Open AccessScreening for DEL phenotype in RhD negative Indians
Author(s) -
Kulkarni Swati,
Parchure Disha S.,
Gopalkrishnan Vidya,
Madkaikar Manisha
Publication year - 2018
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.22288
Subject(s) - allele , phenotype , rh blood group system , population , antigen , serology , biology , genetics , microbiology and biotechnology , immunology , medicine , gene , antibody , environmental health
Background DEL phenotype represents a very weak form of D variant detected only by adsorption and elution technique. DEL phenotype individuals mistyped as RhD‐negative can lead to alloimmunization after transfusion or pregnancy. Molecular techniques have now been used to identify DEL variants. They are commonly encountered in the East Asian population with RHD (K409K) being the most frequent allele. RHD (M295I) is the most common DEL allele in Caucasians. As there is a paucity of data on DEL phenotype in the Indian population, the study aims to screen RhD negative individuals for two most common DEL mutations. Material and Methods EDTA blood was collected from 900 RhD negative individuals. Serological analysis included testing for the five major Rh antigens‐ C, c, D, E, and e by tube technique. Samples showing negative reaction for the presence of D antigen by Indirect Antiglobulin test were further tested for DEL phenotype by adsorption and elution technique. Molecular analysis involved DNA extraction and testing by PCR ‐ SSP for RHD (K409K) and RHD (M295I) DEL alleles. Results Rh phenotyping showed 153 Rh negative individuals with r'r, ten with r’’r and 737 with rr phenotype. All the samples tested negative for RhD antigen by adsorption and elution method. The two common DEL mutations RHD (K409K) and RHD (M295I) were also not detected in the study population. Conclusion The study population showed the absence of the two common DEL alleles, concluding the variant to be rare. A comprehensive study with a larger sample size to look for other DEL mutations should be performed.