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通过下一代测序的克隆性评估揭示单个克隆内的多个免疫球蛋白 κ 基因重排。

Multiple Immunoglobulin κ Gene Rearrangements within a Single Clone Unraveled by Next-Generation Sequencing-Based Clonality Assessment.

机构信息

Department of Pathology, Radboud University Medical Centre, Nijmegen, the Netherlands.

Department of Hematology, University Hospital Schleswig-Holstein, Kiel, Germany.

出版信息

J Mol Diagn. 2021 Sep;23(9):1097-1104. doi: 10.1016/j.jmoldx.2021.05.002. Epub 2021 May 19.

Abstract

Clonality assessment of the Ig heavy- and light-chain genes (IGH and IGK) using GeneScan analysis is an important supplemental assay in diagnostic testing for lymphoma. Occasionally cases with an IGK rearrangement pattern that cannot readily be assigned to a monoclonal lymphoma are encountered, whereas the occurrence of biclonal lymphomas is rare, and the result of the IGH locus of these cases is in line with monoclonality. Three such ambiguous cases were assessed for clonality using next-generation sequencing. Information on the sequences of the rearrangements, combined with knowledge of the complex organization of the IGK locus, pointed to two explanations that can attribute seemingly biclonal IGK rearrangements to a single clone. In two cases, this explanation involved inversion rearrangements on the IGK locus, whereas in the third case, the cross-reactivity of primers generated an additional clonal product. In conclusion, next-generation sequencing-based clonality assessment allows for the detection of both inversion rearrangements and the cross-reactivity of primers, and can therefore facilitate the interpretation of cases of lymphoma with complex IGK rearrangement patterns.

摘要

使用 GeneScan 分析评估 IGH 和 IGK 免疫球蛋白重链和轻链基因的克隆性是淋巴瘤诊断检测的重要辅助检测手段。偶尔会遇到 IGK 重排模式难以归为单克隆淋巴瘤的情况,而双克隆淋巴瘤的发生较为罕见,这些病例的 IGH 基因座的结果符合单克隆性。使用下一代测序对这 3 例模棱两可的病例进行了克隆性评估。对重排序列的信息进行分析,并结合对 IGK 基因座复杂结构的了解,有两种解释可以将看似双克隆的 IGK 重排归因于单个克隆。在两种情况下,该解释涉及 IGK 基因座上的倒位重排,而在第三种情况下,引物的交叉反应产生了额外的克隆产物。总之,基于下一代测序的克隆性评估可以检测到倒位重排和引物的交叉反应,因此可以促进对具有复杂 IGK 重排模式的淋巴瘤病例的解释。

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