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Anti‐D alloimmunisation in pregnant women with DEL phenotype in China
Author(s) -
Wang M.,
Wang B. L.,
Xu W.,
Fan D. D.,
Peng M. L.,
Pan J.,
Yao P.,
Jiang G. M.,
Wan X. J.
Publication year - 2015
Publication title -
transfusion medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.471
H-Index - 59
eISSN - 1365-3148
pISSN - 0958-7578
DOI - 10.1111/tme.12211
Subject(s) - genotyping , medicine , phenotype , allele , immunogenicity , antigen , immunology , pregnancy , antibody , haemolytic disease , fetus , epitope , gene , biology , genotype , genetics
SUMMARY Objectives To analyse anti‐D alloimmunisation in pregnant women with D‐elute ( DEL ) phenotype in China, for developing a predictive model to evaluate whether a person with the DEL phenotype can receive RhD ‐positive blood. Background Alloanti‐D acquired by pregnancy or transfusion is one of the major causes of both haemolytic disease among newborns and haemolytic transfusion reactions. To date, there is little data available about the antigenic properties and immunogenicity of extremely weak D variants known as DEL . Methods RHD genotyping and D epitope mapping were performed using gene sequencing and comprehensive immunohaematological methods, respectively. DEL pregnant women carrying an RhD ‐positive fetus were tested for the presence of alloanti‐D. Results A total of 130 of 142 (91·5%) pregnant women with a DEL phenotype were confirmed to carry the RHD ( K409K ) allele. Among 12 DEL women who appeared to have RHD‐CE ‐D hybrid alleles, there were 1 RHD‐CE (4–7)‐D , 7 RHD‐CE (4–9)‐D , and 4 RHD‐CE (2–5)‐D alleles. Alloanti‐D antibodies were detected in 6 of 142 DEL women, and all the six women had the partial DEL phenotype. Conclusion The data indicate that partial DEL women appear at risk of alloimmunization to the D antigen. RhD immune globulin prophylaxis is necessary for partial DEL women. Partial DEL patients should receive only RhD ‐negative RBCs , whereas DEL patients with complete expression of antigen can safely receive RhD ‐positive RBCs .