Further analysis of Del (D‐elute) using polymerase chain reaction (PCR) with RHD gene‐specific primers

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Abstract
Del (D‐elute) in the Rh blood group system is a variant with very weak D antigen and no agglutination is found by the indirect antiglobulin test. This variant is characterized by the presence of anti‐D eluate obtained after an adsorption‐elution test using anti‐D antibodies. We studied here the molecular genetic status of Del by using polymerase chain reaction with sequence‐specific primers (PCR‐SSP). We screened 306 serologically apparent D‐negative Japanese donors comprising 102 Del types for exons 7, 4 and 10 of the RHD gene. No PCR product was found in all 204 non‐Del samples from the D‐seronegative donors. However, PCR products were found in all 102 Del samples and all 70 D‐seropositive samples tested by the three PCR methods for exons 7, 4 and 10 analysis. Del was found with CCee, CcEe and Ccee, but not with CCEe, CcEE, ccEE, ccEe or ccee phenotype. The incidences of Del in the samples with the serological phenotypes CCee, CcEe and Ccee were 80.0% (4/5), 68.2% (45/66) and 61.6% (53/86), respectively. The results provide evidence that Del samples have exons 4, 7 and 10 of an RHD gene present in some form. This is consistent with the evidence that D antigen is present on the cells although only detected by antibody adsorption and elution. The PCR‐SSP method in the present study is useful to confirm Del among serologically apparent D‐negative samples.

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