Wagner F F, Gassner C, Muller T H, Schonitzer D, Schunter F, Flegel W A
Abteilung Transfusionsmedizin, Universitat Ulm and DRK-Blutspendezentrale Ulm, Ulm, Germany.
Blood. 1998 Mar 15;91(6):2157-68.
Rhesus D category VI (DVI) is the clinically most important partial D. DVI red blood cells were assumed to possess very low RhD antigen density and to be caused by two RHD-CE-D hybrid alleles. Because there was no population-based work-up, we screened three populations in central Europe for DVI. Twenty-six DVI samples were detected and examined by exon-specific RHD polymerase chain reaction with sequence-specific primers (PCR-SSP). A new genotype, hereby designated D category VI type III, was characterized as a RHD-Ce(3-6)-D hybrid allele by sequencing of the cDNA, parts of intron 1, and by PCR-restriction fragment length polymorphism (PCR-RFLP) of intron 2. Rhesus introns 5 and 6 were sequenced and the 3' breakpoints of all known DVI types shown to be distinct. We differentiated the 5' breakpoints of DVI type I and DVI type II by a newly devised RHD-PCR. Thus, the DVI phenotype originated in at least three independent molecular events. Each DVI type showed distinct immunohematologic features in flow cytometry. The number of RhD proteins accessible on the red blood cells' surface of DVI type III was normal (about 12,000 antigens/cell; DVI type I, 500; DVI type II, 2,400) based on the determination of an RhD epitope density profile. DVI type II and DVI type III occurred as CDe haplotypes, and DVI type I as a cDE haplotype. The distribution of the DVI types varied significantly in three German-speaking populations. Genotyping strategies should take account of allelic variations in partial RhD. The reconsideration of previous serologic and clinical data for partial D in view of the underlying molecular structures may be worthwhile.
恒河猴D类别VI(DVI)是临床上最重要的部分D型。DVI红细胞被认为具有极低的RhD抗原密度,是由两个RHD-CE-D杂交等位基因引起的。由于缺乏基于人群的研究,我们在中欧的三个人群中筛查了DVI。通过外显子特异性RHD聚合酶链反应和序列特异性引物(PCR-SSP)检测并检查了26个DVI样本。通过对cDNA、内含子1的部分区域进行测序以及对内含子2进行PCR-限制性片段长度多态性分析(PCR-RFLP),确定了一种新的基因型,在此命名为D类别VI型III,其特征为RHD-Ce(3-6)-D杂交等位基因。对恒河猴内含子5和6进行了测序,结果显示所有已知DVI类型的3'断点各不相同。我们通过新设计的RHD-PCR区分了DVI I型和DVI II型的5'断点。因此,DVI表型至少起源于三个独立的分子事件。每种DVI类型在流式细胞术中都表现出独特的免疫血液学特征。根据RhD表位密度谱的测定,DVI III型红细胞表面可及的RhD蛋白数量正常(约12,000个抗原/细胞;DVI I型为500个;DVI II型为2,400个)。DVI II型和DVI III型以CDe单倍型出现,DVI I型以cDE单倍型出现。三种讲德语的人群中DVI类型的分布差异显著。基因分型策略应考虑部分RhD中的等位基因变异。鉴于潜在的分子结构,重新审视先前关于部分D的血清学和临床数据可能是值得的。