Myelin/oligodendrocyte glycoprotein-induced autoimmune encephalomyelitis in common marmosets: The encephalitogenic T cell epitope pMOG24-36 is presented by a monomorphic MHC class II molecule

被引:93
|
作者
Brok, HPM
Uccelli, A
de Rosbo, NK
Bontrop, RE
Roccatagliata, L
de Groot, NG
Capello, E
Laman, JD
Nicolay, K
Mancardi, GL
Ben-Nun, A
't Hart, BA
机构
[1] Biomed Primate Res Ctr, Dept Immunobiol, NL-2288 GJ Rijswijk, Netherlands
[2] Univ Genoa, Dept Neurol Sci, Genoa, Italy
[3] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[4] Erasmus Univ, Dept Immunol, Rotterdam, Netherlands
[5] Univ Utrecht, Dept Expt In Vivo NMR, Image Sci Inst, Utrecht, Netherlands
来源
JOURNAL OF IMMUNOLOGY | 2000年 / 165卷 / 02期
关键词
D O I
10.4049/jimmunol.165.2.1093
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunization of common marmosets (Callithrix jacchus) with a single dose of human myelin in CFA, without administration of Bordetella pertussis, induces a form of autoimmune encephalomyelitis (EAE) resembling in its clinical and pathological expression multiple sclerosis in humans. The EAE incidence in our outbred marmoset colony is 100%, This study was undertaken to assess the genetic and immunological basis of the high EAE susceptibility. To this end, we determined the separate contributions of immune reactions to myelin/oligodendrocyte glycoprotein (MOG) and myelin basic protein to the EAE induction. Essentially all pathological features of myelin-induced EAE were also found in animals immunized with MOG in CFA, whereas in animals immunized with myelin basic protein in CFA clinical and pathological signs of EAE were lacking, The epitope recognition by anti-MOG Abs and T cells were assessed. Evidence is provided that the initiation of EAE is based on T and B cell activation by the encephalitogenic phMOG14-36 peptide in the context of monomorphic Caja-DRB*W1201 molecules.
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收藏
页码:1093 / 1101
页数:9
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