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接受嵌合抗原受体(CAR)T细胞治疗的自身免疫性疾病患者的局部免疫效应细胞相关毒性综合征:一项观察性研究。

Local immune effector cell-associated toxicity syndrome in CAR T-cell treated patients with autoimmune disease: an observational study.

作者信息

Hagen Melanie, Müller Fabian, Wirsching Andreas, Kharboutli Soraya, Spoerl Silvia, Düsing Christina, Krickau Tobias, Metzler Markus, Völkl Simon, Aigner Michael, Kretschmann Sascha, Vasova Ingrid, Saake Marc, Schliep Stefan, Kubacki Torsten, Hunzelmann Nicolas, Bucci Laura, Taubmann Jule, Bergmann Christina, Györfi Andrea-Hermina, Dietrich Sascha, Distler Jörg H W, Grieshaber-Bouyer Ricardo, Mackensen Andreas, Schett Georg

机构信息

Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany; Deutsches Zentrum Immuntherapie (DZI), FAU Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Deutsches Zentrum Immuntherapie (DZI), FAU Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany; Department of Internal Medicine 5 - Hematology and Oncology, FAU Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

出版信息

Lancet Rheumatol. 2025 Jun;7(6):e424-e433. doi: 10.1016/S2665-9913(25)00091-8. Epub 2025 Apr 30.

DOI:10.1016/S2665-9913(25)00091-8
PMID:40318690
Abstract

BACKGROUND

CD19-targeting chimeric antigen receptor (CAR) T-cell therapy has advanced treatment strategies for severe autoimmune diseases such as systemic lupus erythematosus (SLE), systemic sclerosis, and idiopathic inflammatory myopathy. Data regarding side-effects are mostly generated from patients with malignancies, but little is known about autoimmune disease-specific adverse events. This study aimed to describe autoimmune disease-specific adverse events that occur with CAR T-cell therapy.

METHODS

In this observational study, patients of any age with autoimmune disease receiving CD19-targeting CAR T-cell therapy in two centres in Germany with a follow-up of at least 30 days were assessed for local organ-specific reactions occurring after CAR T-cell infusion. Observed reactions were documented according to localisation, time of onset, and duration, and were graded for severity (grade 1: spontaneous resolution; grade 2: glucocorticoid treatment due to symptoms lasting >1 week or presence of relevant inner organ involvement; grade 3: prolonged or new hospitalisation; grade 4: intensive care treatment). People with related lived experience were involved in the study design and implementation.

FINDINGS

Between March 1, 2021, and Oct 31, 2024, 39 patients with autoimmune disease were treated with CD19-targeting CAR T cells (20 with SLE, 13 with systemic sclerosis, six with idiopathic inflammatory myopathy). 25 (64%) patients were female and 14 (36%) were male. Median age was 36 years (IQR 22-44). 54 local reactions, which we termed local immune effector cell-associated toxicity syndrome (LICATS), were recorded, affecting 30 (77%) patients with a median time of onset of 10 days (IQR 9-21) from CAR T-cell infusion and a median duration of 11 days (5-14). LICATS exclusively occurred during the B-cell aplasia phase and only involved organs previously affected by the respective autoimmune disease. The most frequently affected organs were the skin (19 [35%] of 54) and the kidneys (12 [22%]). Most cases of LICATS were mild (grade 1: 35 [65%]; grade 2: 16 [30%]). Only three cases were grade 3. All events of LICATS resolved without sequelae.

INTERPRETATION

LICATS is a new form of toxicity in patients with autoimmune disease receiving CD19-targeting CAR T-cell therapy, most likely based on the cleansing of immune cells from the affected organs. It is self-limited, organ-specific, and usually mild in its intensity.

FUNDING

Deutsche Forschungsgemeinschaft (DFG), German Cancer Aid, Bundesministerium für Bildung und Forschung, European Union, Staedtler Foundation, Lupus Research Alliance, and donations from the Bendel family and the Bleyl family.

摘要

背景

靶向CD19的嵌合抗原受体(CAR)T细胞疗法推动了系统性红斑狼疮(SLE)、系统性硬化症和特发性炎性肌病等严重自身免疫性疾病治疗策略的发展。关于副作用的数据大多来自恶性肿瘤患者,但对于自身免疫性疾病特异性不良事件知之甚少。本研究旨在描述接受CAR T细胞疗法时发生的自身免疫性疾病特异性不良事件。

方法

在这项观察性研究中,对德国两个中心接受靶向CD19的CAR T细胞疗法且随访至少30天的任何年龄的自身免疫性疾病患者,评估CAR T细胞输注后发生的局部器官特异性反应。观察到的反应根据部位、发病时间和持续时间进行记录,并对严重程度进行分级(1级:自行缓解;2级:因症状持续>1周或存在相关内脏器官受累而接受糖皮质激素治疗;3级:延长住院时间或再次住院;4级:重症监护治疗)。有相关生活经历的人参与了研究设计和实施。

结果

在2021年3月1日至2024年10月31日期间,39例自身免疫性疾病患者接受了靶向CD19的CAR T细胞治疗(20例SLE患者,13例系统性硬化症患者,6例特发性炎性肌病患者)。25例(64%)为女性,14例(36%)为男性。中位年龄为36岁(四分位间距22 - 44岁)。记录到54例局部反应,我们将其称为局部免疫效应细胞相关毒性综合征(LICATS),30例(77%)患者受到影响,从CAR T细胞输注开始,中位发病时间为10天(四分位间距9 - 21天),中位持续时间为11天(5 - 14天)。LICATS仅发生在B细胞发育不全阶段,且仅累及先前受相应自身免疫性疾病影响的器官。最常受累的器官是皮肤(54例中的19例[35%])和肾脏(12例[22%])。大多数LICATS病例为轻度(1级:35例[65%];2级:16例[30%])。只有3例为3级。所有LICATS事件均无后遗症地得到缓解。

解读

LICATS是接受靶向CD19的CAR T细胞疗法的自身免疫性疾病患者的一种新的毒性形式,很可能是由于对受影响器官中的免疫细胞进行清除所致。它是自限性的、器官特异性的,且强度通常较轻。

资助

德国研究基金会(DFG)、德国癌症援助组织、联邦教育与研究部、欧盟、施泰德特勒基金会、狼疮研究联盟以及本德尔家族和布莱尔家族的捐赠。

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