Chen Qing, Hustinx Hein, Flegel Willy A
Department of Transfusion Medicine, University Hospital, Ulm, Germany.
Transfusion. 2006 May;46(5):766-72. doi: 10.1111/j.1537-2995.2006.00795.x.
The example of ceRT proved that the expression of some D epitopes does not require D-specific amino acids. This allele denoted as RHce(R154T) caused the "false-positive" reactions that were observed in ccddee blood donors who typed positive for the D antigen with some monoclonal anti-D. No other example exposing a similar molecular mechanism was known.
Eleven donor and 1 patient ccddee samples were collected in Switzerland that typed "false-positive" with some monoclonal anti-D in bromelain technique. Their RHCE alleles were determined by nucleotide sequencing from genomic DNA and by a polymerase chain reaction with sequence-specific priming. The D epitope profile was compared to ceRT. The population frequencies were estimated in Switzerland and Germany by serology or at the molecular level, respectively.
The "false-positive" reactions were caused by the RHCE allele RHce(S122L) occurring in the cde haplotype. Its ceSL phenotype expressed few D epitopes that belonged to the D epitope 6 group. The frequency of ceSL among D- donors was about 1:675 in the region of Bern, Switzerland. No ceSL donors were found elsewhere in Switzerland or in southwestern Germany.
ceSL represented the second molecular mechanism for D antigen expression without any D-specific amino acids. ceSL and ceRT were useful to delineate the molecular mechanisms of D expression by RhCE proteins carrying amino acids not representative for the RhD proteins. The ceSL population frequencies differed significantly among three Swiss and German populations.
ceRT的例子证明,一些D抗原表位的表达并不需要D特异性氨基酸。这种等位基因被命名为RHce(R154T),它在一些ccddee血型的献血者中引发了“假阳性”反应,这些献血者用某些单克隆抗-D试剂检测D抗原呈阳性。此前还没有其他类似分子机制的例子。
在瑞士收集了11份献血者和1份患者的ccddee样本,这些样本在菠萝蛋白酶技术中用某些单克隆抗-D检测呈“假阳性”。通过对基因组DNA进行核苷酸测序以及采用序列特异性引物的聚合酶链反应来确定它们的RHCE等位基因。将D抗原表位谱与ceRT进行比较。分别通过血清学方法或分子水平估计了瑞士和德国的群体频率。
“假阳性”反应是由cde单倍型中出现的RHCE等位基因RHce(S122L)引起的。其ceSL表型表达的D抗原表位很少,且属于D抗原表位6组。在瑞士伯尔尼地区,D抗原阴性献血者中ceSL的频率约为1:675。在瑞士其他地区或德国西南部未发现ceSL献血者。
ceSL代表了D抗原表达的第二种分子机制,且不涉及任何D特异性氨基酸。ceSL和ceRT有助于阐明由携带非RhD蛋白代表性氨基酸的RhCE蛋白所介导的D抗原表达的分子机制。ceSL在瑞士和德国的三个群体中的群体频率存在显著差异。