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复发/难治性 EB 病毒驱动的移植后淋巴增殖性疾病中的过继性细胞免疫治疗

英文原题:Adoptive Cell Immunotherapy in Relapse/Refractory Epstein-Barr Virus-Driven Post-Transplant Lymphoproliferative Disorders.

查看英文原题

Adoptive Cell Immunotherapy in Relapse/Refractory Epstein-Barr Virus-Driven Post-Transplant Lymphoproliferative Disorders.

PubMed 2025/06/12(内容时间) Antibodies (Basel) Q3 · IF 3.3(JCR 2025)

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中文摘要

移植后淋巴增殖性疾病(PTLD)是实体器官移植(SOT)和异基因造血干细胞移植(allo-HSCT)后一种危及生命的并发症,尤其是在复发/难治性(R/R)疾病患者中,治疗选择有限且预后较差。在新兴策略中,过继性细胞免疫治疗——特别是EB病毒特异性细胞毒性T淋巴细胞(EBV-CTLs)——显著改善了这一具有挑战性患者群体的结局。EBV-CTLs可恢复病毒特异性免疫并诱导持久缓解,且毒性极小,即使在经过大量预处理的患者中也是如此。迄今为止最有前景的细胞产品是tabelecleucel,这是一种即用型异基因EBV特异性T细胞疗法,目前是欧洲药品管理局(EMA)唯一批准用于治疗SOT或allo-HSCT后R/R EBV阳性PTLD的细胞疗法。本综述旨在概述PTLD的治疗,并特别聚焦于过继性细胞免疫治疗。

我们重点介绍EBV-CTLs报告的最稳健的临床结局,尤其是tabelecleucel所取得的结局,并探讨新兴的细胞方法,如CAR-T 细胞疗法,这些方法可能在不久的将来进一步拓宽治疗策略。

展开英文摘要原文

Post-transplant lymphoproliferative disorders (PTLD) represent a life-threatening complication following solid organ transplantation (SOT) and allogeneic hematopoietic stem cell transplantation (allo-HSCT), particularly in patients with relapsed or refractory (R/R) disease, where therapeutic options are limited and prognosis is poor. Among emerging strategies, adoptive cellular immunotherapy-specifically Epstein-Barr virus-specific cytotoxic T lymphocytes (EBV-CTLs)-significantly improved outcomes in this challenging patient population.

EBV-CTLs restore virus-specific immunity and induce sustained remissions with minimal toxicity, even in heavily pretreated individuals. The most promising cellular product to date is tabelecleucel, an off-the-shelf, allogeneic EBV-specific T-cell therapy, which is currently the only cellular therapy approved by the European Medicines Agency (EMA) for the treatment of R/R EBV-positive PTLD following SOT or allo-HSCT. This review aims to provide an overview of PTLD treatment with a specific focus on adoptive cellular immunotherapy.

We highlight the most robust clinical outcomes reported with EBV-CTLs, particularly those achieved with tabelecleucel, and explore emerging cellular approaches such as CAR T-cell therapy, which may further broaden therapeutic strategies in the near future.

论文信息

作者
Canichella M、de Fabritiis P
单位
Hematology, St. Eugenio Hospital, ASL Roma2, 00144 Rome, Italy.Italy
文献类型
综述
期刊
Antibodies (Basel, Switzerland)2025 Jun 12
原文标识
PubMed 40558101 · DOI 10.3390/antib14020047