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首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >Circulating CD4+T lymphocytes with intracellular but no surface CD3 antigen in live of seven patients consecutively diagnosed with angioimmunoblastic T-cell lymphoma
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Circulating CD4+T lymphocytes with intracellular but no surface CD3 antigen in live of seven patients consecutively diagnosed with angioimmunoblastic T-cell lymphoma

机译:连续被诊断为血管免疫母细胞性T细胞淋巴瘤的七名患者的体内循环中具有细胞内但表面无CD3抗原的CD4 + T淋巴细胞

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摘要

Angioimmunoblastic T-cell lymphoma (AITL) accounts far less than 1% of all lymphatic malignancies. Oligoclonality or monoclonality for any of the T-cell receptor (TCR) chain genes can be demonstrated in the majority of the cases. During systematic screening for the presence of circulating lymphocytes with atypical coexpression of differentiation antigens in patients with T-cell lymphomas, we have discovered a minor population (accounting for 0.2% to 10% of all lymphocytes) of atypical lymphocytes in the blood of five of seven patients consecutively diagnosed in 1997/1998 by lymph node histology to have AITL. The major distinguishing feature of these cells consists of the lack of the surface expression of the CD3 antigen, but not of the intracellular expression. These cells express the T-cell antigens CD2 and CD5 on their surface, but not CD7, and they express CD4 and CD45 at numbers of molecules per cell typical for T lymphocytes. Gene scan analyses far the TCR gamma chain revealed oligoclonality of these flow-sorted cells in one patient and monoclonality in two patients, the same patterns of TCR gamma chain gene as determined processing the respective diagnostic lymph nodes. Circulating CD4-expressing T lymphocytes with exclusively cytoplasmic expression of CD3 appear to represent the malignant population in patients with histologically diagnosed AITL. Cytometry (Comm. Clin. Cytometry) 42:180-187, 2000. (C) 2000 Wiley-Liss, Inc. [References: 28]
机译:血管免疫母细胞性T细胞淋巴瘤(AITL)远少于所有淋巴恶性肿瘤的1%。在大多数情况下,都可以证明任何T细胞受体(TCR)链基因的寡聚或单克隆。在系统性筛查T细胞淋巴瘤患者中非典型分化抗原共表达的循环淋巴细胞的过程中,我们发现五分之一的血液中有一小部分非典型淋巴细胞(占所有淋巴细胞的0.2%至10%)。 1997/1998年经淋巴结组织学连续诊断为AITL的7例患者。这些细胞的主要区别特征在于缺乏CD3抗原的表面表达,而不是细胞内表达。这些细胞在其表面表达T细胞抗原CD2和CD5,而不在CD7上表达,并且它们以T细胞典型的每细胞分子数量表达CD4和CD45。对TCRγ链进行的基因扫描分析显示,一名患者中这些流分类细胞的寡聚性,两名患者中的单克隆性,与处理各自的诊断性淋巴结所确定的TCRγ链基因的模式相同。具有CD3胞质表达的循环CD4表达T淋巴细胞似乎代表具有组织学诊断的AITL的恶性人群。细胞计数法(Comm。Clin。Cytometry)42:180-187,2000.(C)2000 Wiley-Liss,Inc. [参考:28]

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