Rajan A J, Cross A H, Raine C S, Diamond B
Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461.
Cell Immunol. 1993 Apr 1;147(2):378-87. doi: 10.1006/cimm.1993.1077.
Experimental allergic encephalomyelitis (EAE) is an autoimmune disease of the central nervous system. It is mediated by T cells and is an animal model for the human disease multiple sclerosis. In most mouse strains that are susceptible to induction of EAE by myelin basic protein, a dominant peptide of myelin basic protein is recognized by encephalitogenic T cells. We report here the susceptibility of the A.CA strain (H-2f) to myelin basic protein induced EAE and that multiple peptides of myelin basic protein (1-11, 9-20, and 87-99) can induce disease in these mice. The finding that multiple epitopes of the same self-antigen can elicit EAE in an inbred strain of mouse raises the possibility of more heterogeneity in encephalitogenic peptides of the putative autoantigen in human disease than previous studies have suggested.
实验性过敏性脑脊髓炎(EAE)是一种中枢神经系统的自身免疫性疾病。它由T细胞介导,是人类疾病多发性硬化症的动物模型。在大多数易被髓鞘碱性蛋白诱导发生EAE的小鼠品系中,致脑炎T细胞可识别髓鞘碱性蛋白的一种显性肽段。我们在此报告A.CA品系(H-2f)对髓鞘碱性蛋白诱导的EAE的易感性,以及髓鞘碱性蛋白的多种肽段(1-11、9-20和87-99)可在这些小鼠中诱发疾病。同一自身抗原的多个表位可在近交系小鼠中引发EAE这一发现,提示人类疾病中假定自身抗原的致脑炎肽段可能比以往研究所表明的更具异质性。