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Systematic Review of Chimeric Antigen Receptor T-cell Therapy in Autoimmune Diseases

医学 不利影响 重症肌无力 嵌合抗原受体 梅德林 内科学 疾病 系统回顾 红斑狼疮 免疫学 自身免疫性疾病 临床实习 临床试验 细胞因子释放综合征 免疫疗法 系统性红斑狼疮 抗原 临床研究 肿瘤科 细胞因子 痹症科
作者
Nicole Hershkowitz,Anna Andrzejczyk,Vincent DeStefano,Michael W. Schuster,Qingping Yao
出处
期刊:Jcr-journal of Clinical Rheumatology [Lippincott Williams & Wilkins]
卷期号:32 (5): e173-e181 被引量:2
标识
DOI:10.1097/rhu.0000000000002354
摘要

OBJECTIVES: This study aimed to systematically summarize available clinical data on the use of chimeric antigen receptor (CAR) T-cell therapy in autoimmune diseases (ADs). METHODS: A systematic review was conducted using PubMed and other literature databases to identify publications on CAR-T therapy in ADs published since 2020. Eligible studies included single-case reports and case series from clinical trials, while studies involving duplicated patient populations were excluded in accordance with PRISMA guidelines. Extractable patient-level data were analyzed for key clinical outcomes. RESULTS: A total of 32 studies encompassing 124 patients with ADs who received CAR-T therapy were included. The primary diseases treated were systemic lupus erythematosus (SLE) and myasthenia gravis (MG), with smaller numbers of patients reported in other ADs. In SLE trials, 83% achieved clinical remission or low disease activity following CAR-T therapy, within the first few months following infusion. In MG trials, minimal symptom expression was achieved in 73%. CAR-T disappearance and B-cell reconstitution generally occurred within the first few months following infusion and were predominantly of a naïve phenotype. Mild cytokine release syndrome was the most common adverse event; serious adverse events were reported in 4.8% of patients without treatment-related deaths. CONCLUSION: Preliminary clinical evidence suggests that CAR-T therapy is associated with meaningful clinical response in selected ADs. Larger studies with standardized outcome measures and longer follow-up are needed to better define its safety and efficacy.
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