National Institute for Biological Standards and Control (NIBSC), Potters Bar, Herts, UK.
Vox Sang. 2013 Feb;104(2):144-52. doi: 10.1111/j.1423-0410.2012.01641.x. Epub 2012 Aug 9.
The aim of the study was to evaluate, in an international collaboration, four lyophilised genomic DNA preparations, selected from genotyped and phenotyped donors by the study organisers, for their suitability to standardise and control blood group genotyping procedures for common ancestral Caucasian and Black African alleles.
Twenty-nine laboratories performed 'blind' testing of replicated ampoules of the candidate reference reagents, RBC1 (10/232), RBC4 (10/236), RBC5 (10/238) and RBC12 (10/234), using a range of genotyping procedures, most commonly classical PCR using allele or sequence specific primers.
The majority of laboratories reported blood group genotypes in accordance with those determined by the study organisers and the serological phenotypes. Despite an overall high level of accuracy in genotyping, the identified errors and inconsistencies, and the limited genotyping capabilities of many laboratories, confirmed the need for validated reference materials to control test procedures.
The establishment of RBC1, RBC4, RBC5 and RBC12 as World Health Organization Reference Reagents will facilitate international standardisation of blood group genotyping and ensure that such tests are sufficiently sensitive and specific.
本研究的目的是在国际合作中评估四种冻干基因组 DNA 制剂,这些制剂由研究组织者从经过基因分型和表型分析的供体中选择,以评估其是否适合标准化和控制常见祖先白人和黑人等位基因的血型基因分型程序。
29 个实验室使用一系列基因分型程序(最常见的是使用等位基因或序列特异性引物的经典 PCR)对候选参考试剂 RBC1(10/232)、RBC4(10/236)、RBC5(10/238)和 RBC12(10/234)的重复小瓶进行“盲测”。
大多数实验室报告的血型基因型与研究组织者和血清表型确定的一致。尽管基因分型总体上具有很高的准确性,但所确定的错误和不一致以及许多实验室有限的基因分型能力,证实了需要经过验证的参考材料来控制测试程序。
将 RBC1、RBC4、RBC5 和 RBC12 确立为世界卫生组织参考试剂将促进血型基因分型的国际标准化,并确保此类测试具有足够的灵敏度和特异性。