Directly Isolated Allogeneic Virus-Specific T Cells in Progressive Multifocal Leukoencephalopathy.

IF 20.4 1区 医学 Q1 CLINICAL NEUROLOGY JAMA neurology Pub Date : 2024-10-07 DOI:10.1001/jamaneurol.2024.3324
Nora Möhn, Lea Grote-Levi, Mike P Wattjes, Agnes Bonifacius, Dennis Holzwart, Franziska Hopfner, Sandra Nay, Sabine Tischer-Zimmermann, Mieke Luise Saßmann, Philipp Schwenkenbecher, Kurt-Wolfram Sühs, Nima Mahmoudi, Clemens Warnke, Julian Zimmermann, David Hagin, Lilia Goudeva, Rainer Blasczyk, Armin Koch, Britta Maecker-Kolhoff, Britta Eiz-Vesper, Günter Höglinger, Thomas Skripuletz
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Abstract

Importance: Progressive multifocal leukoencephalopathy (PML) is a life-threatening viral infection with no approved antiviral treatment.

Objective: To determine whether restoring the compromised immune system of patients with PML with directly isolated allogeneic virus-specific (DIAVIS) T cells is a promising therapeutic strategy, especially if other curative options are absent.

Design, setting, and participants: A retrospective case series of patients with PML who were treated with DIAVIS T cells was conducted between March 2020 and February 2022. T cells were isolated from healthy donors within 24 hours and targeted against the BK polyomavirus. Patients with PML were treated monocentrically. Eligibility for treatment with DIAVIS T cells was assessed for patients with confirmed PML, and exclusion criteria included stable PML disease and previous treatment with natalizumab.

Exposure: Fresh DIAVIS T cells were administered with a maximum dose of 2 × 104 CD3+ cells/kg body weight. Remaining T cells were cryopreserved in divided doses and administered in additional treatments approximately 2 and 6 weeks later.

Main outcomes and measures: Primary outcome measures were clinical response and survival of patients, compared with the outcomes of a historical reference group of PML cases receiving best supportive treatment (BST) and with recently published real-world data of patients with PML who were treated with immune checkpoint inhibition.

Results: The study cohort consisted of 28 patients (median [IQR] age, 60 [51-72] years; 20 male [71.4%]). Twenty-two patients (79%) treated with DIAVIS T cells showed response, resulting in significant clinical stabilization or improvement and a reduction in viral load. Six individuals (21%) were classified as nonresponders, deteriorated rapidly, and died, as did 2 other patients during a 12-month follow-up. Older age was the only predictor of a poor treatment response. Survival analysis revealed better 12-month survival rates (hazard ratio, 0.42; 95% CI, 0.24-0.73; P =.02) from diagnosis for patients treated with DIAVIS T cells (18 of 26 [69%]; 12-mo survival rate, 69%) compared with historical controls with BST (57 of 113 [50%]; 12-mo survival rate, including censored data, 45%).

Conclusion and relevance: This case series of DIAVIS T-cell therapy in PML provides first class IV evidence suggesting efficacy to reduce mortality and improve functional outcome. Further prospective studies are required to confirm these results.

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进行性多灶性白质脑病中直接分离的异体病毒特异性 T 细胞
重要性:进行性多灶性白质脑病(PML)是一种危及生命的病毒感染,目前尚无有效的抗病毒治疗方法:目的:确定使用直接分离的异体病毒特异性(DIAVIS)T细胞恢复PML患者受损的免疫系统是否是一种有希望的治疗策略,尤其是在没有其他治疗方案的情况下:2020年3月至2022年2月期间,对接受DIAVIS T细胞治疗的PML患者进行了回顾性病例系列研究。T细胞在24小时内从健康供体中分离出来,针对BK多瘤病毒。PML患者接受单中心治疗。对确诊为PML的患者进行迪亚维斯T细胞治疗资格评估,排除标准包括PML病情稳定和曾接受过纳他珠单抗治疗:新鲜戴维斯T细胞的最大剂量为2×104个CD3+细胞/公斤体重。剩余的T细胞按不同剂量冷冻保存,并在大约2周和6周后进行额外治疗:主要结果和指标:主要结果指标是患者的临床反应和存活率,并与接受最佳支持治疗(BST)的PML病例历史参照组的结果以及最近发表的接受免疫检查点抑制剂治疗的PML患者的实际数据进行比较:研究队列由28名患者组成(中位数[IQR]年龄,60[51-72]岁;20名男性[71.4%])。22 名患者(79%)接受了 DIAVIS T 细胞治疗后出现应答,临床症状明显稳定或改善,病毒载量也有所下降。6名患者(21%)被归类为无应答者,病情迅速恶化并死亡,另外2名患者在12个月的随访期间也死亡了。年龄较大是治疗反应不佳的唯一预测因素。生存分析显示,与使用 BST 的历史对照组(113 人中有 57 人[50%];12 个月生存率,包括删减数据,45%)相比,使用 DIAVIS T 细胞治疗的患者(26 人中有 18 人[69%];12 个月生存率,69%)在确诊后 12 个月的生存率更高(危险比,0.42;95% CI,0.24-0.73;P =.02):迪亚维斯 T 细胞疗法治疗 PML 的病例系列提供了首个 IV 类证据,表明该疗法具有降低死亡率和改善功能预后的疗效。需要进一步的前瞻性研究来证实这些结果。
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来源期刊
JAMA neurology
JAMA neurology CLINICAL NEUROLOGY-
CiteScore
41.90
自引率
1.70%
发文量
250
期刊介绍: JAMA Neurology is an international peer-reviewed journal for physicians caring for people with neurologic disorders and those interested in the structure and function of the normal and diseased nervous system. The Archives of Neurology & Psychiatry began publication in 1919 and, in 1959, became 2 separate journals: Archives of Neurology and Archives of General Psychiatry. In 2013, their names changed to JAMA Neurology and JAMA Psychiatry, respectively. JAMA Neurology is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications.
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