Ford Lara, Rowe Dominic
Northern Clinical School, Faculty of Medicine, University of Sydney, Australia.
Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Jun;5(2):118-20. doi: 10.1080/14660820410019125.
The cause of sporadic amyotrophic lateral sclerosis (SALS) is unknown. We investigated the immune-mediated inflammatory hypothesis of SALS by assaying interleukin-12 (IL-12), interleukin-6 (IL-6) and interferon-gamma (IFN-gamma) in the cerebrospinal fluid (CSF) of patients with SALS. These cytokines were measured in the CSF from patients with SALS (n=11), patients with immune-mediated inflammatory central nervous system or nerve root disorders (n=12), and patients with other neurological diseases (n=15) by high sensitivity sandwich enzyme linked immunosorbent assay (ELISA). All samples were below the assay detection limits of 0.5 pg/ml for IL-12 and 8 pg/ml for IFN-gamma. There was no difference between the groups in the mean concentration of IL-6. There is no evidence in cerebrospinal fluid for induction of a T(H)1 immune response in SALS.
散发性肌萎缩侧索硬化症(SALS)的病因尚不清楚。我们通过检测SALS患者脑脊液(CSF)中的白细胞介素-12(IL-12)、白细胞介素-6(IL-6)和干扰素-γ(IFN-γ),研究了SALS的免疫介导炎症假说。采用高灵敏度夹心酶联免疫吸附测定(ELISA)法,对11例SALS患者、12例免疫介导炎症性中枢神经系统或神经根疾病患者以及15例其他神经系统疾病患者的脑脊液中的这些细胞因子进行了检测。所有样本中IL-12的浓度均低于0.5 pg/ml的检测限,IFN-γ的浓度均低于8 pg/ml的检测限。各组间IL-6的平均浓度无差异。脑脊液中没有证据表明SALS患者存在T(H)1免疫反应的诱导。