← 返回

IFNγ 抑制在 CAR-T 细胞治疗相关难治性细胞因子释放综合征中的潜在作用

英文原题:Potential Role of IFNγ Inhibition in Refractory Cytokine Release Syndrome Associated with CAR T-cell Therapy.

查看英文原题

Potential Role of IFNγ Inhibition in Refractory Cytokine Release Syndrome Associated with CAR T-cell Therapy.

PubMed 2022/03/01(内容时间) Blood Cancer Discov Q1 · IF 12.2(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

本文综述免疫治疗继发细胞因子释放综合征(CRS)的病理生理机制和处理方法,并介绍对IL-6抑制和糖皮质激素治疗无反应的难治性CRS的潜在应对选择;目前尚无经证实有效的治疗方法。为说明这一问题,本文报告一名B细胞急性淋巴细胞白血病患者在接受CD19靶向CAR-T 细胞治疗后发生难治性4级CRS。患者接受托珠单抗、甲泼尼龙、siltuximab和IFN抑制剂emapalumab治疗,白血病完全缓解并持续12个月。Bailey等人的相关论文见第136页(15)。

展开英文摘要原文

Here we review the pathophysiology and management of cytokine release syndrome (CRS) secondary to immunotherapy, and potential options for CRS refractory to IL6 inhibition and glucocorticoids, for which there are no proven treatments.

To illustrate, we describe a patient with B-cell acute lymphoblastic leukemia who developed refractory grade 4 CRS following CD19-directed chimeric antigen receptor T-cell therapy, treated with tocilizumab, methylprednisolone, siltuximab, and the IFN inhibitor emapalumab, with complete remission from leukemia for 12 months. See related article by Bailey et al. , p. 136 (15).

论文信息

作者
McNerney KO、DiNofia AM、Teachey DT、Grupp SA、Maude SL
单位
Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.United States
文献类型
社论 · 美国 NIH 资助研究 · 非美国政府资助研究 · 评论
期刊
Blood cancer discovery2022 Mar 1
原文标识
PubMed 35015687 · DOI 10.1158/2643-3230.BCD-21-0203