Department of Biotechnology and Therapeutics, Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
Biochem Biophys Res Commun. 2010 Mar 26;394(1):54-8. doi: 10.1016/j.bbrc.2010.02.085. Epub 2010 Feb 18.
Cytotoxic T lymphocytes (CTL) are critical effector cells in tumor immunity. Adoptive transfer therapy with in vitro-expanded tumor-specific CTL is a promising approach for preventing cancer metastasis and recurrence. Transferred CTL are not effective in clinical trials, however, due to inadequate tumor-infiltration. Therefore, the development of functionally modified CTL, such as tumor-targeting CTL, is widely desired. Here, we designed the tumor-targeting CTL expressing a single-chain antibody fragment (scFv-CTL) specific for vascular endothelial growth factor receptor 2 (VEGFR2/flk1) by transducing the CTL with a retroviral vector. The scFv-CTL bound to VEGFR2/flk1-expressing cells and retained their cytotoxic activity against tumor cells. In addition, adoptive transfer of scFv-CTL into tumor-bearing mice effectively suppressed tumor growth due to the augmented accumulation of the transferred CTL in the tumor tissue. These findings indicate that the creation of CTL capable of targeting tumor vascular endothelial cells by scFv-expression technique is considerably promising for improvement of efficacy in adoptive immunotherapy.
细胞毒性 T 淋巴细胞(CTL)是肿瘤免疫中的关键效应细胞。体外扩增的肿瘤特异性 CTL 的过继转移治疗是预防癌症转移和复发的一种很有前途的方法。然而,由于转移瘤组织中 CTL 浸润不足,转移 CTL 在临床试验中效果不佳。因此,广泛需要开发功能修饰的 CTL,如肿瘤靶向 CTL。在此,我们通过逆转录病毒载体转导 CTL,设计了表达针对血管内皮生长因子受体 2(VEGFR2/flk1)的单链抗体片段(scFv-CTL)的肿瘤靶向 CTL。scFv-CTL 与表达 VEGFR2/flk1 的细胞结合,并保留其对肿瘤细胞的细胞毒性活性。此外,由于转导的 CTL 在肿瘤组织中的积累增加,将 scFv-CTL 过继转移到荷瘤小鼠中可有效抑制肿瘤生长。这些发现表明,通过 scFv 表达技术创建能够靶向肿瘤血管内皮细胞的 CTL,对于提高过继免疫治疗的疗效具有很大的潜力。