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用于自然杀伤细胞增殖克隆性诊断的人类雄激素受体X染色体失活检测

The human androgen receptor X-chromosome inactivation assay for clonality diagnostics of natural killer cell proliferations.

作者信息

Boudewijns Michaël, van Dongen Jacques J M, Langerak Anton W

机构信息

Department of Immunology, Erasmus MC, University Medical Center, 3015 GE Rotterdam, The Netherlands.

出版信息

J Mol Diagn. 2007 Jul;9(3):337-44. doi: 10.2353/jmoldx.2007.060155.

Abstract

Clonality is a frequently exploited characteristic of lymphoid malignancies. However, in the natural killer (NK) cell subset of large granular lymphocyte proliferations, clonality is difficult to prove because of the lack of specific genetic markers, such as immunoglobulin or T-cell receptor gene rearrangements. The human androgen receptor (HUMARA) assay, a polymerase chain reaction-based X-chromosome inactivation assay, is a potential diagnostic tool in these disorders. Although there is much experience with X-chromosome inactivation assays in myeloid proliferations, these assays have found only very limited application in clonality assessment of NK cell proliferations. We applied the HUMARA assay in laboratory diagnostics for detection of clonality in NK cell proliferations. We describe its test performance and report three cases in which clonality of NK cell populations was investigated by use of this assay. Our results demonstrate the usefulness of the HUMARA assay in the diagnostic workup of NK cell proliferations.

摘要

克隆性是淋巴系统恶性肿瘤经常呈现的一个特征。然而,在大颗粒淋巴细胞增殖的自然杀伤(NK)细胞亚群中,由于缺乏特异性遗传标记,如免疫球蛋白或T细胞受体基因重排,克隆性很难得到证实。人雄激素受体(HUMARA)检测是一种基于聚合酶链反应的X染色体失活检测方法,是诊断这些疾病的一种潜在工具。虽然在髓系增殖性疾病的X染色体失活检测方面已有很多经验,但这些检测方法在NK细胞增殖的克隆性评估中应用非常有限。我们将HUMARA检测应用于实验室诊断,以检测NK细胞增殖中的克隆性。我们描述了其检测性能,并报告了3例使用该检测方法研究NK细胞群体克隆性的病例。我们的结果证明了HUMARA检测在NK细胞增殖诊断检查中的实用性。

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