Kivisäkk P, Tian W, Matusevicius D, Link H, Söderström M
Division of Neurology, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden.
Neurology. 1998 Jan;50(1):217-23. doi: 10.1212/wnl.50.1.217.
Acute unilateral monosymptomatic optic neuritis (ON) is a common first manifestation of MS if associated with multiple MS-like lesions on brain MRI and oligoclonal IgG bands (OB) in the CSF, whereas ON patients lacking these laboratory abnormalities are considered to have a good prognosis regarding future MS development. Several cytokines involved in immune regulation are upregulated in blood and even more noticeable in CSF in MS. To study a possible relation between cytokine profiles and presence versus absence of MS-like brain MRI lesions and CSF OB, we used in situ hybridization to examine mRNA expression of the proinflammatory interleukin-12 (IL-12), interferon-gamma, and tumor necrosis factor-alpha and the immune response downregulating IL-10, transforming growth factor-beta, and IL-4 in blood and CSF mononuclear cells (MNC) from 59 patients with untreated ON. There were no differences in numbers of MNC in blood or CSF expressing any of the cytokines under study, upon subgrouping the ON patients regarding presence (n = 31) versus absence (n = 28) of MRI lesions, presence (n = 45) versus absence (n = 14) of OB, or duration after onset of ON (<1 month, n = 30, versus >1 month, n = 29). Similarly, no differences were observed for numbers of myelin basic protein-reactive blood MNC expressing any of these cytokines after subgrouping according to these variables. Our findings suggest that the cytokine profile, as examined in this study, is less useful to determine the risk of future development of clinically definite MS in ON patients or as indicator for therapeutic interventions in ON. An upregulation of both pro- and anti-inflammatory cytokines in ON patients seems to be more related to the CNS disease per se, whether limited to the optic nerve or not, than to the inflammatory process characteristic for MS.
急性单侧单症状性视神经炎(ON)如果与脑部MRI上的多个类似多发性硬化症(MS)的病灶以及脑脊液中的寡克隆IgG带(OB)相关,则是MS常见的首发表现,而缺乏这些实验室异常的ON患者被认为未来发生MS的预后良好。在MS患者中,几种参与免疫调节的细胞因子在血液中上调,在脑脊液中更为明显。为了研究细胞因子谱与是否存在类似MS的脑部MRI病灶及脑脊液OB之间的可能关系,我们采用原位杂交技术检测了59例未经治疗的ON患者血液和脑脊液单核细胞(MNC)中促炎细胞因子白细胞介素-12(IL-12)、干扰素-γ和肿瘤坏死因子-α以及下调免疫反应的细胞因子IL-10、转化生长因子-β和IL-4的mRNA表达。根据MRI病灶的有无(存在组n = 31,不存在组n = 28)、OB的有无(存在组n = 45,不存在组n = 14)或ON发病后的病程(<1个月组n = 30,>1个月组n = 29)对ON患者进行亚组分析后,表达所研究的任何一种细胞因子的血液或脑脊液中的MNC数量均无差异。同样地,根据这些变量进行亚组分析后,表达这些细胞因子的髓鞘碱性蛋白反应性血液MNC数量也未观察到差异。我们的研究结果表明,本研究中检测的细胞因子谱对于确定ON患者未来发生临床确诊MS的风险或作为ON治疗干预的指标作用较小。ON患者中促炎和抗炎细胞因子的上调似乎更多地与中枢神经系统疾病本身相关,无论是否局限于视神经,而不是与MS特有的炎症过程相关。