Transfusion · 2003 · 55 citations · 21 references
Life SciencesImmunologyMolecular BiologyClinical ImmunologyImmunogeneticsMolecular DiagnosticsAutoantigensBlood TypingHuman Leukocyte Antigen SystemMajor Histocompatibility ComplexAberrant Antigen ProcessingAmino AcidsCold Agglutinin EvaluationEpitope GenerationEpitope SelectionGenomic Dna AnalysisHaplotype VariationReactivity
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.
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Molecular Basis of Weak D Phenotypes
Franz F. Wagner, Christoph Gassner, Thomas Müller et al. · Blood · 1999 · 336 citations
Molecular Basis of Weak D Phenotypes
Franz F. Wagner, Christoph Gassner, Thomas Müller et al. · Blood · 1999 · 331 citations
RHD gene deletion occurred in the Rhesus box
Franz F. Wagner, Willy A. Flegel · Blood · 2000 · 319 citations
RHD positive haplotypes in D negative Europeans
Franz F. Wagner, Alexander Frohmajer, Willy A. Flegel · BMC Genetics · 2001 · 310 citations · Full text