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B 细胞成熟抗原靶向 CAR-T 细胞治疗后的微小病变肾病

英文原题:Minimal Change Disease Following B-Cell Maturation Antigen-Directed Chimeric Antigen Receptor T-Cell Therapy.

查看英文原题

Minimal Change Disease Following B-Cell Maturation Antigen-Directed Chimeric Antigen Receptor T-Cell Therapy.

PubMed 2026/03/12(内容时间) Kidney Med Q1 · IF 4.1(JCR 2025)

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中文摘要

急性肾损伤(AKI)是嵌合抗原受体(CAR)T细胞治疗公认的并发症,通常归因于细胞因子释放综合征和急性肾小管损伤。然而,CAR-T 细胞治疗后的肾小球疾病较为罕见。我们报告一例微小病变肾病,表现为AKI和肾病范围蛋白尿,发生于一名复发难治性多发性骨髓瘤患者接受B细胞成熟抗原靶向CAR-T 细胞治疗ciltacabtagene autoleucel后3周。肾活检显示弥漫性足细胞足突消失,并以CD4+ T细胞为主,提示B细胞成熟抗原靶向CAR-T 细胞治疗可能存在靶向在靶、脱肿瘤效应,导致足细胞损伤。患者接受了一剂rituximab以及短程皮质类固醇治疗,至治疗第4周时肾功能完全恢复。本报告强调需要进一步研究CAR-T 细胞治疗后肾毒性的机制,以及在此背景下免疫抑制治疗的潜在获益与风险。

展开英文摘要原文

Acute kidney injury (AKI) is a well-recognized complication of chimeric antigen receptor (CAR) T-cell therapy, typically attributed to cytokine release syndrome and acute tubular injury.

However, glomerular disease post CAR-T cell is rare. We report a case of minimal change disease presenting with AKI and nephrotic-range proteinuria 3 weeks after B-cell maturation antigen-directed CAR-T cell therapy, ciltacabtagene autoleucel, in a patient with relapsed refractory multiple myeloma. The kidney biopsy revealed diffuse podocyte foot process effacement and a predominance of CD4+ T cells with potential on-target, off-tumor effect of B-cell maturation antigen-directed CAR-T cell therapy, leading to podocyte injury.

The patient received one dose of rituximab along with a short course of corticosteroid and had complete kidney recovery by week 4 of therapy. This report emphasizes the need for further investigation into the mechanism of kidney toxicity following CAR-T cell therapy, and potential benefits and risks of immunosuppressive therapy in this context.

论文信息

作者
Shivaraj K、Mamlouk O、Tchakarov A、Patel K、Abudayyeh A
单位
Division of Internal Medicine, Section of Nephrology, The University of Texas MD Anderson Cancer Center, Houston, TX.United States
文献类型
病例报告
期刊
Kidney medicine2026 May
原文标识
PubMed 42004656 · DOI 10.1016/j.xkme.2026.101326