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嵌合抗原受体T细胞疗法后的血栓性微血管病

Thrombotic microangiopathy following chimeric antigen receptor T-cell therapy.

作者信息

Wu Matthew S, Koirala Abbal

机构信息

Department of Medicine, and.

Section of Nephrology, Department of Medicine, University of Washington Medical Center, Seattle, WA, USA.

出版信息

Clin Nephrol Case Stud. 2023 Feb 16;11:17-21. doi: 10.5414/CNCS111045. eCollection 2023.

Abstract

INTRODUCTION

Thrombotic microangiopathy (TMA) is characterized by microangiopathic hemolytic anemia and is associated with a variety of conditions and following hematopoietic stem cell transplantation. Chimeric antigen receptor T-cell (CAR-T) therapy is a novel immunotherapeutic approach using genetically modified autologous T cells. CAR-T therapy has been linked with injuries to vascular endothelium, but a direct association between CAR-T and TMA has not been reported.

CASE REPORTS

Two cases of TMAs following CAR-T treatment are reported here. In each case, clinical evidence of kidney injury, thrombocytopenia, and hemolytic anemia became apparent 2 - 3 months following CAR-T infusion. We describe the clinical course, management, and outcome of these experiences.

DISCUSSION/CONCLUSION: CAR-T cell therapy-associated TMA (CAR-T TMA) appear to be an entity that shares overlapping clinical features with transplant-associated TMA (TA-TMA). Based on our preliminary clinical observations, we discuss the best clinical diagnosis/classification criteria, underlying pathophysiology, and the implication of the apparently self-limiting course. With increasing use of CAR-T cell treatment in hematologic malignancies, systematic studies will be necessary to improve management of CAR-T TMA.

摘要

引言

血栓性微血管病(TMA)的特征为微血管病性溶血性贫血,与多种病症以及造血干细胞移植后相关。嵌合抗原受体T细胞(CAR-T)疗法是一种使用基因改造的自体T细胞的新型免疫治疗方法。CAR-T疗法与血管内皮损伤有关,但尚未有CAR-T与TMA之间存在直接关联的报道。

病例报告

本文报告了两例CAR-T治疗后发生TMA的病例。在每例病例中,肾损伤、血小板减少和溶血性贫血的临床证据在CAR-T输注后2至3个月变得明显。我们描述了这些病例的临床过程、管理及结果。

讨论/结论:CAR-T细胞疗法相关的TMA(CAR-T TMA)似乎是一种与移植相关的TMA(TA-TMA)具有重叠临床特征的实体。基于我们初步的临床观察,我们讨论了最佳的临床诊断/分类标准、潜在病理生理学以及明显的自限性病程的意义。随着CAR-T细胞治疗在血液系统恶性肿瘤中的使用增加,有必要进行系统性研究以改善对CAR-T TMA的管理。

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