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