Hussien Yassir, Sanna Alessandra, Söderström Mats, Link Hans, Huang Yu-Min
Neurotec Department, Division of Neuroimmunology, Karolinska Institute, Alfred Nobels Alle 10, Stockholm, Sweden.
Mult Scler. 2004 Feb;10(1):16-25. doi: 10.1191/1352458504ms979oa.
Current therapy of multiple sclerosis (MS) with interferon-beta (IFN-beta) or glatiramer acetate (GA) has modest effects on the course of MS. Both compounds affect several immune variables, like expression of cell surface molecules and cytokine levels. Here we compared untreated MS, therapy with IFN-beta alone and combined with GA, and healthy controls (HC), regarding expression on HLA-DR+ blood mononuclear cells (MNC) of CD1a that is a cell surface molecule with capacity to present glycolipids to T cells, and of CD80 and CD86 which are costimulatory molecules that activate Th1 and Th2 responses. Cytokine production by MNC was also measured. Flow cytometry and ELISA were used. Cross-sectional comparisons revealed that untreated MS patients had higher CD1a+ HLA-DR+ MNC and lower IL-10 production compared to patients treated with IFN-beta or IFN-beta+GA or HC. Untreated MS patients also had higher spontaneous IFN-gamma and IL-12p70 production compared to MS patients treated with IFN-beta+GA or HC, but not when compared to MS patients on monotherapy with IFN-beta. Low CD1a+ HLA-DR+ MNC and low spontaneous production of IL-12p70 and IFN-gamma were more pronounced in patients treated with IFN-beta+GA than with IFN-beta alone. In order to clarify whether these changes reflect disease activity or treatment effects, we performed a follow up study. Nineteen MS patients with disease progression, despite monotherapy with IFN-beta for more than one year; were re-examined after one to three and four to six months of treatment with IFN-beta+GA. This combination therapy was associated with normalization of CD1a+ HLA-DR+ MNC, IL-12p70 and IFN-gamma. It remains to be shown whether these immunological changes imply a clinical benefit. Follow up studies of immune variables versus clinical effects during combined therapy of MS with IFN-beta+GA are ongoing.
目前使用β-干扰素(IFN-β)或醋酸格拉替雷(GA)治疗多发性硬化症(MS)对MS病程的影响不大。这两种化合物都会影响多个免疫变量,如细胞表面分子的表达和细胞因子水平。在此,我们比较了未经治疗的MS患者、单独使用IFN-β治疗以及联合GA治疗的患者,和健康对照(HC),观察具有向T细胞呈递糖脂能力的细胞表面分子CD1a、以及激活Th1和Th2反应的共刺激分子CD80和CD86在HLA-DR⁺血液单核细胞(MNC)上的表达情况。还检测了MNC产生的细胞因子。使用了流式细胞术和酶联免疫吸附测定法。横断面比较显示,与接受IFN-β或IFN-β + GA治疗的患者或HC相比,未经治疗的MS患者具有更高的CD1a⁺ HLA-DR⁺ MNC和更低的IL-10产生量。与接受IFN-β + GA治疗的MS患者或HC相比,未经治疗的MS患者还具有更高的自发性IFN-γ和IL-12p70产生量,但与接受IFN-β单一疗法的MS患者相比则不然。与单独使用IFN-β治疗的患者相比,接受IFN-β + GA治疗的患者中低CD1a⁺ HLA-DR⁺ MNC以及低自发性IL-12p70和IFN-γ产生更为明显。为了阐明这些变化是反映疾病活动还是治疗效果,我们进行了一项随访研究。19例尽管接受IFN-β单一疗法治疗超过一年但疾病仍进展的MS患者,在接受IFN-β + GA治疗1至3个月以及4至6个月后重新接受检查。这种联合疗法与CD1a⁺ HLA-DR⁺ MNC、IL-12p70和IFN-γ的正常化相关。这些免疫变化是否意味着临床益处仍有待证明。MS患者接受IFN-β + GA联合治疗期间免疫变量与临床效果的随访研究正在进行中。