Mice lacking myeloperoxidase are more susceptible to experimental autoimmune encephalomyelitis

被引:68
作者
Brennan, ML
Gaur, A
Pahuja, A
Lusis, AJ
Reynolds, WF
机构
[1] Sidney Kimmel Canc Ctr, San Diego, CA 92121 USA
[2] Univ Calif Los Angeles, Ctr Hlth Sci, Dept Med, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Ctr Hlth Sci, Dept Microbiol & Mol Genet, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Ctr Hlth Sci, Dept Human Genet, Los Angeles, CA 90024 USA
[5] Neurocrine Biosci, San Diego, CA 92121 USA
关键词
EAE/MS; autoimmunity; macrophages; transgenic/knockout; neuroimmunology;
D O I
10.1016/S0165-5728(00)00392-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
EAE is a demyelinating disease which serves as an animal model for multiple sclerosis (MS). Myeloperoxidase (MPO) has been implicated in MS through its presence in invading macrophages, and by association of a -463G/A promoter polymorphism with increased risk. Also, MPO at 17q23.1 is within a region identified in genome scans as a MS susceptibility locus. We here examine the incidence of EAE in MPO knockout (KO) mice. MPO is detected in invading macrophages in the CNS of wild-type mice, yet unexpectedly, MPO-KO mice have significantly increased incidence of EAE: Ninety percent of MPO-KO mice developed complete hind limb paralysis as compared to 33% of wildtype (WT) littermates (P<0.0001). This is the first evidence that MPO plays a significant role in EAE, consistent with its postulated role in MS. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 105
页数:9
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