Abstract
Red blood cell (RBC) blood group alloimmunization remains a major problem in transfusion medicine. This is particularly true for chronically transfused patients. Patients with sickle cell disease (SCD) notoriously make more alloantibodies to RBC antigens than any other patient population, especially alloantibodies to Rh antigens. The classical method of testing for blood group antigens and antibodies is hemagglutination. However, this method has certain limitations, some of which can be overcome by testing DNA to predict a blood type. DNA testing allows conservation of antibodies for confirmation by hemagglutination of predicted antigen negativity. High-throughput DNA array platforms allow for the testing of a relatively large number of donors, thereby providing antigen-negative blood to patients in a novel way and possibly preventing immunization. We performed a study to compare the results obtained by using RH BeadChips™ to laboratory-developed tests and to hemagglutination. Two sets of samples were tested: one set chosen had variant Rh types to challenge the BeadChip™ technology. The other set consisted of random samples from African-American donors and SCD patients to estimate the prevalence of RH alleles. The purpose of this testing was to assess the accuracy and efficiency of the BioArray Solutions prototype BeadChip™ system for RH allele determination.
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Reid, M.E., Hipsky, C.H. (2011). Looking Beyond HEA: Matching SCD Patients for RH Variants. In: Ness, P., Sloan, S., Moulds, J. (eds) BeadChip Molecular Immunohematology. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-7512-6_10
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DOI: https://doi.org/10.1007/978-1-4419-7512-6_10
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