Jafarirad Sima, Siassi Fereydoon, Harirchian Mohammad-Hossein, Sahraian Mohammad-Ali, Eshraghian Mohammad-Reza, Shokri Fazel, Amani Reza, Bitarafan Sama, Mozafari Sabah, Saboor-Yaraghi Aliakbar
Department of Nutrition and Biochemistry, Tehran University of Medical Sciences, Tehran, Iran.
J Neurosci Rural Pract. 2012 Sep;3(3):294-8. doi: 10.4103/0976-3147.102609.
Multiple sclerosis (MS) is an autoimmune disease whereby myelin sheath of the central nervous system is destroyed. Vitamin A is known to play a role in the immune system. It has been recognized that some metabolites of vitamin A can be used effectively to treat experimental autoimmune encephalomyelitis (EAE).
The effect of vitamin A as retinyl palmitate on T-cell proliferation in MS patients.
This study is a double blind clinical trial of two test groups over a period of 6 months.
Thirty five multiple sclerosis (MS) patients were divided into two groups. One group received 25,000 IU/day vitamin A (as retinyl palmitate) and the other group were administered a placebo. The peripheral blood mononuclear cells (PBMCs) were separated and stimulated with myelin oligodendrocyte glycoprotein (MOG) and phytohemagglutinin (PHA) before and after the trial period. BrdU calorimetric assay was performed to measure cell proliferation.
Analysis of covariance (ANCOVA) and paired t-test were used to analyze the data.
Observations showed statistical significant differences in the reduction of cell proliferation in the presence of MOG and fetal calf serum (FCS) in the culture medium, between patients receiving vitamin A and the placebo (P = 0.046). Although, this difference was not significant between the two vitamin A and placebo groups in MOG treatment with human serum, a decrease was observed in the group of patients taking vitamin A supplements (P = 0.019). Phytohemagglutinin did not cause any change in cell proliferation between the two groups.
The results suggest supplementation with retinyl palmitate in patients with MS reduce MOG stimulatory effects on T-cells.
多发性硬化症(MS)是一种自身免疫性疾病,中枢神经系统的髓鞘会被破坏。已知维生素A在免疫系统中发挥作用。人们已经认识到维生素A的一些代谢产物可有效用于治疗实验性自身免疫性脑脊髓炎(EAE)。
维生素A棕榈酸酯对MS患者T细胞增殖的影响。
本研究是一项针对两个试验组为期6个月的双盲临床试验。
35例多发性硬化症(MS)患者被分为两组。一组每天接受25,000国际单位的维生素A(以棕榈酸视黄酯形式),另一组给予安慰剂。在试验期前后分离外周血单个核细胞(PBMC),并用髓鞘少突胶质细胞糖蛋白(MOG)和植物血凝素(PHA)进行刺激。采用BrdU比色法测定细胞增殖。
采用协方差分析(ANCOVA)和配对t检验分析数据。
观察结果显示,在培养基中存在MOG和胎牛血清(FCS)的情况下,接受维生素A治疗的患者与接受安慰剂治疗的患者相比,细胞增殖减少具有统计学显著差异(P = 0.046)。尽管在用人类血清进行MOG治疗时,维生素A组和安慰剂组之间的这种差异不显著,但服用维生素A补充剂的患者组中观察到了下降(P = 0.019)。植物血凝素在两组之间未引起细胞增殖的任何变化。
结果表明,MS患者补充棕榈酸视黄酯可降低MOG对T细胞的刺激作用。