Ontology highlight
ABSTRACT: Background
Red cell alloimmunization remains a challenge for individuals with sickle cell disease (SCD) and contributes to increased risk of hemolytic transfusion reactions and associated comorbidities. Despite prophylactic serological matching for ABO, Rh, and K, red cell alloimmunization persists, in part, due to a high frequency of variant RH alleles in patients with SCD and Black blood donors.Study design and methods
We compared RH genotypes and rates of alloimmunization in 342 pediatric and young adult patients with SCD on chronic transfusion therapy exposed to >90,000 red cell units at five sites across the USA. Genotyping was performed with RHD and RHCE BeadChip arrays and targeted assays.Results
Prevalence of overall and Rh-specific alloimmunization varied a
SUBMITTER: Israelyan N
PROVIDER: S-EPMC10947898 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature