Sun D, Gold D P, Smith L, Brostoff S, Coleclough C
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38101.
Eur J Immunol. 1992 Feb;22(2):591-4. doi: 10.1002/eji.1830220244.
In this study, we demonstrate that T cell lines specific for a synthetic peptide representing sequence 87 to 99 of myelin basic protein (MBP) are encephalitogenic in Lewis rats. However, unlike syngeneic T cells specific for MBP residues 68 to 88 which exclusively use V beta 8 in their antigen receptors, these cells do not. None of the 10 T cell lines and T hybridomas specific for MBP (87-99) used V beta 8 in their T cell receptors. Our results document for the first time that rat encephalitogenic T cells do not exclusively use V beta 8 in T cell receptors that rat encephalitogenic T cells specific for MBP (87-99) are heterogeneous and that MBP (87-99) contains at least two epitopes for rat T cells.
在本研究中,我们证明,对代表髓鞘碱性蛋白(MBP)第87至99位序列的合成肽具有特异性的T细胞系在Lewis大鼠中具有致脑炎性。然而,与对MBP第68至88位残基具有特异性的同基因T细胞不同,后者在其抗原受体中仅使用Vβ8,而这些细胞并非如此。10个对MBP(87 - 99)具有特异性的T细胞系和T杂交瘤中,没有一个在其T细胞受体中使用Vβ8。我们的结果首次证明,大鼠致脑炎性T细胞在T细胞受体中并非仅使用Vβ8,对MBP(87 - 99)具有特异性的大鼠致脑炎性T细胞是异质性的,并且MBP(87 - 99)包含至少两个针对大鼠T细胞的表位。