Suppression of ongoing experimental allergic encephalomyelitis in DA rats by novel peptide drug, structural part of human myelin basic protein 46-62

被引:10
作者
Belogurov, A. A., Jr. [1 ,4 ]
Zargarova, T. A. [2 ]
Turobov, V. I. [2 ]
Novikova, N. I. [2 ]
Favorova, O. O. [3 ]
Ponomarenko, N. A. [1 ]
Gabibov, A. G. [1 ,4 ]
机构
[1] Russian Acad Sci, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[2] Russian Acad Sci, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Pushchino Branch, Pushchino 142290, Russia
[3] Cardiol Res Ctr, Inst Expt Cardiol, Moscow 121552, Russia
[4] Russian Acad Sci, Inst Gene Biol, Moscow 119334, Russia
关键词
Experimental allergic encephalomyelitis; myelin basic protein; multiple sclerosis; DA rats; Copaxone (R); EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ORAL GLATIRAMER ACETATE; MULTIPLE-SCLEROSIS; AUTOANTIBODIES; DEGRADATION;
D O I
10.1080/08916930902832090
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previously, we demonstrated that autoantibodies (AAb) in multiple sclerosis ( MS) reveal site-specific binding and cleavage toward myelin basic protein (MBP) epitope library. We have found several fragments of MBP immunodominant in terms of AAb binding. Here, we applied these peptides to DA rats with induced protracted relapsing experimental allergic encephalomyelitis (EAE) most closely related to MS. DA rats with EAE induced by syngenic spinal cord homogenate in complete Freund's adjuvant were treated by nasal route with human MBP 46-62, 81-102, 124-139, 147-170, and Copaxone (R). MBP 124-139 and 147-170 displayed only mild therapeutic effects but MBP 46-62 significantly reduced EAE, reflected by lower clinical scores and shorter EAE duration compared to controls.
引用
收藏
页码:362 / 364
页数:3
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