Sun D, Hu X Z, Le J, Swanborg R H
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38101.
Eur J Immunol. 1994 Jun;24(6):1359-64. doi: 10.1002/eji.1830240618.
In the present study, we have isolated and characterized five myelin basic protein (MBP)-reactive T cell lines directly from the brains of Lewis rats during the early paralytic phase of experimental autoimmune encephalomyelitis (EAE). Each T cell line responded to the dominant encephalitogenic epitope spanning residues 68-88, and did not react against the conserved encephalitogenic epitope [MBP(87-99)] or the nonencephalitogenic MBP epitope [MBP(50-69)]. We determined the T cell receptor (TcR) beta chain usage by polymerase chain reaction, DNA sequencing analysis and by generation of MBP-reactive hybridomas from one of the T cell lines (BT74). The results revealed that brain-infiltrating, MBP-reactive T cells freshly isolated early in the course of the disease exhibit TcR diversity.
在本研究中,我们直接从实验性自身免疫性脑脊髓炎(EAE)早期麻痹阶段的Lewis大鼠脑中分离并鉴定了五条髓鞘碱性蛋白(MBP)反应性T细胞系。每条T细胞系对跨越68 - 88位氨基酸残基的主要致脑炎性表位有反应,而对保守的致脑炎性表位[MBP(87 - 99)]或非致脑炎性MBP表位[MBP(50 - 69)]无反应。我们通过聚合酶链反应、DNA测序分析以及从其中一条T细胞系(BT74)产生MBP反应性杂交瘤来确定T细胞受体(TcR)β链的使用情况。结果显示,在疾病过程早期新鲜分离的脑内浸润性MBP反应性T细胞表现出TcR多样性。