ABNORMAL T-CELL EXPANSION AND V-GENE USAGE IN MYASTHENIA-GRAVIS PATIENTS

被引:38
作者
GRUNEWALD, J
AHLBERG, R
LEFVERT, AK
DERSIMONIAN, H
WIGZELL, H
JANSON, CH
机构
[1] KAROLINSKA HOSP,S-10401 STOCKHOLM 60,SWEDEN
[2] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,IMMUNOCHEM LAB,BOSTON,MA 02115
关键词
D O I
10.1111/j.1365-3083.1991.tb01533.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To determine the extent of V-gene heterogeneity of blood T lymphocytes in patients suffering from Myasthenia Gravis (MG), we used eight recently available monoclonal antibodies (MoAb), directed against different V-alpha and V-beta gene products of the variable part of the T-cell receptor (TCR), covering approximately 25% of the alpha/beta T cells in normal peripheral blood (PBL) of healthy individuals. Using a two-colour immunofluorescence method, we could calculate the expression of alpha/beta-V segments within the two major T-cell subsets, CD4-/CD8+ and CD4+/CD8- lymphocytes. Twenty-seven per cent (4/15) of the MG patients had T cells showing signs of abnormal expansion. Furthermore, among these expanded T cells, a restricted V-beta-12 gene expansion could be seen, in three out of four patients. No correlation between TCR V-gene usage and HLA haplotypes (HLA-A, -B, -DR and -DQ) could be seen. Our data suggest that the majority of MG patients have abnormally expanded T-cell clones. The relevance of these findings is discussed.
引用
收藏
页码:161 / 168
页数:8
相关论文
共 33 条
  • [1] LIMITED HETEROGENEITY OF T-CELL RECEPTORS FROM LYMPHOCYTES MEDIATING AUTOIMMUNE ENCEPHALOMYELITIS ALLOWS SPECIFIC IMMUNE INTERVENTION
    ACHAORBEA, H
    MITCHELL, DJ
    TIMMERMANN, L
    WRAITH, DC
    TAUSCH, GS
    WALDOR, MK
    ZAMVIL, SS
    MCDEVITT, HO
    STEINMAN, L
    [J]. CELL, 1988, 54 (02) : 263 - 273
  • [2] AHLBERG R, IN PRESS CLIN IMMUNO
  • [3] DETECTION OF A FREQUENT RESTRICTION FRAGMENT LENGTH POLYMORPHISM IN THE HUMAN T-CELL ANTIGEN RECEPTOR BETA-CHAIN LOCUS - A POTENTIAL DIAGNOSTIC-TOOL
    BERLINER, N
    DUBY, AD
    MORTON, CC
    LEDER, P
    SEIDMAN, JG
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (03) : 1283 - 1285
  • [4] BIGLER R, 1983, J EXP MED, V150, P1000
  • [5] BOYLSTON AW, 1986, J IMMUNOL, V137, P741
  • [6] BRENNAN FM, 1988, CLIN EXP IMMUNOL, V73, P417
  • [7] DIFFERENT HLA DR-DQ ASSOCIATIONS IN SUBGROUPS OF IDIOPATHIC MYASTHENIA-GRAVIS
    CARLSSON, B
    WALLIN, J
    PIRSKANEN, R
    MATELL, G
    SMITH, CIE
    [J]. IMMUNOGENETICS, 1990, 31 (5-6) : 285 - 290
  • [8] EVIDENCE OF ENHANCED RECOMBINANT INTERLEUKIN-2 SENSITIVITY IN THYMIC LYMPHOCYTES FROM PATIENTS WITH MYASTHENIA-GRAVIS - POSSIBLE ROLE IN AUTOIMMUNE PATHOGENESIS
    COHENKAMINSKY, S
    LEVASSEUR, P
    BINET, JP
    BERRIH-AKNIN, S
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1989, 24 (1-2) : 75 - 85
  • [9] HIGH RECOMBINANT INTERLEUKIN-2 SENSITIVITY OF PERIPHERAL-BLOOD LYMPHOCYTES FROM PATIENTS WITH MYASTHENIA-GRAVIS - CORRELATIONS WITH CLINICAL-PARAMETERS
    COHENKAMINSKY, S
    GAUD, C
    MOREL, E
    BERRIH-AKNIN, S
    [J]. JOURNAL OF AUTOIMMUNITY, 1989, 2 (03) : 241 - 258
  • [10] T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION
    DAVIS, MM
    BJORKMAN, PJ
    [J]. NATURE, 1988, 334 (6181) : 395 - 402