Management of a patient with sickle cell disease and multiple red blood cell alloantibodies in preparation for a hematopoietic stem cell transplantation

Author:

Cigna Maude1,Leiva‐Torres Gabriel André2ORCID,Baillargeon Nadia2ORCID,Yanez Jessica Constanzo2,Robitaille Nancy12

Affiliation:

1. Division of Hematology‐Oncology, Department of Pediatrics CHU Sainte‐Justine Montreal Canada

2. Transfusion Medicine Hema‐Quebec Montreal Canada

Abstract

AbstractBackgroundHematopoietic stem cell transplant (HSCT) is currently the only widely available curative option for patients with sickle cell disease (SCD). Alloimmunization in this population is frequent and can complicate transfusion management during the HSCT period. The case of a pediatric patient with severe SCD clinical phenotype, multiple alloantibodies (9), and hyperhemolysis syndrome who underwent haploidentical HSCT is described.Study Design and MethodsThe patient was known for an anti‐e, despite RHCE*01.01 allele, which predicts a C‐ c+ E‐ weak e+ phenotype. Donors matching the patient's extended phenotype were targeted for RHCE genotyping.ResultsDonors homozygotes or heterozygotes for RHCE*01.01 were selected for compatibility analyses and ranked based on strength of reactions. Discordance between zygosity and strength of reactions was observed, as the most compatible donors were heterozygotes for RHCE*01.01. In total, the patient received seven RBC units from two different donors during HSCT process without transfusion reaction or development of new alloantibodies. Six months post‐HSCT, his hemoglobin level is stable at around 120 g/L and his chimerism is 100%.DiscussionThis case highlights the complexity of transfusion management during HSCT of alloimmunized patients with SCD. Collecting sufficient compatible units requires early involvement of transfusion medicine teams and close communication with the local blood provider. Genotyping of donors self‐identifying as Black is useful for identifying compatible blood for those patients but has some limitations. HSCT for heavily alloimmunized patients is feasible and safe with early involvement of transfusion medicine specialists. Further research on the clinical impact of genotypic matching is needed.

Publisher

Wiley

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