Screening of several H-2 congenic mouse strains identified H-2q mice as highly susceptible to MOG-induced EAE with minimal adjuvant requirement

被引:58
作者
Abdul-Majid, KB [1 ]
Jirholt, J
Stadelmann, C
Stefferl, A
Kjellén, P
Wallström, E
Holmdahl, R
Lassmann, H
Olsson, T
Harris, RA
机构
[1] Karolinska Hosp, Ctr Mol Med L8 04, Neuroimmunol Unit, SE-17176 Stockholm, Sweden
[2] Lund Univ, SE-22362 Lund, Sweden
[3] Univ Vienna, Brain Res Inst, A-1090 Vienna, Austria
关键词
EAE; MOG; H-2(q); DBA/1;
D O I
10.1016/S0165-5728(00)00360-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
We identified H-2(q) as a susceptible genotype for MOG-induced EAE by systematic screening of a series of H-2 congenic B10 mouse strains. A series of H-2(q)-bearing strains with divergent gene backgrounds were subsequently investigated. DBA/1 mice were highly susceptible to MOG(1-125)- and MOG(79-96)-induced EAE in the absence of pertussis toxin. Immunisation with MOG(1-125) and MOG(79-96) induced an autoreactive T-cell response in DBA/1 mice. Brain histopathology revealed T-cell and macrophage-infiltrated lesions with associated demyelination. The important features which make this an appropriate model of human disease are high sensitivity to MOG and dependence of an immunodominant peptide region homologous to that implicated in multiple sclerosis. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:23 / 33
页数:11
相关论文
共 54 条
[1]
PURIFICATION AND PARTIAL STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN [J].
AMIGUET, P ;
GARDINIER, MV ;
ZANETTA, JP ;
MATTHIEU, JM .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1676-1682
[2]
AMOR S, 1994, J IMMUNOL, V153, P4349
[3]
BenNun A, 1997, P ASSOC AM PHYSICIAN, V109, P120
[4]
Myelin oligodendrocyte glycoprotein: A novel candidate autoantigen in multiple sclerosis [J].
Bernard, CCA ;
Johns, TG ;
Slavin, A ;
Ichikawa, M ;
Ewing, C ;
Liu, J ;
Bettadapura, J .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1997, 75 (02) :77-88
[5]
Genetic analysis of the influence of pertussis toxin on experimental allergic encephalomyelitis susceptibility: An environmental agent can override genetic checkpoints [J].
Blankenhorn, EP ;
Butterfield, RJ ;
Rigby, R ;
Cort, L ;
Giambrone, D ;
McDermott, P ;
McEntee, K ;
Solowski, N ;
Meeker, ND ;
Zachary, JF ;
Doerge, RW ;
Teuscher, C .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :3420-3425
[6]
Epitope specificity of demyelinating monoclonal autoantibodies directed against the human myelin oligodendrocyte glycoprotein (MOG) [J].
Brehm, U ;
Piddlesden, SJ ;
Gardinier, MV ;
Linington, C .
JOURNAL OF NEUROIMMUNOLOGY, 1999, 97 (1-2) :9-15
[7]
IMMUNIZATION AGAINST HETEROLOGOUS TYPE-II COLLAGEN INDUCES ARTHRITIS IN MICE [J].
COURTENAY, JS ;
DALLMAN, MJ ;
DAYAN, AD ;
MARTIN, A ;
MOSEDALE, B .
NATURE, 1980, 283 (5748) :666-668
[8]
CHRONIC RELAPSING EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS WITH A DELAYED-ONSET AND AN ATYPICAL CLINICAL COURSE, INDUCED IN PL/J MICE BY MYELIN OLIGODENDROCYTE GLYCOPROTEIN (MOG)-DERIVED PEPTIDE - PRELIMINARY-ANALYSIS OF MOG T-CELL EPITOPES [J].
DEROSBO, NK ;
MENDEL, I ;
BENNUN, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (04) :985-993
[9]
QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing I/2 [J].
Encinas, JA ;
Wicker, LS ;
Peterson, LB ;
Mukasa, A ;
Teuscher, C ;
Sobel, R ;
Weiner, HL ;
Seidman, CE ;
Seidman, JG ;
Kuchroo, VK .
NATURE GENETICS, 1999, 21 (02) :158-160
[10]
Quantitative analysis of peptides from myelin basic protein binding to the MHC class II protein, I-A(u), which confers susceptibility to experimental allergic encephalomyelitis [J].
Fugger, L ;
Liang, J ;
Gautam, A ;
Rothbard, JB ;
McDevitt, HO .
MOLECULAR MEDICINE, 1996, 2 (02) :181-188