Hao Jing-Sheng, Shan Bao-En
Research Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China.
Cancer Immunol Immunother. 2006 Nov;55(11):1426-31. doi: 10.1007/s00262-006-0171-5. Epub 2006 May 5.
Immunotherapy, including the use of cytokines and/or modified tumour cells immune stimulatory cytokines, can enhance the host anti-tumour immune responses. Interleukin-23 (IL-23) is a relative novel cytokine, which consists of a heterodimer of the IL-12p40 subunit and a novel p19 subunit. IL-23 has biological activities similar to but distinct from IL-12. IL-23 can enhance the proliferation of memory T cells and the production of IFN-gamma, IL-12 and TNF-alpha from activated T cells. IL-23 activates macrophages to produce TNF-alpha and nitric oxide. IL-23 can also act directly on dendritic cells and possesses potent anti-tumour and anti-metastatic activity in murine models of cancer. IL-23 can also induce a lower level of IFN-gamma production compared with that induced by IL-12. This may make IL-23 an alternative and safer therapeutic agent for cancer, as IL-12 administration can lead to severe toxic side effects because of the extremely high levels of IFN-gamma it induces.
免疫疗法,包括使用细胞因子和/或经修饰的肿瘤细胞免疫刺激细胞因子,可增强宿主抗肿瘤免疫反应。白细胞介素-23(IL-23)是一种相对较新的细胞因子,它由IL-12p40亚基和一个新的p19亚基组成的异二聚体。IL-23具有与IL-12相似但又不同的生物学活性。IL-23可增强记忆T细胞的增殖以及活化T细胞产生干扰素-γ、IL-12和肿瘤坏死因子-α。IL-23激活巨噬细胞产生肿瘤坏死因子-α和一氧化氮。IL-23还可直接作用于树突状细胞,并在小鼠癌症模型中具有强大的抗肿瘤和抗转移活性。与IL-12诱导产生的干扰素-γ水平相比,IL-23诱导产生的干扰素-γ水平也较低。这可能使IL-23成为一种替代的、更安全的癌症治疗药物,因为给予IL-12会由于其诱导产生的极高水平的干扰素-γ而导致严重的毒副作用。