Topham D J, Nag B, Arimilli S, Sriram S
Department of Neurology, Vanderbilt University, Vanderbilt-Stallworth, Hospital, Nashville, TN 37212.
Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8005-9. doi: 10.1073/pnas.91.17.8005.
Experimental autoimmune encephalomyelitis (EAE) is a class II major histocompatibility complex (MHC)-restricted, T-cell-mediated, demyelinating autoimmune disease of the central nervous system and represents a model for human multiple sclerosis. The present study demonstrates that vaccination of SJL/J mice with an 18-amino acid synthetic peptide from the third hypervariable region of the murine class II MHC IAs beta chain (IAs beta 58-75; 18-mer peptide) is capable of eliciting auto-anti-IAs antibodies specific for the IAs beta chain and preventing and treating EAE. A similar approach may be useful in the treatment of human autoimmune diseases in which susceptibility is linked to class II MHC genes.
实验性自身免疫性脑脊髓炎(EAE)是一种II类主要组织相容性复合体(MHC)限制的、T细胞介导的中枢神经系统脱髓鞘自身免疫性疾病,是人类多发性硬化症的模型。本研究表明,用来自小鼠II类MHC IAsβ链第三高变区的18个氨基酸合成肽(IAsβ58 - 75;18肽)对SJL/J小鼠进行疫苗接种,能够引发针对IAsβ链的自身抗IAs抗体,并预防和治疗EAE。类似的方法可能对治疗易感性与II类MHC基因相关的人类自身免疫性疾病有用。