CAR T-cell therapy in autoimmune diseases

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 免疫疗法 T细胞 抗体 免疫系统
作者
Georg Schett,Andréas Mackensen,Andréas Mackensen
出处
期刊:The Lancet [Elsevier BV]
卷期号:402 (10416): 2034-2044 被引量:387
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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