Department of Gastroenterology, The Shenyang General Hospital of PLA, No. 83 Wenhua Road, Shenyang City, Liaoning, China.
Vaccine. 2013 Sep 23;31(41):4585-90. doi: 10.1016/j.vaccine.2013.07.055. Epub 2013 Aug 6.
Pancreatic cancer (PC) is one of the most devastating human malignancies without effective therapies. Tumor vaccine based on RNA-transfected dendritic cells (DCs) has emerged as an alternative therapeutic approach for a variety of human cancers including advanced PC. In the present study we compared the cytotoxic T lymphocyte (CTL) responses against PC cells in vitro, which were induced by DCs co-transfected with two mRNAs of tumor associated-antigens (TAA) MUC4 and survivin, versus DCs transfected with a single mRNA encoding either MUC4 or survivin. DCs co-transfected with two TAA mRNAs were found to induce stronger CTL responses against PC target cells in vitro, compared with the DCs transfected with a single mRNA. Moreover, the antigen-specific CTL responses were MHC class I-restricted. These results provide an experimental foundation for further clinical investigations of DC vaccines encoding multiple TAA epitopes for metastatic PC.
胰腺癌(PC)是一种最具破坏性的人类恶性肿瘤,目前尚无有效的治疗方法。基于 RNA 转染树突状细胞(DC)的肿瘤疫苗已成为多种人类癌症(包括晚期 PC)的一种替代治疗方法。在本研究中,我们比较了 DC 共转染两种肿瘤相关抗原(TAA)MUC4 和 survivin 的 mRNA 与 DC 转染单个编码 MUC4 或 survivin 的 mRNA 后体外诱导针对 PC 细胞的细胞毒性 T 淋巴细胞(CTL)反应。结果发现,与转染单个 mRNA 的 DC 相比,共转染两种 TAA mRNA 的 DC 可诱导更强的针对 PC 靶细胞的 CTL 反应。此外,抗原特异性 CTL 反应受到 MHC Ⅰ类限制。这些结果为进一步研究针对转移性 PC 的编码多个 TAA 表位的 DC 疫苗的临床应用提供了实验基础。