Interleukin-15 and Interleukin-12 Are Elevated in Serum and Cerebrospinal Fluid of Patients with Amyotrophic Lateral Sclerosis

肌萎缩侧索硬化 脑脊液 医学 促炎细胞因子 免疫学 多发性硬化 白细胞介素 免疫系统 发病机制 疾病 细胞因子 内科学 炎症
作者
Michael Rentzos,Antonis Rombos,Chryssoula Nikolaou,Margarita Zoga,Vasiliki Zouvelou,A. Dimitrakopoulos,Theodoros Alexakis,Anthousa Tsoutsou,Anastasia Samakovli,Maria Michalopoulou,Ioannis Evdokimidis
出处
期刊:European Neurology [Karger Publishers]
卷期号:63 (5): 285-290 被引量:45
标识
DOI:10.1159/000287582
摘要

There is evidence that immunological factors may be involved in pathogenic mechanisms of amyotrophic lateral sclerosis (ALS). Interleukin (IL)-15 and IL-12 are proinflammatory cytokines produced by activated blood and glial cells. They promote T cell differentiation and proliferation.We measured by ELISA serum and cerebrospinal fluid (CSF) levels of IL-15 and IL-12 in 21 patients with ALS and 19 patients with other noninflammatory neurological disorders (NIND) studied as a control group. IL-15 and IL-12 serum and CSF levels were also correlated with duration of the disease, the disability level determined using the revised ALS Functional Rating Scale and the clinical subtype of the disease onset in patients with ALS.IL-15 and IL-12 serum levels were higher in patients with ALS as compared with patients with NIND (p = 0.014 and p = 0.011, respectively). IL-15 and IL-12 CSF levels were also increased in patients with ALS (p = 0.011 and p = 0.005, respectively). IL-15 and IL-12 levels were not correlated with disease duration, disability scale or clinical subtype of the disease onset in ALS patients.Our findings suggest that these molecules may be involved in the pathogenic mechanisms acting as potential markers of immune activation in ALS.
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