a novel chimeric antigen receptor T cell (CAR-T) therapy termed TSHR-CAR-T. This CAR-T construct incorporates the extracellular domain of the TSH receptor fused with the CD8 transmembrane and intracellular signal domain (4-1BB). TSHR-CAR-T cells demonstrated the ability to recognize and effectively eliminate TRAb-producing B lymphocytes both in vitro and in vivo. Leveraging this autoantigen-based chimeric receptor, our findings suggest that TSHR-CAR-T cells offer a promising and innovative immunotherapeutic approach for the treatment of antibody-mediated autoimmune diseases, including GD.
引用
收藏
页数:9
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