PATTERNS OF CD16 AND CD56 EXPRESSION IN PERSISTENT EXPANSIONS OF CD3+NKA+ LYMPHOCYTES ARE PREDICTIVE FOR CLONAL T-CELL RECEPTOR GENE REARRANGEMENTS

被引:16
作者
SIVAKUMARAN, M
RICHARDS, SJ
HUNT, KM
STEED, AJ
BYNOE, AG
MORGAN, MM
PYRAH, R
ROBERTS, BE
SCOTT, CS
机构
[1] COOKRIDGE HOSP,DEPT HAEMATOL,LEUKAEMIA DIAGNOST UNIT,LEEDS LS16 6QB,W YORKSHIRE,ENGLAND
[2] GEN INFIRM,LEEDS LS1 3EX,W YORKSHIRE,ENGLAND
[3] COOKRIDGE HOSP,MOLEC HEMATOL UNIT,LEEDS LS16 6QB,W YORKSHIRE,ENGLAND
关键词
D O I
10.1111/j.1365-2141.1991.tb04450.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Phenotypic characteristics, and correlations between the expression of membrane NK-associated (NKa) determinants (CD11b, CD16, CD56 and CD57) and T cell receptor (TCR) genotypic patterns, were examined in 25 patients with persistent (> 6 months) expansions of CD3+WT31+NKa+ (CD8+ and CD8dim+) lymphocytes. These studies showed that distinct NKa phenotypic profiles were restricted to cases with rearranged TCR configurations and that clonal CD3+NKa+ components could be predicted in most cases by assessing relationships between membrane CD16 and CD56 expression. For all normal NKa subpopulations, there was a high correlation (P < 0.0001; n = 31) between the expression of these two membrane determinants. Markedly increased CD16 expression by CD3+NKa+ cells, in relation to CD56 (i.e. a high CD16:CD56 ratio), was found exclusively in cases with rearranged TCR (13/16 cases): 2/3 of the remaining cases showing significantly reduced CD16:CD56 ratios and high (> 2.0) CD3+ CD56+ absolute numbers. In contrast, 7/9 of the germline TCR cases had a normal CD16:CD56 ratio and 2/9 a decreased ratio with low (> 1.0) CD3+ CD56+ absolute numbers. A high ratio of CD16:CD56 expression by CD3+ NKa+ lymphocytes was therefore informative for 82% of TCR rearrangements in this series; and analysis of CD16 and CD56 expression was predictive for germline and rearranged TCR configurations in 24/25 persistent CD3+ NKa+ expansions.
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页码:368 / 377
页数:10
相关论文
共 12 条
[1]   RHEUMATOID-ARTHRITIS ASSOCIATED WITH EXPANDED POPULATIONS OF ANTIGRANULOCYTES LYMPHOCYTES [J].
BARTON, JC ;
PRASTHOFER, EF ;
EGAN, ML ;
HECK, LW ;
KOOPMAN, WJ ;
GROSSI, CE .
ANNALS OF INTERNAL MEDICINE, 1986, 104 (03) :314-323
[2]  
FORONI L, 1988, BLOOD, V71, P356
[3]   DOES OCCULT MONOCLONAL PROLIFERATION OF NON-MALIGNANT T-CELLS CAUSE SECONDARY IMMUNOPATHOLOGICAL DISORDERS [J].
GOUDIE, RB ;
LEE, FD .
JOURNAL OF PATHOLOGY, 1989, 158 (02) :91-92
[4]   IS RHEUMATOID-ARTHRITIS REALLY A CONSEQUENCE OF BENIGN T-CELL NEOPLASIA [J].
GOUDIE, RB ;
LEE, FD .
JOURNAL OF PATHOLOGY, 1990, 160 (01) :3-3
[5]  
LOUGHRAN TP, 1988, BLOOD, V71, P822
[6]   LARGE ANTIGRANULOCYTES LYMPHOCYTE LEUKEMIA - REPORT OF 38 CASES AND REVIEW OF THE LITERATURE [J].
LOUGHRAN, TP ;
STARKEBAUM, G .
MEDICINE, 1987, 66 (05) :397-405
[7]  
NEWLAND AC, 1984, BRIT J HAEMATOL, V58, P443
[8]  
PANDOLFI F, 1986, DIAGN CLIN IMMUNOL, V4, P61
[9]   T-CELL RECEPTOR BETA-CHAIN GENE REARRANGEMENTS IN LYMPHOPROLIFERATIVE DISORDERS OF LARGE GRANULAR LYMPHOCYTES - NATURAL-KILLER CELLS [J].
RAMBALDI, A ;
PELICCI, PG ;
ALLAVENA, P ;
KNOWLES, DM ;
ROSSINI, S ;
BASSAN, R ;
BARBUI, T ;
DALLAFAVERA, R ;
MANTOVANI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (06) :2156-2162
[10]  
Richards S J, 1990, Leuk Lymphoma, V2, P111, DOI 10.3109/10428199009042521