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RHCE等位基因ceRT:D抗原表位6的表达不需要D特异性氨基酸。

The RHCE allele ceRT: D epitope 6 expression does not require D-specific amino acids.

作者信息

Wagner Franz F, Ladewig Birgit, Flegel Willy A

机构信息

Department of Transfusion Medicine, University of Ulm, Ulm, Germany.

出版信息

Transfusion. 2003 Sep;43(9):1248-54. doi: 10.1046/j.1537-2995.2003.00495.x.

Abstract

BACKGROUND

False-positive D typing in patients may lead to anti-D immunization caused by D+ transfusions or by omission of anti-D prophylaxis. Known causes of such errors are RhCE variants carrying RhD-specific amino acids and cold agglutinin activity of some frequently used monoclonal anti-D.

STUDY DESIGN AND METHODS

The molecular basis of eight samples referred because of "false-positive" reactions with some commercial monoclonal anti-D was investigated by PCR and nucleotide sequencing from genomic DNA. PCR with sequence-specific priming was developed to specifically detect the underlying aberrant RHCE allele. The D epitope profile of the allele was determined by serology.

RESULTS

The aberrant reactivity of the samples was caused by the RHCE allele RHCE(R154T) that occurred in a cde haplotype. The phenotype dubbed ceRT expressed the important D epitope 6, which is the target epitope of most monoclonal anti-D used in routine typing.

DISCUSSION

The characterization of ceRT demonstrated a previously unknown mechanism of antigen D expression that does not require any D-specific amino acid. At least for some D epitopes, D-like structures may be mimicked by RhCE proteins carrying amino acid substitutions not representative for RhD.

摘要

背景

患者中D型误判可能会因输注D阳性血液或未进行抗D预防而导致抗D免疫。此类错误的已知原因包括携带RhD特异性氨基酸的RhCE变体以及某些常用单克隆抗D的冷凝集素活性。

研究设计与方法

通过对基因组DNA进行PCR和核苷酸测序,研究了8个因与某些商业单克隆抗D出现“假阳性”反应而送检样本的分子基础。开发了序列特异性引物PCR以特异性检测潜在的异常RHCE等位基因。通过血清学确定该等位基因的D表位谱。

结果

样本的异常反应性是由出现在cde单倍型中的RHCE等位基因RHCE(R154T)引起的。名为ceRT的表型表达了重要的D表位6,这是常规分型中使用的大多数单克隆抗D的靶表位。

讨论

ceRT的特征揭示了一种以前未知的抗原D表达机制,该机制不需要任何D特异性氨基酸。至少对于某些D表位,携带不代表RhD的氨基酸取代的RhCE蛋白可能会模拟D样结构。

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