Kim Nayoun, Sohn Hyun-Jung, Oh Joo Hyun, Jeon Young-Woo, Lee Hyun-Joo, Cho Hyun-Il, Chung Byung Ha, Yang Chul-Woo, Kim Tai-Gyu, Cho Seok-Goo
Institute for Translational Research and Molecular Imaging, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, South Korea.
Catholic Institute of Cell Therapy, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Int J Hematol. 2018 May;107(5):596-603. doi: 10.1007/s12185-017-2381-3. Epub 2017 Nov 29.
Conventional therapeutic approaches to post-transplant lymphoproliferative disorder (PTLD) occurring after solid-organ transplantation have shown only limited success in achieving durable response. Key factors driving the pathogenesis of PTLD include Epstein-Barr virus (EBV) reactivation and impaired immune surveillance due to prolonged immune suppression. Thus, EBV-specific cytotoxic T lymphocytes (EBV-CTLs) have emerged as an alternative therapeutic approach for the treatment of EBV-associated PTLD by enhancing EBV-specific immunity. We evaluated the safety and efficacy of EBV latent membrane proteins (LMP)-1- and 2-specific CTLs in two PTLD patients at high risk for relapse. Following diagnosis, patients were initially treated with a combination of chemotherapy and/or radiotherapy. Patients then received a total of eight doses of 2 × 10 EBV-CTLs/m. Following initial therapy, both patients achieved complete remission confirmed by FDG-PET/CT imaging. Post-remission therapy using adoptive transfer of EBV-CTLs was safe without immediate or late toxicities. Infusion of EBV-CTLs led to an overall reduction in plasma EBV levels in the peripheral blood, which was associated with long-term remission of both patients during a follow-up of more than 65 months. Further prospective studies with larger number of patients will be needed to confirm the role of EBV-CTLs as post-remission therapy in high-risk PTLD.
实体器官移植后发生的移植后淋巴细胞增生性疾病(PTLD)的传统治疗方法在实现持久缓解方面仅取得了有限的成功。驱动PTLD发病机制的关键因素包括爱泼斯坦-巴尔病毒(EBV)重新激活以及由于长期免疫抑制导致的免疫监视受损。因此,EBV特异性细胞毒性T淋巴细胞(EBV-CTLs)已成为一种通过增强EBV特异性免疫来治疗EBV相关PTLD的替代治疗方法。我们评估了EBV潜伏膜蛋白(LMP)-1和2特异性CTLs在两名高复发风险PTLD患者中的安全性和疗效。诊断后,患者最初接受化疗和/或放疗联合治疗。然后患者共接受了8剂2×10 EBV-CTLs/m。初始治疗后,两名患者均通过FDG-PET/CT成像确认达到完全缓解。采用EBV-CTLs过继转移的缓解后治疗是安全的,无即刻或晚期毒性。输注EBV-CTLs导致外周血中血浆EBV水平总体降低,这与两名患者在超过65个月的随访期间的长期缓解相关。需要更多患者的进一步前瞻性研究来证实EBV-CTLs作为高危PTLD缓解后治疗的作用。