免疫学
医学
美罗华
嵌合抗原受体
B细胞
CD19
自身免疫
自身免疫性疾病
过继性细胞移植
抗原
细胞疗法
免疫疗法
T细胞
抗体
免疫系统
干细胞
生物
遗传学
作者
Georg Schett,Andréas Mackensen,Dimitrios Mougiakakos
出处
期刊:The Lancet
[Elsevier]
日期:2023-09-22
卷期号:402 (10416): 2034-2044
被引量:94
标识
DOI:10.1016/s0140-6736(23)01126-1
摘要
Despite the tremendous progress in the clinical management of autoimmune diseases, many patients do not respond to the currently used treatments. Autoreactive B cells play a key role in the pathogenesis of autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, and multiple sclerosis. B-cell-depleting monoclonal antibodies, such as rituximab, have poor therapeutic efficacy in autoimmune diseases, mainly due to the persistence of autoreactive B cells in lymphatic organs and inflamed tissues. The adoptive transfer of T cells engineered to target tumour cells via chimeric antigen receptors (CARs) has emerged as an effective treatment modality in B-cell malignancies. In the last 2 years treatment with autologous CAR T cells directed against the CD19 antigen has been introduced in therapy of autoimmune disease. CD19 CAR T cells induced a rapid and sustained depletion of circulating B cells, as well as in a complete clinical and serological remission of refractory systemic lupus erythematosus and dermatomyositis. In this paper, we discuss the evolving strategies for targeting autoreactive B cells via CAR T cells, which might be used for targeted therapy in autoimmune diseases.
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