Department of Microbiology & Immunology, Upstate Medical University State University of New York, 750 East Adams Street, Syracuse, NY 13210, USA.
Clin Immunol. 2012 Mar;142(3):308-19. doi: 10.1016/j.clim.2011.11.007. Epub 2011 Dec 2.
Multiple sclerosis (MS) is an immune-mediated demyelinating disease of the central nervous system (CNS). Here we document for the first time that the cytokine IL-33 is upregulated in both the periphery and the CNS of MS patients. Plasma IL-33 was elevated in MS patients compared to normal subjects and a three-month treatment of MS patients with interferon β-1a resulted in a significant decrease of IL-33 levels. Similarly, stimulated cultured lymphocytes and macrophages from MS patients had elevated IL-33 levels compared to normal subjects. In parallel, the transcription factor NF-κB that mediates IL-33 transcription was also elevated in leukocytes of MS patients. IL-33 was elevated in normal-appearing white matter and plaque areas from MS brains and astrocytes were identified as an important source of IL-33 expression in the CNS. In summary, IL-33 levels are elevated in the periphery and CNS of MS patients, implicating IL-33 in the pathogenesis of MS.
多发性硬化症(MS)是一种中枢神经系统(CNS)的免疫介导的脱髓鞘疾病。在这里,我们首次记录到细胞因子 IL-33 在 MS 患者的外周血和中枢神经系统中均上调。与正常对照相比,MS 患者的血浆 IL-33 水平升高,而用干扰素β-1a 治疗 MS 患者三个月可导致 IL-33 水平显著下降。类似地,与正常对照相比,来自 MS 患者的刺激培养的淋巴细胞和巨噬细胞具有更高的 IL-33 水平。平行地,介导 IL-33 转录的转录因子 NF-κB 在 MS 患者的白细胞中也升高。IL-33 在 MS 大脑的正常外观白质和斑块区域中升高,星形胶质细胞被鉴定为 CNS 中 IL-33 表达的重要来源。总之,IL-33 水平在 MS 患者的外周血和中枢神经系统中升高,提示 IL-33 参与 MS 的发病机制。