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病例报告:CAR-T 细胞治疗受者治疗后发生活动性结核感染——回顾性病例系列

英文原题:Case Report: Active tuberculosis infection in CAR T-cell recipients post CAR T-cell therapy: a retrospective case series.

查看英文原题

Case Report: Active tuberculosis infection in CAR T-cell recipients post CAR T-cell therapy: a retrospective case series.

PubMed 2023/05/11(内容时间) Front Cell Infect Microbiol Q1 · IF 5.5(JCR 2025)

研究概要

我们的研究提供了首例CD19/CD22靶向CAR T细胞治疗后活动性TB的系列报告。

中文摘要

B细胞恶性肿瘤通过嵌合抗原受体(CAR)T细胞疗法已取得高缓解率。新近报道提示,新型免疫治疗肿瘤存在活动性结核(TB)风险。然而,CAR T细胞治疗后患者TB的研究有限。在本病例系列研究中,我们描述了五例在单独接受CD19/CD22靶向CAR T细胞治疗后或继自体干细胞移植(ASCT)后发生活动性TB的患者。其中一例患者在CAR T细胞治疗后30天内发生活动性TB,发热是主要表现症状;其他四例患者肺外表现常见,并在CAR T细胞治疗后30天后出现。五例患者中有四例经抗TB治疗后好转,但一例异烟肼耐药患者死于中枢神经系统TB感染。我们的研究提供了首例系列报告,描述CD19/CD22靶向CAR T细胞治疗后活动性TB。

展开英文摘要原文

High response rates in B-cell malignancies have been achieved with chimeric antigen receptor (CAR) T-cell therapy. Emerging reports indicate a risk of active tuberculosis (TB) with novel immunotherapy for tumors. However, studies of TB in patients post CAR T-cell therapy are limited. In this case series study, we describe five patients with active TB post CD19/CD22 target CAR T-cell therapy alone or following autologous stem cell transplantation (ASCT). One of the patients developed active TB within the first 30 days post CAR T-cell therapy, and fever was the dominant presenting symptom; extrapulmonary manifestations of active TB were common in the other four patients and manifested after the first 30 days of CAR T-cell therapy. Four of the five patients improved with anti-TB treatment, but one patient with isoniazid resistance died of central nervous system TB infection. Our study provides the first series report of active TB following CD19/CD22 target CAR T-cell therapy.

论文信息

作者
Zhang P、Huang L、Zheng M、Zhang C、Wan D、Wei J、Cao Y
单位
Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.China
文献类型
病例报告 · 非美国政府资助研究
期刊
Frontiers in cellular and infection microbiology2023
原文标识
PubMed 37249982 · DOI 10.3389/fcimb.2023.1147454