Early administration of IL-12 suppresses EAE through induction of interferon-γ

被引:36
作者
Gran, B
Chu, NS
Zhang, GX
Yu, S
Li, YH
Chen, XH
Kamoun, M
Rostami, A
机构
[1] Thomas Jefferson Univ, Dept Neurol, Philadelphia, PA 19107 USA
[2] Univ Penn, Sch Med, Dept Neurosurg, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
EAE; cytokines; autoimmunity; rodent; transgenic/knockout;
D O I
10.1016/j.jneuroim.2004.07.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent findings have shown that IL-12, a key inducer of Th1 cell development, is not required in the pathogenesis of experimental autoimmune encephalomyelitis (EAE) as severe CNS inflammatory demyelination can develop in the absence of IL-12 or IL-12 responsiveness. These data raised the possibility of an immunomodulatory action of IL-12 in this disease model. We show here that IL-12 suppresses MOG35-55-induced EAE in the C57BL/6 mouse when administered during the early induction phase of the disease. The inhibitory effect is interferon-gamma-(IFN-gamma)-dependent, as clearly shown by lack of suppression in IFN-gamma-deficient mice, and is also accompanied by inhibition of mRNA expression of the proinflammatory cytokine IL-17. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 131
页数:9
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