T cell recognition of myelin proteolipid protein and myelin proteolipid protein peptides in the peripheral blood of multiple sclerosis and control subjects

被引:58
作者
Trotter, JL
Pelfrey, CM
Trotter, AL
Selvidge, JA
Gushleff, KC
Mohanakumar, T
McFarland, HF
机构
[1] Washington Univ, Sch Med, Dept Neurol & Neurol Surg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[3] NINDS, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
关键词
multiple sclerosis; T cells; myelin proteolipid protein;
D O I
10.1016/S0165-5728(97)00260-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myelin proteolipid protein (PLP) is a prime candidate autoantigen for multiple sclerosis. In order to define potential immunodominant epitopes, T cell lines (TCL) from the peripheral blood of HLA-DR 15(2) MS patients were established which responded to the intact molecule of PLP. These TCL were then tested in individual proliferation assays with a variety of PLP peptides spanning most of the PLP molecule. Multiple peptides were recognized by TCL from the RIS population, with more than one peptide often recognized by lines from the same individual. Three immunodominant peptides were identified which were recognized by the majority of MS patients. Estimated frequency analyses were then performed on the peripheral blood of HLA-DR15(2)-positive MS and control subjects using TCL initiated by the three immunodominant peptides, 40-60, 95-117, and 185-206. TCL from HLA-DRIS MS subjects recognized peptide 95-117 significantly mon often than TCL from control subjects. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:172 / 178
页数:7
相关论文
共 58 条
[1]   LIMITED HETEROGENEITY OF T-CELL RECEPTORS FROM LYMPHOCYTES MEDIATING AUTOIMMUNE ENCEPHALOMYELITIS ALLOWS SPECIFIC IMMUNE INTERVENTION [J].
ACHAORBEA, H ;
MITCHELL, DJ ;
TIMMERMANN, L ;
WRAITH, DC ;
TAUSCH, GS ;
WALDOR, MK ;
ZAMVIL, SS ;
MCDEVITT, HO ;
STEINMAN, L .
CELL, 1988, 54 (02) :263-273
[2]   T-CELLS RESPONSIVE TO MYELIN BASIC-PROTEIN IN PATIENTS WITH MULTIPLE-SCLEROSIS [J].
ALLEGRETTA, M ;
NICKLAS, JA ;
SRIRAM, S ;
ALBERTINI, RJ .
SCIENCE, 1990, 247 (4943) :718-721
[3]  
AMOR S, 1993, J IMMUNOL, V150, P5666
[4]   FREQUENCY OF T-CELLS SPECIFIC FOR MYELIN BASIC-PROTEIN AND MYELIN PROTEOLIPID PROTEIN IN BLOOD AND CEREBROSPINAL-FLUID IN MULTIPLE-SCLEROSIS [J].
CHOU, YK ;
BOURDETTE, DN ;
OFFNER, H ;
WHITHAM, R ;
WANG, RY ;
HASHIM, GA ;
VANDENBARK, AA .
JOURNAL OF NEUROIMMUNOLOGY, 1992, 38 (1-2) :105-113
[5]   DEVELOPMENT OF REACTIVITY TO NEW MYELIN ANTIGENS DURING CHRONIC RELAPSING AUTOIMMUNE DEMYELINATION [J].
CROSS, AH ;
TUOHY, VK ;
RAINE, CS .
CELLULAR IMMUNOLOGY, 1993, 146 (02) :261-269
[6]  
CROSS AH, 1990, LAB INVEST, V63, P162
[7]   Induction of EAE in mice with recombinant human MOG, and treatment of EAE with a MOG peptide [J].
Devaux, B ;
Enderlin, F ;
Wallner, B ;
Smilek, DE .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 75 (1-2) :169-173
[8]   INDIVIDUAL EXONS ENCODE THE INTEGRAL MEMBRANE DOMAINS OF HUMAN MYELIN PROTEOLIPID PROTEIN [J].
DIEHL, HJ ;
SCHAICH, M ;
BUDZINSKI, RM ;
STOFFEL, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9807-9811
[9]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[10]   AMELIORATION OF AUTOIMMUNE ENCEPHALOMYELITIS BY MYELIN BASIC-PROTEIN SYNTHETIC PEPTIDE INDUCED ANERGY [J].
GAUR, A ;
WIERS, B ;
LIU, A ;
ROTHBARD, J ;
FATHMAN, CG .
SCIENCE, 1992, 258 (5087) :1491-1494