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
相关论文
共 45 条
[31]  
RENNO T, 1995, J IMMUNOL, V154, P944
[32]   MPO and APOEε4 polymorphisms interact to increase risk for AD in Finnish males [J].
Reynolds, WF ;
Hiltunen, M ;
Pirskanen, M ;
Mannermaa, A ;
Helisalmi, S ;
Lehtovirta, M ;
Alafuzoff, I ;
Soininen, H .
NEUROLOGY, 2000, 55 (09) :1284-1290
[33]   Myeloperoxidase polymorphism is associated with gender specific risk for Alzheimer's disease [J].
Reynolds, WF ;
Rhees, J ;
Maciejewski, D ;
Paladino, T ;
Sieburg, H ;
Maki, RA ;
Masliah, E .
EXPERIMENTAL NEUROLOGY, 1999, 155 (01) :31-41
[34]   An allelic association implicates myeloperoxidase in the etiology of acute promyelocytic leukemia [J].
Reynolds, WF ;
Chang, E ;
Douer, D ;
Ball, ED ;
Kanda, V .
BLOOD, 1997, 90 (07) :2730-2737
[35]   AN ANTIBODY TO LYMPHOTOXIN AND TUMOR-NECROSIS-FACTOR PREVENTS TRANSFER OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS [J].
RUDDLE, NH ;
BERGMAN, CM ;
MCGRATH, KM ;
LINGENHELD, EG ;
GRUNNET, ML ;
PADULA, SJ ;
CLARK, RB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (04) :1193-1200
[36]  
Sahrbacher UC, 1998, EUR J IMMUNOL, V28, P1332, DOI 10.1002/(SICI)1521-4141(199804)28:04<1332::AID-IMMU1332>3.3.CO
[37]  
2-7
[38]   A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 [J].
Sawcer, S ;
Jones, HB ;
Feakes, R ;
Gray, J ;
Smaldon, N ;
Chataway, J ;
Robertson, N ;
Clayton, D ;
Goodfellow, PN ;
Compston, A .
NATURE GENETICS, 1996, 13 (04) :464-468
[39]   ASSOCIATION BETWEEN TUMOR-NECROSIS-FACTOR-ALPHA AND DISEASE PROGRESSION IN PATIENTS WITH MULTIPLE-SCLEROSIS [J].
SHARIEF, MK ;
HENTGES, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (07) :467-472
[40]   Increased severity of experimental autoimmune encephalomyelitis, chronic macrophage/microglial reactivity, and demyelination in transgenic mice producing tumor necrosis factor-alpha in the central nervous system [J].
Taupin, VR ;
Renno, T ;
Bourbonniere, L ;
Peterson, AC ;
Rodriguez, M ;
Owens, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (04) :905-913