医学
系统性红斑狼疮
背景(考古学)
免疫学
自身免疫
嵌合抗原受体
微嵌合体
自身抗体
免疫疗法
抗体
疾病
免疫系统
内科学
怀孕
古生物学
胎儿
遗传学
生物
作者
Aurélien Guffroy,Léa Jacquel,Blandine Guffroy,Thierry Martin
出处
期刊:Joint Bone Spine
[Elsevier BV]
日期:2024-02-07
卷期号:91 (5): 105702-105702
被引量:4
标识
DOI:10.1016/j.jbspin.2024.105702
摘要
Chimeric Antigen Receptor T-cell therapy (CAR-T), currently employed routinely for treating B-cell malignancies, has emerged as a groundbreaking approach in addressing severe autoimmune diseases, especially for systemic lupus erythematosus (SLE). The immunological rationale for targeting B lymphocytes in autoimmune diseases is well-established, demonstrating success in numerous autoantibody-mediated autoimmune conditions through targeted therapies over several years. However, this approach has often proven ineffective in the context of systemic lupus erythematosus. Recent data on CAR-T usage in lupus, revealed promising results including rapid and prolonged remission without treatment, highlighting the potential of CAR-T therapy in severe lupus cases. This article provides a comprehensive overview of CAR-T cells, tracing their evolution from hematological malignancies to their recent applications in autoimmune disorder, especially in lupus. Clinical trials within a regulated framework are now imperative to assess the procedural aspects in order to validate the considerable promise of CAR-T cell therapy in the field of autoimmune diseases. This includes evaluating safety and long-term efficacy and security of the procedure, the benefit-risk ratio in the field of autoimmunity, the availability and cost-related issues associated with this emerging cellular therapy procedure.
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