首页> 外文期刊>Molecular therapy: the journal of the American Society of Gene Therapy >Long-term Outcome of Extranodal NK/T Cell Lymphoma Patients Treated With Postremission Therapy Using EBV LMP1 and LMP2a-specific CTLs
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Long-term Outcome of Extranodal NK/T Cell Lymphoma Patients Treated With Postremission Therapy Using EBV LMP1 and LMP2a-specific CTLs

机译:使用EBV LMP1和LMP2a特异性CTL进行缓解后治疗的结外NK / T细胞淋巴瘤患者的长期结果

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Extranodal NK/T-cell lymphoma (ENKTCL) is associated with latent Epstein-Barr virus (EBV) infection and frequent relapse even after complete response (CR) to intensive chemotherapy and radiotherapy. The expression of EBV proteins in the tumor provides targets for adoptive immunotherapy with antigen-specific cytotoxic T cells (CTL). To evaluate the efficacy and safety of EBV latent membrane protein (LMP)-1 and -LMP-2a-specific CTLs (LMP1/2a CTLs) stimulated with LMP1/2a -RNA-transferred dendritic cells, we treated 10 ENKTCL patients who showed complete response to induction therapy. Patients who completed and responded to chemotherapy, radiotherapy, and/or high-dose therapy followed by stem cell transplantation (HDT/SCT) were eligible to receive eight doses of 2 x 10(7) LMP1/2a CTLs/m(2). Following infusion, there were no immediate or delayed toxicities. The 4-year overall survival (OS) and progression-free survival (PFS) were 100%, and 90% (95% CI: 71.4 to 100%) respectively with a median follow-up of 55.5 months. Circulating IFN-gamma secreting LMP1 and LMP2a-specific T cells within the peripheral blood corresponded with decline in plasma EBV DNA levels in patients. Adoptive transfer of LMP1/2a CTLs in ENKTCL patients is a safe and effective postremission therapeutic approach. Further randomized studies will be needed to define the role of EBV-CTLs in preventing relapse of ENKTCL.
机译:结外NK / T细胞淋巴瘤(ENKTCL)与潜伏的爱泼斯坦-巴尔病毒(EBV)感染相关,即使在对强化化学疗法和放疗的完全反应(CR)之后也经常复发。 EBV蛋白在肿瘤中的表达为抗原特异性细胞毒性T细胞(CTL)的过继免疫疗法提供了靶点。为了评估由LMP1 / 2a -RNA转移的树突状细胞刺激的EBV潜伏膜蛋白(LMP)-1和-LMP-2a特异性CTL(LMP1 / 2a CTL)的疗效和安全性,我们治疗了10例表现完整的ENKTCL患者对诱导疗法的反应。完成化学疗法,放射疗法和/或大剂量疗法并随后进行干细胞移植(HDT / SCT)并对其做出反应的患者,有资格接受八剂2 x 10(7)LMP1 / 2a CTLs / m(2)。输注后,没有立即或延迟的毒性。 4年总生存(OS)和无进展生存(PFS)分别为100%和90%(95%CI:71.4至100%),中位随访时间为55.5个月。外周血中循环分泌IFN-γ的LMP1和LMP2a特异性T细胞与患者血浆EBV DNA水平下降相对应。在ENKTCL患者中过转移LMP1 / 2a CTL是一种安全有效的缓解后治疗方法。需要进一步的随机研究来确定EBV-CTL在预防ENKTCL复发中的作用。

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