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典型的华氏巨球蛋白血症源自于在体细胞突变停止后但在同种型转换事件之前停滞的B细胞。

Typical Waldenstrom macroglobulinemia is derived from a B-cell arrested after cessation of somatic mutation but prior to isotype switch events.

作者信息

Sahota Surinder S, Forconi Francesco, Ottensmeier Christian H, Provan Drew, Oscier David G, Hamblin Terry J, Stevenson Freda K

机构信息

Molecular Immunology Group, Tenovus Laboratory, Southampton University Hospitals, Southampton, United Kingdom.

出版信息

Blood. 2002 Aug 15;100(4):1505-7.

Abstract

There exists a wide spectrum of IgM-secreting B-cell tumors with different clinical behavior. Knowledge of the V(H) gene status can reveal their origin and clonal history. For Waldenstrom macroglobulinemia (WM), a distinct subtype of lymphoplasmacytic lymphoma, early data on limited sequences showed evidence for somatic mutation. A recent report of one case demonstrated intraclonal mutational activity occurring after transformation, a characteristic of germinal center lymphomas. To extend the investigation, we have analyzed 7 cases of WM. V(H) genes were somatically mutated with no evidence of intraclonal variation in all cases. In contrast to IgM-secreting multiple myeloma, there was no evidence for isotype switch transcripts in any of the cases. These data support the concept that typical WM is derived from a B cell that has undergone somatic mutation prior to transformation, at a point where isotype switch events have not been initiated. (Blood. 2002;100:1505-1507)

摘要

存在一系列具有不同临床行为的分泌IgM的B细胞肿瘤。了解V(H)基因状态能够揭示它们的起源和克隆史。对于华氏巨球蛋白血症(WM),这是一种淋巴浆细胞淋巴瘤的独特亚型,关于有限序列的早期数据显示了体细胞突变的证据。最近一份关于一个病例的报告表明,在转化后出现了克隆内突变活性,这是生发中心淋巴瘤的一个特征。为了扩展研究,我们分析了7例WM。所有病例中V(H)基因均发生体细胞突变,且无克隆内变异的证据。与分泌IgM的多发性骨髓瘤不同,所有病例中均未发现同种型转换转录本的证据。这些数据支持了这样一种概念,即典型的WM源自一个在转化前已经历体细胞突变的B细胞,此时同种型转换事件尚未启动。(《血液》。2002年;100:1505 - 1507)

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