Department of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Cancer Sci. 2012 Nov;103(11):1920-8. doi: 10.1111/j.1349-7006.2012.02410.x. Epub 2012 Sep 28.
The development of peptide vaccines aimed at enhancing immune responses against tumor cells is becoming a promising area of research. Human telomerase reverse transcriptase (hTERT) is an ideal universal target for novel immunotherapies against cancers. The aim of this work was to verify whether the multiple antigen peptides (MAP) based on HLA-A0201-restricted CTL epitopes of hTERT could trigger a better and more sustained CTL response and kill multiple types of hTERT-positive tumor cells in vitro and ex vivo. Dendritic cells (DC) pulsed with MAP based on HLA-A0201-restricted CTL epitopes of hTERT (hTERT-540, hTERT-865 and hTERT-572Y) were used to evaluate immune responses against various tumors and were compared to the immune responses resulting from the use of corresponding linear epitopes and a recombinant adenovirus-hTERT vector. A 4-h standard (51) Cr-release assay and an ELISPOT assay were used for both in vitro and ex vivo analyses. Results demonstrated that targeting hTERT with an adenovector was the most effective way to stimulate a CD8(+) T cell response. When compared with linear hTERT epitopes, MAP could trigger stronger hTERT-specific CTL responses against tumor cells expressing hTERT and HLA-A0201. In contrast, the activated CTL could neither kill the hTERT-negative tumor cells, such as U2OS cells, nor kill HLA-A0201 negative cells, such as HepG2 cells. We also found that these peptide-specific CTL could not kill autologous lymphocytes and DC with low telomerase activity. Our results indicate that MAP from hTERT can be exploited for cancer immunotherapy.
针对肿瘤细胞增强免疫反应的肽疫苗的开发正成为一个有前途的研究领域。人端粒酶逆转录酶(hTERT)是针对癌症的新型免疫疗法的理想通用靶标。本工作旨在验证基于 hTERT 的 HLA-A0201 限制性 CTL 表位的多种抗原肽(MAP)是否可以触发更好、更持久的 CTL 反应,并在体外和体内杀死多种 hTERT 阳性肿瘤细胞。用基于 hTERT 的 HLA-A0201 限制性 CTL 表位(hTERT-540、hTERT-865 和 hTERT-572Y)的 MAP 脉冲的树突状细胞(DC)用于评估针对各种肿瘤的免疫反应,并与使用相应的线性表位和重组腺病毒-hTERT 载体的免疫反应进行比较。使用 4 小时标准(51)Cr 释放测定和 ELISPOT 测定进行体外和体内分析。结果表明,用腺病毒靶向 hTERT 是刺激 CD8(+)T 细胞反应的最有效方法。与线性 hTERT 表位相比,MAP 可以针对表达 hTERT 和 HLA-A0201 的肿瘤细胞触发更强的 hTERT 特异性 CTL 反应。相比之下,激活的 CTL 既不能杀死 hTERT 阴性的肿瘤细胞,如 U2OS 细胞,也不能杀死 HLA-A0201 阴性的细胞,如 HepG2 细胞。我们还发现,这些肽特异性 CTL 不能杀死低端粒酶活性的自体淋巴细胞和 DC。我们的结果表明,hTERT 的 MAP 可用于癌症免疫治疗。