Kohyama M, Saijyo K, Hayasida M, Yasugi T, Kurimoto M, Ohno T
RIKEN Cell Bank, Institute of Physical and Chemical Research [RIKEN], Ibaraki.
Jpn J Cancer Res. 1998 Oct;89(10):1041-6. doi: 10.1111/j.1349-7006.1998.tb00494.x.
Direct activation of human cytotoxic T lymphocytes (CTL) by interleukin (IL)-18 was observed in a system in which CTL effective against autologous tumor cells were generated. Peripheral blood mononuclear cells (PBMC) from tumor-bearing patients, after removal of natural killer (NK) cells, were cultured in a medium containing IL-1, -2, -4, and -6, with or without IL-18, and stimulated with autologous tumor cells. IL-18 increased the activity of the CTL and the proportion of autologous CD8+ T cells present after 28 days in the induction culture. When purified CD8+ T cells were cultured in the presence of IL-18 and IL-2 for 7 days, the CTL showed enhanced cytotoxic activity against autologous tumor cells. Moreover, a purified CD8+ T cell population, which did not exhibit any apparent cytotoxic activity against autologous tumor cells, displayed cytotoxic activity after 7-day incubation with IL-18. These results suggest that IL-18 may be useful to generate autologous CTL in humans and may thereby contribute to adoptive immunotherapy for tumors.
在一个能产生有效对抗自体肿瘤细胞的细胞毒性T淋巴细胞(CTL)的系统中,观察到白细胞介素(IL)-18可直接激活人CTL。去除自然杀伤(NK)细胞后,取自荷瘤患者的外周血单个核细胞(PBMC)在含有IL-1、-2、-4和-6的培养基中培养,添加或不添加IL-18,并使用自体肿瘤细胞进行刺激。IL-18提高了CTL的活性以及诱导培养28天后出现的自体CD8⁺ T细胞的比例。当纯化的CD8⁺ T细胞在IL-18和IL-2存在的情况下培养7天时,CTL对自体肿瘤细胞的细胞毒性活性增强。此外,一个对自体肿瘤细胞未表现出任何明显细胞毒性活性的纯化CD8⁺ T细胞群体,在与IL-18孵育7天后显示出细胞毒性活性。这些结果表明,IL-18可能有助于在人体内产生自体CTL,从而可能有助于肿瘤的过继性免疫治疗。