作者
George Deraos, Maria Rodi, Hubert Kalbacher, Kokona Chatzantoni, Fotios Karagiannis, Loukas Synodinos, Panayiotis Plotas, Apostolos Papalois, Nikolaos Dimisianos, Panagiotis Papathanasopoulos, Dimitrios Gatos, Theodore Tselios, Vasso Apostolopoulos, Athanasia Mouzaki, John Matsoukas
发表日期
2015/8/28
期刊
European journal of medicinal chemistry
卷号
101
页码范围
13-23
出版商
Elsevier Masson
简介
Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the central nervous system, and it has been established that autoreactive T helper (Th) cells play a crucial role in its pathogenesis. Myelin basic protein (MBP) epitopes are major autoantigens in MS, and the sequence MBP87-99 is an immunodominant epitope. We have previously reported that MBP87-99 peptides with modifications at principal T-cell receptor (TCR) contact sites suppressed the induction of EAE symptoms in rats and SJL/J mice, diverted the immune response from Th1 to Th2 and generated antibodies that did not cross react with the native MBP protein. In this study, the linear and cyclic analogs of the MBP87-99 epitope, namely linear (Ala91,Ala96)MBP87-99 (P2) and cyclo(87-99)(Ala91,Ala96)MBP87-99 (P3), were evaluated for their binding to HLA-DR4, stability to lysosomal enzymes, their effect on cytokine secretion by …
引用总数
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