Körmöczi Günther F, Förstemann Elisabeth, Gabriel Christian, Mayr Wolfgang R, Schönitzer Diether, Gassner Christoph
Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, Austria.
Transfusion. 2005 Oct;45(10):1574-80. doi: 10.1111/j.1537-2995.2005.00580.x.
Weak D types are thought to express rather quantitative than qualitative D antigen variants. Distinct type-specific phenotypes and weak D cases with anti-D alloimmunization, however, suggest a variable degree of D antigen alteration.
Variant D types were investigated by use of molecular typing, RHD sequencing, extended serologic D antigen investigations, and flow cytometric D antigen density determination.
Two novel weak D types were discovered, termed weak D type 31 and 32 with single RHD nucleotide substitutions coding for amino acid exchanges in predicted intracellular RhD polypeptide stretches, with antigen densities of approximately 130 and 50 D sites per red blood cell, respectively. Adsorption-elution technique-supported D epitope mapping of these two weak D types, the recently described weak D type 26, and of the most common Central European weak D types (weak D types 1, 2, 3, 4.0, and 4.1) demonstrated the expression of all tested D epitopes. In contrast, a distinct D epitope loss was detected in weak D type 15 and partial D control samples.
All novel and prevalent weak D types expressed all tested D epitopes. Our results indicate that adsorption-elution techniques may be of advantage whenever D epitope loss is suspected in extremely weak D variants.
弱D型被认为表达的是数量而非质量上的D抗原变体。然而,不同的型特异性表型以及伴有抗-D同种免疫的弱D病例表明D抗原改变程度存在差异。
通过分子分型、RHD测序、扩展血清学D抗原检测以及流式细胞术D抗原密度测定对变异D型进行研究。
发现了两种新型弱D型,分别称为弱D型31和32,其RHD单核苷酸替换导致预测的细胞内RhD多肽片段中的氨基酸交换,每个红细胞的抗原密度分别约为130和50个D位点。吸附洗脱技术支持对这两种弱D型、最近描述的弱D型26以及最常见的中欧弱D型(弱D型1、2、3、4.0和4.1)进行D表位图谱分析,结果显示所有测试的D表位均有表达。相比之下,在弱D型15和部分D对照样本中检测到明显的D表位缺失。
所有新型和常见的弱D型均表达所有测试的D表位。我们的结果表明,每当怀疑极弱D变体存在D表位缺失时,吸附洗脱技术可能具有优势。