基因分型
桑格测序
DNA测序
基因型
等位基因
Rh血型系统
分子生物学
生物
遗传学
血型
DNA
计算生物学
抗体
基因
ABO血型系统
作者
Emília Sippert,Evgeniya Volkova,Meagan D. Rippee‐Brooks,Gregory A. Denomme,Willy A. Flegel,Christine Lee,Richardae Araojo,Orieji Illoh,Zhugong Liu,María Rios,Carine Prisco Arnoni,Flávia Roche Moreira Latini,Flavia Sant'Anna Silva,Tatiane Aparecida de Paula Vendrame,Catherine A. Hyland,Glenda Millard,Yew‐Wah Liew,Gayle Teramura,Samantha Harris,Shelley Nakaya Fletcher
标识
DOI:10.1016/j.jmoldx.2024.02.005
摘要
Abstract
Patients who carry RH blood group variants may develop Rh alloantibodies requiring matched red cell transfusions. Serologic reagents for Rh variants often fail to specifically identify variant Rh antigens and are in limited supply. Therefore, red cell genotyping assays are essential for managing transfusions in patients with clinically relevant Rh variants. Well-characterized DNA reference reagents are needed to ensure quality and accuracy of the molecular tests. Eight lyophilized DNA reference reagents, representing 21 polymorphisms in RHD and RHCE, were produced from an existing repository of immortalized B-lymphoblastoid cell lines at CBER/U.S. FDA. The material was validated through an international collaborative study involving 17 laboratories that evaluated each DNA candidate using molecular assays to characterize RHD and RHCE alleles including commercial platforms and laboratory developed testing such as Sanger sequencing, next generation sequencing, and third generation sequencing. The genotyping results showed 99.4% agreement with the expected results for the target RH polymorphisms and 87.9% for RH allele agreement. Most of the discordant RH alleles results were explained by a limited polymorphism coverage in some genotyping methods. Results of stability and accelerated degradation studies support the suitability of these reagents for use as reference standards. The collaborative study results demonstrate the qualification of these eight DNA reagents for use as reference standards for RH blood group genotyping assay development and analytical validation.
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