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原发性血小板增多症中造血细胞的克隆分析。

Clonal analysis of haemopoietic cells in essential thrombocythaemia.

作者信息

el Kassar N, Hetet G, Li Y, Brière J, Grandchamp B

机构信息

INSERM U409, Faculté de Médecine X, Bichat, Paris, France.

出版信息

Br J Haematol. 1995 May;90(1):131-7. doi: 10.1111/j.1365-2141.1995.tb03391.x.

Abstract

Essential thrombocythaemia (ET) is a myeloproliferative disease (MPD) predominantly involving the platelet lineage, with a diagnosis often difficult to establish in practice. The demonstration of a clonal haemopoiesis can contribute to diagnosis. The clonal origin of blood cells can be assessed in female patients using X-chromosome-linked polymorphisms, assuming a random inactivation of the X chromosome. The human androgen receptor gene HUMARA has been used for this purpose, taking advantage of a highly polymorphic trinucleotide repeat in the first exon. The close proximity of the polymorphic trinucleotide repeat to four methylation sites permits a clonal analysis based on the polymerase chain reaction. We have used this technique to study the clonality of haemopoietic cells in 32 patients with ET and 23 age-matched control heterozygotes for the HUMARA polymorphism. A monoclonal pattern of haemopoiesis was detected in unfractionated nucleated blood cells from 22 patients, suggesting that haemopoiesis is essentially monoclonal in a majority of cases in this disease. In some patients a monoclonality of granulocytes was documented, whereas the mononuclear fraction had a polyclonal pattern of X-inactivation. Finally, in two patients for whom a polyclonality had been found in unfractionated blood, analysis of G6PD transcripts in platelets revealed a clonal megakaryocytopoiesis. These findings confirm the heterogeneity of haematological abnormalities in ET patients and the potential utility of a multifaceted laboratory approach to investigate these patients.

摘要

原发性血小板增多症(ET)是一种主要累及血小板谱系的骨髓增殖性疾病(MPD),在实际中诊断往往难以确立。克隆性造血的证明有助于诊断。假设X染色体随机失活,可利用X染色体连锁多态性评估女性患者血细胞的克隆起源。人类雄激素受体基因HUMARA已用于此目的,利用了第一个外显子中高度多态的三核苷酸重复序列。多态性三核苷酸重复序列与四个甲基化位点紧密相邻,允许基于聚合酶链反应进行克隆分析。我们使用该技术研究了32例ET患者和23例年龄匹配的HUMARA多态性杂合对照者造血细胞的克隆性。在22例患者未分离的有核血细胞中检测到单克隆造血模式,表明在该疾病的大多数病例中造血本质上是单克隆的。在一些患者中记录到粒细胞单克隆性,而单核细胞部分具有多克隆X失活模式。最后,在两名未分离血液中发现多克隆性的患者中,血小板中G6PD转录本的分析显示克隆性巨核细胞生成。这些发现证实了ET患者血液学异常的异质性以及多方面实验室方法研究这些患者的潜在效用。

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