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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >A minority of concurrent monoclonal lymphocytes and plasmacytic cells sharing light chains are genetically related in putative lymphoplasmacytic lymphoma.
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A minority of concurrent monoclonal lymphocytes and plasmacytic cells sharing light chains are genetically related in putative lymphoplasmacytic lymphoma.

机译:少数共有轻链的同时存在的单克隆淋巴细胞和浆细胞在遗传性浆细胞性淋巴瘤中具有遗传相关性。

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摘要

Flow cytometric cell sorting combined with molecular gene rearrangement analysis was used to detect and to further characterize simultaneously occurring phenotypically distinct B cell monoclonal lymphoid and monoclonal plasma cell populations from 38 individual specimens. By sorting and subsequent gene rearrangement analysis, separate or identical monoclonality genotypes could be revealed and confirmed. In only 13 of 38 specimens, the B lymphoid cells and plasma cell populations showed an identical genotypic profile, while 25 had non-identical profiles (including 4 process control specimens). The majority of the genotypically identical group had a phenotype consistent with Waldenstrom's/lymphoplasmacytic lymphoma (WM/LPL), while WM/LPL phenotype was present in 16/25 of the non-identical cases. Proof of an identical monoclonal genotype for plasmacytic and B-lymphoid cell populations must be used to define WM/LPL as a distinct entity in the clinical setting of monoclonal lymphoid and plasma cells expressing the same light chains. Conversely, the confirmation of genotypically distinct populations can significantly improve confidence in diagnostic and prognostic decisions in specimens with B lymphoid lymphomas and a concurrent, possibly smoldering myeloma or multiple myeloma. These techniques are requisite in future clinical studies for diagnosis and prognosis in these diseases.
机译:流式细胞仪分选结合分子基因重排分析用于检测和进一步表征来自38个标本的同时发生的表型不同的B细胞单克隆淋巴样和单克隆浆细胞群体。通过分类和随后的基因重排分析,可以揭示和确认单独或相同的单克隆基因型。在38个标本中,只有13个的B淋巴样细胞和浆细胞群显示出相同的基因型谱,而25个具有不相同的谱图谱(包括4个过程对照标本)。在基因型相同的组中,大多数具有与Waldenstrom /淋巴浆细胞性淋巴瘤(WM / LPL)一致的表型,而在不相同病例中有16/25出现WM / LPL表型。在浆细胞和表达相同轻链的浆细胞的临床环境中,必须使用针对浆细胞和B淋巴细胞群体的相同单克隆基因型的证据来将WM / LPL定义为不同的实体。相反,在B型淋巴瘤和并发的,可能是闷烧的骨髓瘤或多发性骨髓瘤的标本中,基因型不同的人群的确诊可以显着提高对诊断和预后决策的信心。这些技术对于这些疾病的诊断和预后在未来的临床研究中是必不可少的。

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