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针对 EBV 相关移植后淋巴组织增生性疾病的 LMP1 特异性细胞毒性 T 细胞治疗。

LMP1-specific cytotoxic T cells for the treatment of EBV-related post-transplantation lymphoproliferative disorders.

机构信息

Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Jixi Road No. 218, Hefei, 230022, Anhui, China.

Shanghai Cancer Institute, Shanghai, 200030, China.

出版信息

Int J Hematol. 2020 Jun;111(6):851-857. doi: 10.1007/s12185-020-02844-7. Epub 2020 Mar 11.

Abstract

Epstein-Barr virus-specific cytotoxic T lymphocytes (EBV-CTLs) represent a promising treatment option for EBV-associated post-transplantation lymphoproliferative disorders (PTLD). However, production of EBV-CTLs is often complicated and expensive. In the present study, we sought to establish an easy-to-use and economical production protocol for EBV-CTLs. EBV-CTLs were generated using latent membrane protein 1 (LMP1) peptides based on a modified generation protocol of cytokine-induced killer (CIK) cells. After 2-week culture, cells were well expanded (median total cell number: 9.82 × 10; median expansion fold: 107.8) and the median EBV LMP1-specific CD8 T cell number was 8.94 × 10 (median frequency: 6.7%). However, the EBV-CTL products, unlike CIK cells, did not exhibit NK-like anti-tumor activity. Furthermore, the clinical efficacy of EBV-CTLs was demonstrated with a successful treatment of PTLD on a compassionate use basis in a patient following haploidentical hematopoietic stem cell transplantation. This study indicates the safety and efficacy of EBV LMP1-specific CTLs generated based on a modified generation protocol of CIK cells. Further investigation in a well-designed clinical study is warranted.

摘要

EBV 特异性细胞毒性 T 淋巴细胞(EBV-CTL)是治疗 EBV 相关移植后淋巴增殖性疾病(PTLD)的有前途的治疗选择。然而,EBV-CTL 的产生通常很复杂且昂贵。在本研究中,我们试图建立一种易于使用且经济的 EBV-CTL 生产方案。基于细胞因子诱导的杀伤(CIK)细胞的改良生成方案,使用潜伏膜蛋白 1(LMP1)肽生成 EBV-CTL。经过 2 周培养,细胞得到了很好的扩增(中位数总细胞数:9.82×10;中位数扩增倍数:107.8),中位数 EBV LMP1 特异性 CD8 T 细胞数为 8.94×10(中位数频率:6.7%)。然而,与 CIK 细胞不同,EBV-CTL 产品不表现出 NK 样抗肿瘤活性。此外,基于 CIK 细胞的改良生成方案生成的 EBV LMP1 特异性 CTL 在 HLA 单倍体造血干细胞移植后患者的同情使用基础上成功治疗 PTLD,证明了其安全性和疗效。这项研究表明,基于 CIK 细胞的改良生成方案生成的 EBV LMP1 特异性 CTL 具有安全性和疗效。需要在精心设计的临床研究中进一步研究。

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