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一种单管四色流式细胞术检测方法,用于评估慢性淋巴细胞白血病中 ZAP-70 和 CD38 的表达。

A single tube, four-color flow cytometry assay for evaluation of ZAP-70 and CD38 expression in chronic lymphocytic leukemia.

机构信息

Department of Pathology, Box 3712, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Am J Clin Pathol. 2010 May;133(5):708-17. doi: 10.1309/AJCPQS4OXJJSZ5KN.

Abstract

We describe a simple and robust flow cytometry assay for ZAP-70 and CD38 expression. The steps required to validate this assay in a clinical flow cytometry laboratory are described. Two criteria were used to characterize ZAP-70 expression into positive, negative, and indeterminate categories and applied to 111 cases of chronic lymphocytic leukemia (CLL) resulting in 29.7% positive, 56.8% negative, and 13.5% indeterminate cases. A sensitivity-specificity crossover plot between ZAP-70 and CD38 suggested a cutoff of 12.5% for defining CD38 positivity. ZAP-70+ cases were significantly more likely to be at a higher clinical stage and, together with CD38+ cases, were more likely to have unmutated IgV(H). However, for individual patients, the concordance between these markers was not perfect. It may be necessary to evaluate several prognostic markers simultaneously in CLL, and availability of convenient assays for ZAP-70 and CD38 is desirable for optimal clinical decision making.

摘要

我们描述了一种简单而稳健的流式细胞术检测 ZAP-70 和 CD38 表达的方法。本文介绍了在临床流式细胞术实验室中验证该检测方法所需的步骤。我们使用了两个标准将 ZAP-70 表达特征分为阳性、阴性和不确定三类,并将其应用于 111 例慢性淋巴细胞白血病(CLL)患者,其中阳性率为 29.7%,阴性率为 56.8%,不确定率为 13.5%。ZAP-70 和 CD38 之间的敏感性特异性交叉点图提示 CD38 阳性的截断值为 12.5%。ZAP-70+病例更有可能处于较高的临床分期,与 CD38+病例一起,更有可能存在未突变的 IgV(H)。然而,对于个别患者,这些标志物之间的一致性并不完美。在 CLL 中可能需要同时评估多个预后标志物,并且需要方便的 ZAP-70 和 CD38 检测方法,以做出最佳的临床决策。

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