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人T淋巴细胞系对髓鞘碱性蛋白的反应:显性表位与HLAⅡ类限制性分子的关联

Response of human T lymphocyte lines to myelin basic protein: association of dominant epitopes with HLA class II restriction molecules.

作者信息

Chou Y K, Vainiene M, Whitham R, Bourdette D, Chou C H, Hashim G, Offner H, Vandenbark A A

机构信息

Department of Neuroimmunology Research, Veterans Administration Medical Center, Portland, OR 97201.

出版信息

J Neurosci Res. 1989 Jun;23(2):207-16. doi: 10.1002/jnr.490230211.

Abstract

In animals, the selection in vitro of T cell lines to myelin basic protein (MBP) can define immunodominant and encephalitogenic epitopes which are preferentially associated with class II major histocompatibility (MHC) molecules. These principles were used to evaluate the specificity and MHC restriction of 14 human MBP-reactive T cell lines selected from normal individuals and patients with multiple sclerosis (MS) and other neurological diseases (OND). The four normal T cell lines recognized single, separate immunodominant MBP epitopes which were restricted by MHC molecules from the DR or in one case the DP class II locus. In contrast, the MS and OND T cell lines recognized multiple MBP epitopes, each in association with a discrete class II MHC molecule from the DR or DQ locus. Overall, HLA-DR molecules were used preferentially to associate with epitopes on human MBP, restricting 26/33 responses. As predicted from animal studies, T cells from genetically disparate individuals responded to different immunodominant epitopes on human MBP in association with distinct MHC class II molecules. HLA-DR2, which is overrepresented in MS patients, possessed an unusual capacity to restrict all eight epitopes identified on MBP in this study. These data provide the first evidence of genetically restricted human T cell recognition of potentially encephalitogenic epitopes of MBP.

摘要

在动物中,体外选择对髓鞘碱性蛋白(MBP)产生反应的T细胞系能够确定免疫显性和致脑炎性表位,这些表位优先与II类主要组织相容性(MHC)分子相关。这些原理被用于评估从正常个体、多发性硬化症(MS)患者及其他神经疾病(OND)患者中筛选出的14个人类MBP反应性T细胞系的特异性和MHC限制性。4个正常T细胞系识别单一、独立的免疫显性MBP表位,这些表位受来自DR或一例中受DP II类基因座的MHC分子限制。相比之下,MS和OND T细胞系识别多个MBP表位,每个表位都与来自DR或DQ基因座的离散II类MHC分子相关。总体而言,HLA-DR分子优先用于与人类MBP上的表位结合,限制了26/33的反应。正如动物研究预测的那样,来自遗传上不同个体的T细胞与不同的II类MHC分子结合,对人类MBP上不同的免疫显性表位产生反应。在MS患者中过度表达的HLA-DR2具有限制本研究中在MBP上鉴定出的所有8个表位的特殊能力。这些数据首次证明了人类T细胞对MBP潜在致脑炎性表位的遗传限制性识别。

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