Kono D H, Urban J L, Horvath S J, Ando D G, Saavedra R A, Hood L
Division of Biology, California Institute of Technology, Pasadena 91125.
J Exp Med. 1988 Jul 1;168(1):213-27. doi: 10.1084/jem.168.1.213.
Experimental allergic encephalomyelitis (EAE) is an autoimmune demyelinating disease of the central nervous system (CNS) that occurs after immunization of animals with myelin basic protein (MBP). The disease is a prototype model for the study of antigen-specific T helper cell-mediated autoimmune disease. In SJL/J mice, EAE is mediated by T helper cells directed against a 40-amino acid COOH-terminal peptic fragment of mouse small MBP. To identify the minimal T cell epitopes of MBP responsible for EAE, overlapping peptides completely encompassing the epitopes within this region were synthesized. A 28-residue peptide of mouse MBP spanning residues 87-114 (pM87-114) was able to elicit both a strong T cell response and chronic relapsing disease. To better localize the T cell epitopes, shorter peptides within this region were synthesized and two overlapping peptides, pM87-98 and pM91-104, were able to induce EAE. T cell clones and bulk lymph node cell populations reactive with pM87-98 did not respond to pM91-104. However, lymph node cells reactive with pM91-104 also reacted with pM87-98, thus showing that these two peptides represent contiguous, but distinct encephalitogenic epitopes and that both these epitopes may be contained within pM87-98. In addition, pM87-114 and pM87-98 were found to be minor determinants of the total T cell response to rat and rabbit MBP. The restricted response to MBP in SJL/J mice is similar to that of the PL/J mice in that each appears to have only a single peptide region in MBP that elicits encephalitogenic T cells. However, within the region studied, there were two if not more T cell epitopes. This differs from the single encephalitogenic PL/J epitope. These findings of a single encephalitogenic peptide region with multiple T cell epitopes and the fact that encephalitogenic T cell epitopes may be subdominant have implications for the design of treatments directed at the T cell receptor-MHC-peptide epitope complex in autoimmune disease.
实验性变应性脑脊髓炎(EAE)是一种中枢神经系统(CNS)的自身免疫性脱髓鞘疾病,在动物用髓鞘碱性蛋白(MBP)免疫后发生。该疾病是研究抗原特异性T辅助细胞介导的自身免疫性疾病的原型模型。在SJL/J小鼠中,EAE由针对小鼠小MBP的40个氨基酸的COOH末端消化片段的T辅助细胞介导。为了确定负责EAE的MBP的最小T细胞表位,合成了完全包含该区域内表位的重叠肽。小鼠MBP的一个28个残基的肽段,跨越87-114位残基(pM87-114),能够引发强烈的T细胞反应和慢性复发性疾病。为了更好地定位T细胞表位,合成了该区域内较短的肽段,两个重叠肽段pM87-98和pM91-104能够诱导EAE。与pM87-98反应的T细胞克隆和大量淋巴结细胞群体对pM91-104无反应。然而,与pM91-104反应的淋巴结细胞也与pM87-98反应,因此表明这两个肽段代表连续但不同的致脑炎性表位,并且这两个表位可能都包含在pM87-98内。此外,发现pM87-114和pM87-98是对大鼠和兔MBP的总T细胞反应的次要决定因素。SJL/J小鼠对MBP的限制性反应与PL/J小鼠相似,即每只小鼠似乎在MBP中只有一个肽段区域能引发致脑炎性T细胞。然而,在所研究的区域内,有两个或更多的T细胞表位。这与单一的PL/J致脑炎性表位不同。这些关于单一致脑炎性肽段区域具有多个T细胞表位的发现以及致脑炎性T细胞表位可能是次要的这一事实,对自身免疫性疾病中针对T细胞受体-MHC-肽表位复合物的治疗设计具有重要意义。