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目测法与流式细胞术定量检测恶性 T 细胞中异常 CD2 表达。

Visual inspection versus quantitative flow cytometry to detect aberrant CD2 expression in malignant T cells.

机构信息

Flow Cytometry Unit, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cytometry B Clin Cytom. 2010 May;78(3):169-75. doi: 10.1002/cyto.b.20507.


DOI:10.1002/cyto.b.20507
PMID:20020522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2916169/
Abstract

BACKGROUND: Abnormal levels of T-cell antigen expression occur in T-cell neoplasia. We examined CD2 expression in malignant and normal T cells to determine if the level of CD2 expression differed significantly and if quantitation assisted in detecting this difference. METHOD: Flow cytometric immunophenotypic (FCI) evaluation was performed on specimens from 36 patients with mature T-cell neoplasia. Abnormal T cells were identified based upon the abnormal FCI and morphology. Levels of CD2 expression were quantitated using 1:1 PE conjugates of anti-CD2 and QuantiBRITE bead standards to calculate the antibodies bound per cell (ABC). The efficacy of ABC measurement versus simple examination of dots plots was compared. RESULTS: Abnormal levels of CD2 expression were frequently observed in mature T-cell malignancies. The CD2 ABC values were highly sensitive in detecting differences between malignant and normal T cells (P = 0.0028). In most cases (24/32 specimens, 75%), CD2 ABCs differed by >20%. CD2 ABCs had high variability in normal T cells. CONCLUSIONS: CD2 expression by malignant T cells differed significantly from that of normal T-cells by CD2 ABC quantitation. The high variability in normal T-cell CD2 ABCs limited the determination of normal reference ranges and, thus, its utility in the diagnosis of T-cell neoplasia. However, examination of CD2 can help in detection of tumor cells when residual normal T cells are present for comparison. Moreover, the increased sensitivity of CD2 quantitation is valuable in confirming FCI cases where abnormalities in CD2 expression are difficult to appreciate by visual inspection alone.

摘要

背景:T 细胞肿瘤中会出现 T 细胞抗原表达水平异常的情况。我们研究了恶性和正常 T 细胞中 CD2 的表达情况,以确定 CD2 的表达水平是否存在显著差异,以及定量分析是否有助于检测到这种差异。

方法:对 36 例成熟 T 细胞肿瘤患者的标本进行流式细胞术免疫表型(FCI)评估。根据异常的 FCI 和形态学识别异常 T 细胞。使用抗 CD2 的 1:1 PE 缀合物和 QuantiBRITE 珠标准品来定量 CD2 的表达水平,计算每个细胞结合的抗体(ABC)。比较了 ABC 测量与简单的点图检查的效果。

结果:在成熟 T 细胞恶性肿瘤中经常观察到异常的 CD2 表达水平。CD2 ABC 值在检测恶性和正常 T 细胞之间的差异方面具有很高的敏感性(P = 0.0028)。在大多数情况下(24/32 标本,75%),CD2 ABC 差异>20%。正常 T 细胞中 CD2 ABC 的变异性很大。

结论:通过 CD2 ABC 定量,恶性 T 细胞的 CD2 表达与正常 T 细胞明显不同。正常 T 细胞 CD2 ABC 的高变异性限制了正常参考范围的确定,因此限制了其在 T 细胞肿瘤诊断中的应用。然而,当存在残留的正常 T 细胞用于比较时,CD2 的检查有助于检测肿瘤细胞。此外,CD2 定量的敏感性增加在确认仅通过视觉检查难以察觉 CD2 表达异常的 FCI 病例方面具有价值。

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本文引用的文献

[1]
Performance of calibration standards for antigen quantitation with flow cytometry in chronic lymphocytic leukemia.

Cytometry B Clin Cytom. 2007-11

[2]
Quantitative analysis of the expression of glycosylphosphatidylinositol-anchored proteins during the maturation of different hematopoietic cell compartments of normal bone marrow.

Cytometry B Clin Cytom. 2007-1-15

[3]
A comparison of morphologic features, flow cytometry, TCR-Vbeta analysis, and TCR-PCR in qualitative and quantitative assessment of peripheral blood involvement by Sézary syndrome.

Am J Clin Pathol. 2006-3

[4]
T-cell large granular lymphocyte leukemias have multiple phenotypic abnormalities involving pan-T-cell antigens and receptors for MHC molecules.

Am J Clin Pathol. 2005-12

[5]
CD10 and BCL6 expression in the diagnosis of angioimmunoblastic T-cell lymphoma: utility of detecting CD10+ T cells by flow cytometry.

Hum Pathol. 2005-7

[6]
Flow cytometric immunophenotyping of adult T-cell leukemia/lymphoma using CD3 gating.

Am J Clin Pathol. 2005-8

[7]
Monitoring the decrease of circulating malignant T cells in cutaneous T-cell lymphoma during photopheresis and interferon therapy.

Arch Dermatol. 2003-7

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Immunophenotype and TCR-Vbeta repertoire of peripheral blood T-cells in acute infectious mononucleosis.

Blood Cells Mol Dis. 2003

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Demonstration of aberrant T-cell and natural killer-cell antigen expression in all cases of granular lymphocytic leukaemia.

Br J Haematol. 2003-3

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Br J Haematol. 2003-3

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