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CD3⁺NKa⁺淋巴细胞持续扩增中CD16和CD56的表达模式可预测克隆性T细胞受体基因重排。约克郡白血病研究小组。

Patterns of CD16 and CD56 expression in persistent expansions of CD3+NKa+ lymphocytes are predictive for clonal T-cell receptor gene rearrangements. The Yorkshire Leukaemia Group.

作者信息

Sivakumaran M, Richards S J, Hunt K M, Steed A J, Bynoe A G, Morgan M M, Pyrah R, Roberts B E, Scott C S

机构信息

Leukaemia Diagnostic Unit, Cookridge Hospital, Leeds.

出版信息

Br J Haematol. 1991 Jul;78(3):368-77. doi: 10.1111/j.1365-2141.1991.tb04450.x.

Abstract

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 (greater than 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 less than 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 (greater than 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 (less than 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.

摘要

对25例CD3+WT31+NKa+(CD8+和CD8dim+)淋巴细胞持续(超过6个月)扩增的患者,研究了其表型特征以及膜NK相关(NKa)决定簇(CD11b、CD16、CD56和CD57)表达与T细胞受体(TCR)基因型模式之间的相关性。这些研究表明,不同的NKa表型谱仅限于TCR构型重排的病例,并且在大多数情况下,通过评估膜CD16和CD56表达之间的关系,可以预测克隆性CD3+NKa+成分。对于所有正常的NKa亚群,这两种膜决定簇的表达之间存在高度相关性(P小于0.0001;n = 31)。仅在TCR重排的病例中(13/16例)发现CD3+NKa+细胞相对于CD56的CD16表达明显增加(即高CD16:CD56比值);其余病例中有2/3显示CD16:CD56比值显著降低且CD3+CD56+绝对数量较高(大于2.0)。相比之下,种系TCR病例中有7/9的CD16:CD56比值正常,2/9的比值降低且CD3+CD56+绝对数量较低(小于1.0)。因此,CD3+NKa+淋巴细胞的CD16:CD56高表达比值对该系列中82% 的TCR重排具有参考价值;并且对24/25例持续性CD3+NKa+扩增病例中,CD16和CD56表达的分析可预测种系和重排的TCR构型。

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