ANALYSIS OF PROTEOLIPID PROTEIN (PLP)-SPECIFIC T-CELLS IN MULTIPLE-SCLEROSIS - IDENTIFICATION OF PLP-95-116 AS AN HLA-DR2,W15-ASSOCIATED DETERMINANT

被引:38
作者
OHASHI, T [1 ]
YAMAMURA, T [1 ]
INOBE, J [1 ]
KONDO, T [1 ]
KUNISHITA, T [1 ]
TABIRA, T [1 ]
机构
[1] NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT DEMYELINATING DIS & AGING,KODAIRA,TOKYO 187,JAPAN
基金
日本科学技术振兴机构;
关键词
AUTOIMMUNE T CELLS; HLA-DR2; MULTIPLE SCLEROSIS; PROTEOLIPID PROTEIN; T CELL EPITOPE;
D O I
10.1093/intimm/7.11.1771
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is a putative autoimmune disease that is linked with HLA-DR2,w15. Proteolipid protein (PLP) is a candidate autoantigen in MS, but the disease-associated epitopes have not been determined, Using overlapping and non-overlapping PLP peptides, we have studied the T cell response to the major hydrophilic domain PLP 85-159 in the peripheral blood of MS and healthy subjects (HS), Short-term T cell lines (TCL) were selected against each peptide using microwell plates and the frequency of peptide-specific TCL was estimated, PLP 95-116-specific TCL were most efficiently generated and the frequency was significantly higher in MS compared with HS (P < 0.05), When compared between DR2,w15(+) and DR2,w15(-) MS, TCL frequency to PLP 95-116 was significantly higher in DR2,w15(+) MS (P < 0.005) and TCL reactive to the overlapping peptide 105-124 were also increased in DR2,w15(+) MS (P < 0.025), Using DR gene-transfected L cells, we could show that the DRB1*1501 product of the DR2 haplotype presents PLP 95-116 to TCL selected against the peptide, These results imply that PLP 95-116 represents a major epitope for the DR2,w15(+) MS.
引用
收藏
页码:1771 / 1778
页数:8
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