Luo Yunping, Zhou He, Mizutani Masato, Mizutani Noriko, Liu Cheng, Xiang Rong, Reisfeld Ralph A
Department of Immunology, Scripps Research Institute, La Jolla, CA 92037, USA.
Cancer Res. 2005 Apr 15;65(8):3419-27. doi: 10.1158/0008-5472.CAN-04-3120.
A novel vaccination strategy induced specific CD8(+) T cell-mediated immunity that eradicated spontaneous and experimental pulmonary cancer metastases in syngeneic mice and was also effective in a therapeutic setting of established breast cancer metastases. This was achieved by targeting transcription factor Fos-related antigen 1(Fra-1), overexpressed by many tumor cells, with an ubiquitinated DNA vaccine against Fra-1, coexpressing secretory IL-18. Insight into the immunologic mechanisms involved was provided by adoptive transfer of T lymphocytes from successfully immunized BALB/c mice to syngeneic severe combined immunodeficient (SCID) mice. Specifically, long-lived T memory cells were maintained dormant in nonlymphoid tissues by IL-18 in the absence of tumor antigen. Importantly, a second tumor cell challenge of these SCID mice restored both, robust tumor-specific cytotoxicity and long-lived T-cell memory, capable of eradicating established pulmonary cancer metastases, suggesting that this vaccine could be effective against tumor recurrence.
一种新型疫苗接种策略可诱导特异性CD8(+) T细胞介导的免疫反应,该反应能根除同基因小鼠体内自发形成的和实验性的肺癌转移灶,并且在已形成乳腺癌转移灶的治疗环境中也有效。这是通过用一种针对转录因子Fos相关抗原1(Fra-1)的泛素化DNA疫苗来实现的,Fra-1在许多肿瘤细胞中过表达,该疫苗还共表达分泌性白细胞介素-18(IL-18)。通过将成功免疫的BALB/c小鼠的T淋巴细胞过继转移到同基因严重联合免疫缺陷(SCID)小鼠体内,深入了解了其中涉及的免疫机制。具体而言,在没有肿瘤抗原的情况下,长寿T记忆细胞通过IL-18在非淋巴组织中保持休眠状态。重要的是,对这些SCID小鼠进行第二次肿瘤细胞攻击可恢复强大的肿瘤特异性细胞毒性和长寿T细胞记忆,能够根除已形成的肺癌转移灶,这表明该疫苗可能对肿瘤复发有效。