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复发/难治性爱泼斯坦-巴尔病毒驱动的移植后淋巴细胞增生性疾病的过继性细胞免疫治疗

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

作者信息

Canichella Martina, de Fabritiis Paolo

机构信息

Hematology, St. Eugenio Hospital, ASL Roma2, 00144 Rome, Italy.

Department of Biomedicina e Prevenzione, Tor Vergata University, 00133 Rome, Italy.

出版信息

Antibodies (Basel). 2025 Jun 12;14(2):47. doi: 10.3390/antib14020047.

Abstract

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.

摘要

移植后淋巴细胞增生性疾病(PTLD)是实体器官移植(SOT)和异基因造血干细胞移植(allo-HSCT)后的一种危及生命的并发症,尤其是在复发或难治性(R/R)疾病患者中,这类患者的治疗选择有限且预后较差。在新兴策略中,过继性细胞免疫疗法,特别是爱泼斯坦-巴尔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的患者群体的治疗结果。EBV-CTLs可恢复病毒特异性免疫,并以最小的毒性诱导持续缓解,即使是在经过大量预处理的个体中也是如此。迄今为止最有前景的细胞产品是tabelecleucel,这是一种现成的、异基因的EBV特异性T细胞疗法,目前是欧洲药品管理局(EMA)批准的唯一用于治疗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,特别关注过继性细胞免疫疗法。我们重点介绍了EBV-CTLs报告的最有力的临床结果,尤其是tabelecleucel所取得的结果,并探讨了如嵌合抗原受体T细胞疗法等新兴细胞方法,这些方法可能在不久的将来进一步拓宽治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a38b/12189535/114f4047936d/antibodies-14-00047-g001.jpg

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