The human CMV-UL86 peptide 981–1003 shares a crossreactive T-cell epitope with the encephalitogenic MOG peptide 34–56, but lacks the capacity to induce EAE in rhesus monkeys

Abstract Rhesus monkeys immunized with MOG34–56 , a dominant T-cell epitope from myelin/oligodendrocyte glycoprotein, develop an acute neurological disease resembling acute disseminated encephalomyelitis (ADEM) in humans. The typical large demyelinated lesions and mononuclear infiltrates in the monk...

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Veröffentlicht in:Journal of neuroimmunology 2007-01, Vol.182 (1), p.135-152
Hauptverfasser: Brok, Herbert P.M, Boven, Leonie, van Meurs, Marjan, Kerlero de Rosbo, Nicole, Celebi-Paul, Liesbeth, Kap, Yolanda S, Jagessar, Anwar, Hintzen, Rogier Q, Keir, Geoff, Bajramovic, Jeffrey, Ben-Nun, Avraham, Bauer, Jan, Laman, Jon D, Amor, Sandra, t Hart, Bert A
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Sprache:eng
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Zusammenfassung:Abstract Rhesus monkeys immunized with MOG34–56 , a dominant T-cell epitope from myelin/oligodendrocyte glycoprotein, develop an acute neurological disease resembling acute disseminated encephalomyelitis (ADEM) in humans. The typical large demyelinated lesions and mononuclear infiltrates in the monkey brains are caused by MOG34–56 T-cells. We show that MOG34–56 -reactive CD4+ and CD8+ T-cells are induced in monkeys immunized with a peptide from the human CMV major capsid protein (UL86; 981–1003), that shares sequence similarity with MOG34–56 . Monkeys sensitized against the viral peptide and subsequently challenged with MOG34–56 display histological signs of encephalitis, but do not show overt neurological signs.
ISSN:0165-5728
1872-8421
DOI:10.1016/j.jneuroim.2006.10.010