Cantorna Margherita T, Mahon Brett D
Department of Nutritional Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, USA.
J Rheumatol Suppl. 2005 Sep;76:11-20.
D-hormone [1,25(OH)2 D3] is an important immune system regulator that has been shown to inhibit development of autoimmune diseases including experimental inflammatory bowel disease (IBD), rheumatoid arthritis (RA), multiple sclerosis (MS), and type 1 diabetes. Paradoxically, other immune mediated diseases (experimental asthma) and immunity to infectious organisms were not found to be affected by D-hormone treatment. The effectiveness of D-hormone treatment of autoimmune diseases is due to inhibition of the development and function of Th1 cells and the induction of other Th cells including Th2 cells. We report results of microarray analysis of colons from D-hormone treated mice with experimental IBD. Two hundred thirty-nine genes were inhibited and 298 genes were upregulated in the colon by D-hormone treatment of mice with IBD. Of interest was the D-hormone mediated inhibition of 3 tumor necrosis factor-alpha (TNF-alpha, lipopolysaccharide-induced TNF-alpha factor, and TNF receptor) related genes in the colon. It is likely that the effectiveness of D-hormone treatment of experimental autoimmunity is due in part to the inhibition of the TNF family of genes. D-hormone is a selective regulator of the immune system, and the outcome of D-hormone treatment depends on the nature (infectious disease, asthma, autoimmune disease, etc.) of the immune response.
D激素[1,25(OH)₂D₃]是一种重要的免疫系统调节剂,已被证明可抑制自身免疫性疾病的发展,包括实验性炎症性肠病(IBD)、类风湿性关节炎(RA)、多发性硬化症(MS)和1型糖尿病。矛盾的是,其他免疫介导的疾病(实验性哮喘)以及对感染性生物体的免疫并未发现受D激素治疗的影响。D激素治疗自身免疫性疾病的有效性归因于对Th1细胞发育和功能的抑制以及对包括Th2细胞在内的其他Th细胞的诱导。我们报告了对患有实验性IBD的D激素治疗小鼠的结肠进行微阵列分析的结果。通过对患有IBD的小鼠进行D激素治疗,结肠中有239个基因被抑制,298个基因被上调。有趣的是,D激素介导了结肠中3个与肿瘤坏死因子-α(TNF-α、脂多糖诱导的TNF-α因子和TNF受体)相关基因的抑制。D激素治疗实验性自身免疫的有效性可能部分归因于对TNF基因家族的抑制。D激素是免疫系统的选择性调节剂,D激素治疗的结果取决于免疫反应的性质(传染病、哮喘、自身免疫性疾病等)。