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
相关论文
共 41 条
  • [1] RESPONSE OF HUMAN LYMPHOCYTE-T LINES TO MYELIN BASIC-PROTEIN - ASSOCIATION OF DOMINANT EPITOPES WITH HLA CLASS-II RESTRICTION MOLECULES
    CHOU, YK
    VAINIENE, M
    WHITHAM, R
    BOURDETTE, D
    CHOU, CHJ
    HASHIM, G
    OFFNER, H
    VANDENBARK, AA
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 23 (02) : 207 - 216
  • [2] FREQUENCY OF T-CELLS SPECIFIC FOR MYELIN BASIC-PROTEIN AND MYELIN PROTEOLIPID PROTEIN IN BLOOD AND CEREBROSPINAL-FLUID IN MULTIPLE-SCLEROSIS
    CHOU, YK
    BOURDETTE, DN
    OFFNER, H
    WHITHAM, R
    WANG, RY
    HASHIM, GA
    VANDENBARK, AA
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1992, 38 (1-2) : 105 - 113
  • [3] COMPSTON A, 1986, P56
  • [4] SUSCEPTIBILITY TO PROTEOLIPID APOPROTEIN AND ITS ENCEPHALITOGENIC DETERMINANTS IN MICE
    ENDOH, M
    KUNISHITA, T
    NIHEI, J
    NISHIZAWA, M
    TABIRA, T
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1990, 92 (04): : 433 - 438
  • [5] HLAS AND GENES IN JAPANESE PATIENTS WITH MULTIPLE-SCLEROSIS - EVIDENCE FOR INCREASED FREQUENCIES OF HLA-CW3, HLA-DR2, AND HLA-DQB1-ASTERISK-0602
    HAO, Q
    SAIDA, T
    KAWAKAMI, H
    MINE, H
    MARUYA, E
    INOKO, H
    SAJI, H
    [J]. HUMAN IMMUNOLOGY, 1992, 35 (02) : 116 - 124
  • [6] THE HLA-DW2 HAPLOTYPE SEGREGATES CLOSELY WITH MULTIPLE-SCLEROSIS IN MULTIPLEX FAMILIES
    HILLERT, J
    KALL, T
    VRETHEM, M
    FREDRIKSON, S
    OHLSON, M
    OLERUP, O
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1994, 50 (01) : 95 - 100
  • [7] T-LYMPHOCYTE LINES AND CLONES SELECTED AGAINST SYNTHETIC MYELIN BASIC-PROTEIN 82-102 PEPTIDE FROM JAPANESE MULTIPLE-SCLEROSIS PATIENTS
    INOBE, J
    YAMAMURA, T
    KUNISHITA, T
    TABIRA, T
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1993, 46 (1-2) : 83 - 90
  • [8] INOBE J-I, 1992, Neurology, V42, P159
  • [9] THE T-CELL RESPONSE TO MYELIN BASIC-PROTEIN IN FAMILIAL MULTIPLE-SCLEROSIS - DIVERSITY OF FINE SPECIFICITY, RESTRICTING ELEMENTS, AND T-CELL RECEPTOR USAGE
    JOSHI, N
    USUKU, K
    HAUSER, SL
    [J]. ANNALS OF NEUROLOGY, 1993, 34 (03) : 385 - 393
  • [10] EXPRESSION OF MYELIN PROTEINS IN THE DEVELOPING HUMAN SPINAL-CORD - CLONING AND SEQUENCING OF HUMAN PROTEOLIPID PROTEIN CDNA
    KRONQUIST, KE
    CRANDALL, BF
    MACKLIN, WB
    CAMPAGNONI, AT
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 1987, 18 (03) : 395 - 401