Oligoclonality of CD8+ T cells in multiple sclerosis

被引:40
作者
Monteiro, J [1 ]
Hingorani, R [1 ]
Peroglizzi, R [1 ]
Apatoff, B [1 ]
Gregersen, PK [1 ]
机构
[1] N SHORE UNIV HOSP,CORNELL UNIV MED CTR,DEPT MED,MANHASSET,NY 11030
关键词
oligoclonality; CD8+ T lymphocytes; multiple sclerosis; T cell receptor repertoire;
D O I
10.3109/08916939608995336
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have shown earlier that CD8+ T cell oligoclonality occurs frequently in normal individuals and generally exhibits a very diverse repertoire, In order to investigate the role of CD8+ T cells in MS, we analysed CD8 olgoclonality in 125 patients with MS in varying stages of disease. A multiplex PCR assay for CDR3 length variation was employed to detect oligoclonality in 25 TCRBV segments/families. CD8 clonal dominance was found to be frequent in MS, Comparison of the CD8 T cell repertoire in MS with that in normal controls revealed an increased frequency of oligoclonality involving the TCRBV9, -18 and -23 families, Sequence analysis of the TCRs from these clonally dominant CD8+ cells revealed a high degree of diversity overall, However, we observed one instance of identical TCRBV18 sequences in CD8 cells from two unrelated MS patients, In addition, several TCRs with motifs homologous to those found in MS brain and MBP specific T cell clones in EAE and MS were also detected, Future characterization of the function and specificity of these clonally expanded populations may provide insight into the nature of immune dysregulation in this autoimmune disorder.
引用
收藏
页码:127 / 138
页数:12
相关论文
共 29 条
[1]   HOMOLOGIES BETWEEN T-CELL RECEPTOR JUNCTIONAL SEQUENCES UNIQUE TO MULTIPLE-SCLEROSIS AND T-CELLS MEDIATING EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS [J].
ALLEGRETTA, M ;
ALBERTINI, RJ ;
HOWELL, MD ;
SMITH, LR ;
MARTIN, R ;
MCFARLAND, HF ;
SRIRAM, S ;
BROSTOFF, S ;
STEINMAN, L .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :105-109
[2]  
Behar Samuel M., 1994, Arthritis and Rheumatism, V37, pS313
[3]  
BOURDETTE DN, 1994, J IMMUNOL, V152, P2510
[4]  
CHOU YK, 1994, J IMMUNOL, V152, P2520
[5]   SPECIFICITY OF HUMAN T-CELL CLONES REACTIVE TO IMMUNODOMINANT EPITOPES OF MYELIN BASIC-PROTEIN [J].
CHOU, YK ;
HENDERIKX, P ;
VAINIENE, M ;
WHITHAM, R ;
BOURDETTE, D ;
CHOU, CHJ ;
HASHIM, G ;
OFFNER, H ;
VANDENBARK, AA .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 28 (02) :280-290
[6]   CLONAL V-ALPHA-12.1+ T-CELL EXPANSIONS IN THE PERIPHERAL-BLOOD OF RHEUMATOID-ARTHRITIS PATIENTS [J].
DERSIMONIAN, H ;
SUGITA, M ;
GLASS, DN ;
MAIER, AL ;
WEINBLATT, ME ;
REME, T ;
BRENNER, MB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (06) :1623-1631
[7]   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
[8]   REQUIREMENT FOR CD8+ CELLS IN T-CELL RECEPTOR PEPTIDE-INDUCED CLONAL UNRESPONSIVENESS [J].
GAUR, A ;
HASPEL, R ;
MAYER, JP ;
FATHMAN, CG .
SCIENCE, 1993, 259 (5091) :91-94
[9]  
GOLD DP, 1992, J IMMUNOL, V148, P1712
[10]  
GRUNEWALD J, 1992, CLIN EXP IMMUNOL, V89, P279