自身免疫性疾病中的 CD19 CAR T 细胞疗法--随访病例系列

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL New England Journal of Medicine Pub Date : 2024-02-22 DOI:10.1056/nejmoa2308917
Fabian Müller, Jule Taubmann, Laura Bucci, Artur Wilhelm, Christina Bergmann, Simon Völkl, Michael Aigner, Tobias Rothe, Ioanna Minopoulou, Carlo Tur, Johannes Knitza, Soraya Kharboutli, Sascha Kretschmann, Ingrid Vasova, Silvia Spoerl, Hannah Reimann, Luis Munoz, Roman G. Gerlach, Simon Schäfer, Ricardo Grieshaber-Bouyer, Anne-Sophie Korganow, Dominique Farge-Bancel, Dimitrios Mougiakakos, Aline Bozec, Thomas Winkler, Gerhard Krönke, Andreas Mackensen, Georg Schett
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引用次数: 0

摘要

背景治疗系统性红斑狼疮(SLE)、特发性炎症性肌炎和系统性硬化症等自身免疫性疾病通常需要长期的免疫抑制。我们评估了 15 名重症系统性红斑狼疮(8 名)、特发性炎症性肌炎(3 名)或系统性硬化症(4 名)患者,他们在接受氟达拉滨和环磷酰胺预处理后,接受了 CD19 嵌合抗原受体(CAR)T 细胞的单次输注。通过系统性红斑狼疮缓解定义(DORIS)缓解标准、美国风湿病学会-欧洲抗风湿联盟(ACR-EULAR)主要临床反应、欧洲硬皮病试验与研究组(EUSTAR)活动指数评分(分数越高表示疾病活动性越强)等指标,评估了CAR T细胞输注后两年内的疗效。结果中位随访时间为15个月(4至29个月)。B细胞增生的平均(±SD)持续时间为112±47天。所有系统性红斑狼疮患者都获得了DORIS缓解,所有特发性炎症性肌炎患者都获得了ACR-EULAR主要临床反应,所有系统性硬化症患者的EUSTAR活动指数得分都有所下降。所有患者都完全停止了免疫抑制治疗。10名患者出现了1级细胞因子释放综合征。结论在这一系列病例中,CD19 CAR T细胞转移似乎对三种不同的自身免疫性疾病都是可行、安全和有效的,这为进一步的对照临床试验提供了依据。(由德国科学基金会等资助)。
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CD19 CAR T-Cell Therapy in Autoimmune Disease — A Case Series with Follow-up

Background

Treatment for autoimmune diseases such as systemic lupus erythematosus (SLE), idiopathic inflammatory myositis, and systemic sclerosis often involves long-term immune suppression. Resetting aberrant autoimmunity in these diseases through deep depletion of B cells is a potential strategy for achieving sustained drug-free remission.

Methods

We evaluated 15 patients with severe SLE (8 patients), idiopathic inflammatory myositis (3 patients), or systemic sclerosis (4 patients) who received a single infusion of CD19 chimeric antigen receptor (CAR) T cells after preconditioning with fludarabine and cyclophosphamide. Efficacy up to 2 years after CAR T-cell infusion was assessed by means of Definition of Remission in SLE (DORIS) remission criteria, American College of Rheumatology–European League against Rheumatism (ACR–EULAR) major clinical response, and the score on the European Scleroderma Trials and Research Group (EUSTAR) activity index (with higher scores indicating greater disease activity), among others. Safety variables, including cytokine release syndrome and infections, were recorded.

Results

The median follow-up was 15 months (range, 4 to 29). The mean (±SD) duration of B-cell aplasia was 112±47 days. All the patients with SLE had DORIS remission, all the patients with idiopathic inflammatory myositis had an ACR–EULAR major clinical response, and all the patients with systemic sclerosis had a decrease in the score on the EUSTAR activity index. Immunosuppressive therapy was completely stopped in all the patients. Grade 1 cytokine release syndrome occurred in 10 patients. One patient each had grade 2 cytokine release syndrome, grade 1 immune effector cell–associated neurotoxicity syndrome, and pneumonia that resulted in hospitalization.

Conclusions

In this case series, CD19 CAR T-cell transfer appeared to be feasible, safe, and efficacious in three different autoimmune diseases, providing rationale for further controlled clinical trials. (Funded by Deutsche Forschungsgemeinschaft and others.)

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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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