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[使用标准化BIOMED-2聚合酶链反应方案对原发性皮肤淋巴瘤进行基因分型分析]

[Genotypic analysis in primary cutaneous lymphomas using the standardized BIOMED-2 polymerase chain reaction protocols].

作者信息

Gallardo F, Bellosillo B, Serrano S, Pujol R M

机构信息

Servicio de Dermatología, Hospital del Mar, IMAS, Barcelona, España.

出版信息

Actas Dermosifiliogr. 2008 Oct;99(8):608-20.

Abstract

The European Biomedicine and Health (BIOMED-2) Concerted Action Project BMH4-CT98-3936 has defined standardized protocols for polymerase chain reaction (PCR) amplification of different loci of the T-cell receptor (TCR) and immunoglobulin (Ig) genes with a view to achieving greater sensitivity and specificity in the assessment of clonality of lymphoid neoplasms. To assess T-cell clonality, analysis of TCRbeta gene and TCRdelta rearrangements (useful in cases of Tgammadelta + cell neoplasms) is proposed alongside that of TCRgamma. For analysis of B-cell clonality, along with the framework (FR) III segment of the IgH gene, other segments are studied (FRI, FRII) in addition to Igl and Igk genes or incomplete DJ rearrangements of the IgH gene and the k deleting element. The results of the amplification are read using automatic reading systems (GeneScan) or using a heteroduplex system.

摘要

欧洲生物医学与健康(BIOMED-2)联合行动项目BMH4-CT98-3936已制定了标准化方案,用于对T细胞受体(TCR)和免疫球蛋白(Ig)基因的不同位点进行聚合酶链反应(PCR)扩增,以期在评估淋巴肿瘤的克隆性时获得更高的灵敏度和特异性。为评估T细胞克隆性,除了对TCRγ进行分析外,还建议对TCRβ基因和TCRδ重排进行分析(这对Tγδ+细胞肿瘤病例有用)。对于B细胞克隆性分析,除了IgH基因的框架(FR)III区段外,还研究其他区段(FRI、FRII),以及Igl和Igk基因,或IgH基因的不完全DJ重排和k缺失元件。扩增结果使用自动读取系统(GeneScan)或异源双链系统进行读取。

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