Kang B Y, Chung S W, Im S Y, Choe Y K, Kim T S
College of Pharmacy, Chonnam National University, Kwangju, Republic of Korea.
Immunology. 1999 Sep;98(1):98-103. doi: 10.1046/j.1365-2567.1999.00849.x.
Interleukin-12 (IL-12) plays a pivotal role in the development of T-helper 1 (Th1) immune response, which may be involved in the pathogenesis of chronic inflammatory autoimmune disorders. In this study we investigated the effects of sulfasalazine, a drug for treating inflammatory bowel disease and rheumatoid arthritis, on the production of IL-12 from mouse macrophages stimulated with lipopolysaccharide (LPS). Sulfasalazine potently inhibited the production of IL-12 in a dose-dependent manner, in part through the down-regulation of nuclear factor kappaB (NFkappaB) activation in IL-12 p40 gene. Activation of macrophages by LPS resulted in markedly enhanced binding activities to the kappaB site, which significantly decreased upon addition of sulfasalazine as demonstrated by an electrophoretic gel shift assay. Importantly, macrophages pretreated with sulfasalazine either in vitro or in vivo reduced their ability to induce interferon-gamma (IFN-gamma) and increased the ability to induce IL-4 in antigen-primed CD4+ T cells. From these results, sulfasalazine may induce the Th2 cytokine profile in CD4+ T cells by suppressing IL-12 production in macrophages, and sulfasalazine-induced inhibition of IL-12 production in macrophages may explain some of the known biological effects of sulfasalazine.
白细胞介素-12(IL-12)在辅助性T细胞1(Th1)免疫反应的发展中起关键作用,这可能参与慢性炎症性自身免疫性疾病的发病机制。在本研究中,我们调查了用于治疗炎症性肠病和类风湿性关节炎的药物柳氮磺胺吡啶对脂多糖(LPS)刺激的小鼠巨噬细胞产生IL-12的影响。柳氮磺胺吡啶以剂量依赖性方式有效抑制IL-12的产生,部分是通过下调IL-12 p40基因中的核因子κB(NFκB)激活。LPS激活巨噬细胞导致与κB位点的结合活性显著增强,如电泳凝胶迁移试验所示,加入柳氮磺胺吡啶后这种结合活性显著降低。重要的是,在体外或体内用柳氮磺胺吡啶预处理的巨噬细胞降低了其在抗原致敏的CD4 + T细胞中诱导干扰素-γ(IFN-γ)的能力,并增加了诱导IL-4的能力。从这些结果来看,柳氮磺胺吡啶可能通过抑制巨噬细胞中IL-12的产生来诱导CD4 + T细胞中的Th2细胞因子谱,并且柳氮磺胺吡啶诱导的巨噬细胞中IL-12产生的抑制可能解释了柳氮磺胺吡啶的一些已知生物学效应。