Interleukin-33 upregulation in peripheral leukocytes and CNS of multiple sclerosis patients

被引:86
作者
Christophi, George P. [2 ,4 ]
Gruber, Ross C. [1 ,3 ]
Panos, Michael [1 ]
Christophi, Rebecca L. [2 ]
Jubelt, Burk [1 ,2 ]
Massa, Paul T. [1 ,2 ]
机构
[1] SUNY Syracuse, Upstate Med Univ, Dept Neurol, Syracuse, NY 13210 USA
[2] SUNY Syracuse, Upstate Med Univ, Dept Microbiol & Immunol, Syracuse, NY 13210 USA
[3] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
[4] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
关键词
Autoimmunity; Demyelination; IL-33; Inflammation; Astrocytes; EAE; NF-KAPPA-B; HUMAN MAST-CELLS; INDUCED DEMYELINATING DISEASE; CYTOKINE PRODUCTION; GENE-EXPRESSION; AIRWAY INFLAMMATION; PHOSPHATASE SHP-1; T-CELLS; HUMAN MACROPHAGES; FAMILY-MEMBERS;
D O I
10.1016/j.clim.2011.11.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 beta-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-kappa B 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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:308 / 319
页数:12
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