Saeki R, Ogino H, Kaneko S, Unoura M, Kobayashi K
First Department of Internal Medicine, Kanazawa University, Ishikawa, Japan.
J Gastroenterol. 1995 Dec;30(6):739-44. doi: 10.1007/BF02349640.
Ursodeoxycholic acid (UDCA) administration can obtain marked improvement of primary biliary cirrhosis (PBC). Recently, UDCA has been demonstrated to have a direct effect on immunological reactions in patients with PBC in that the aberrant expression of major histocompatibility complex (MHC) class I molecules was markedly reduced after UDCA treatment. To understand the immunological effect of UDCA, we analyzed interferon (IFN)-gamma production in peripheral blood mononuclear cells (PBMCs) from 29 patients with PBC treated with UDCA (group 1), 19 patients with PBC who were not treated with UDCA (group 2), 11 healthy subjects (group 3), and 12 patients with chronic viral hepatitis (group 4). IFN-gamma production was investigated because the excess production of this cytokine is associated with the aberrant expression of MHC molecules. Whereas IFN-gamma production in the patients in group 2 was significantly increased, the level of production in group 1 was similar to that in the control groups (groups 3 and 4). There was significant improvement in IFN-gamma production in 6 patients with PBC after UDCA treatment. The effect of UDCA and chenodeoxycholic acid (CDCA) on IFN-gamma production in PBMCs from 12 normal subjects was also analyzed. IFN-gamma was produced dose-dependently according to concentrations of CDCA ranging from 0.1 to 10 microM, but the increase in production was markedly suppressed by the addition of UDCA. We conclude that low doses of CDCA enhance IFN-gamma production and may therefore lead to the aberrant hepatic expression of MHC molecules, and that the increase in IFN-gamma production is suppressed by UDCA.
熊去氧胆酸(UDCA)治疗可使原发性胆汁性肝硬化(PBC)得到显著改善。最近,已证明UDCA对PBC患者的免疫反应有直接影响,因为在UDCA治疗后,主要组织相容性复合体(MHC)I类分子的异常表达明显降低。为了解UDCA的免疫作用,我们分析了29例接受UDCA治疗的PBC患者(第1组)、19例未接受UDCA治疗的PBC患者(第2组)、11名健康受试者(第3组)和12例慢性病毒性肝炎患者(第4组)外周血单个核细胞(PBMC)中干扰素(IFN)-γ的产生情况。研究IFN-γ的产生是因为这种细胞因子的过量产生与MHC分子的异常表达有关。第2组患者的IFN-γ产生显著增加,而第1组的产生水平与对照组(第3组和第4组)相似。6例PBC患者经UDCA治疗后IFN-γ产生有显著改善。还分析了UDCA和鹅去氧胆酸(CDCA)对12名正常受试者PBMC中IFN-γ产生的影响。根据0.1至10 microM的CDCA浓度,IFN-γ呈剂量依赖性产生,但加入UDCA后产生的增加受到明显抑制。我们得出结论,低剂量的CDCA增强IFN-γ的产生,因此可能导致肝脏中MHC分子的异常表达,而UDCA可抑制IFN-γ产生的增加。