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首页> 外文期刊>American Journal of Hematology >Clonal immunoglobulin lambda light-chain gene rearrangements detected by next generation sequencing in POEMS syndrome
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Clonal immunoglobulin lambda light-chain gene rearrangements detected by next generation sequencing in POEMS syndrome

机译:诗歌综合征中下一代测序检测的克隆免疫球蛋白λ轻链基因重排

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摘要

Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare plasma cell dyscrasia characterized by polyneuropathy, organomegaly, endocrinopathy, extravascular fluid overload, M protein, and a myriad of skin changes. The pathogenesis is poorly understood, but monoclonal plasma cells are.-restricted and these immunoglobulin. light chain variable (IGLV) region genes are derived from only two germlines, either IGLV1-44 or 1-40. Here we analyzed the clonal IGLV gene rearrangements of genomic DNA samples of bone marrow mononuclear cells using next-generation sequencing (NGS) to understand the clonal composition of IGLV genes in patients with POEMS syndrome (n = 30). The dominant IGLV gene rearrangement of POEMS syndrome-specific germline sequences were significantly increased in 11 POEMS patients (36.7%; IGLV1-44: n = 9, IGLV1-40: n = 2). In some cases, IGLV gene rearrangement clone was not detected as significant increase but was detected using cDNA samples by heteroduplex (HD) analysis and Sanger sequencing, suggesting that the quite small number of monoclonal plasma cells may produce large quantity of mRNA of monoclonal proteins. However, significant increase of dominant clone sizes was not directly linked to the initial disease status. On the other hand, in cases with significantly increased dominant clones, they decreased and increased accompanying with disease remission and relapse. These data demonstrate that monoclonal plasma cells are related to the pathogenesis of POEMS syndrome.
机译:多变疗法,有机疗法,内分泌,M蛋白和皮肤变化(诗歌)综合征是一种稀有的血浆细胞多变,其特征在于多变疗法,有机大乐,内分泌,血管外液过载,M蛋白和无数的皮肤变化。发病机制较差,但单克隆血浆细胞是限制性和这些免疫球蛋白。轻链可变(IGLV)区基因仅衍生自IGLV1-44或1-40。在这里,我们使用下一代测序(NGS)分析了骨髓单核细胞的基因组DNA样品的克隆IgLV基因重排,以了解诗歌综合征患者IGLV基因的克隆组合物(n = 30)。诗歌综合征特异性种系序列的显性IgLV基因重排在11例患者中显着增加(36.7%; IgLv1-44:n = 9,IgLv1-40:n = 2)。在一些情况下,未检测到IgLV基因重排克隆,但使用异拷贝(HD)分析和Sanger测序使用cDNA样品进行显着增加,表明相当多的单克隆血浆细胞可以产生大量的单克隆蛋白mRNA。然而,显着增加的主要克隆尺寸与初始疾病状态没有直接相关。另一方面,在显着增加的显性克隆增加的情况下,它们随着疾病缓解和复发而随之而来。这些数据表明单克隆血浆细胞与诗歌综合征的发病机制有关。

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