Persistent complement-dependent anti-AnWj in a lymphoproliferative disorder: a case study and review
Categoria dell'articolo: Case Report
Pubblicato online: 11 mar 2020
Pagine: 83 - 88
DOI: https://doi.org/10.21307/immunohematology-2019-179
Parole chiave
© 2011 G. Grigoriadis, et al., published by Sciendo
AnWj is a high-incidence antigen present on the red blood cells (RBCs) of greater than 99 percent of the general population. A 58-year-old man underwent autologous hematopoietic stem cell transplantation (HSCT) for stage IVa mantle cell lymphoma. This procedure was complicated by failure to engraft, necessitating ongoing support with blood components. After a 2-month period of uneventful transfusion support, the patient experienced increasingly severe reactions with fever and evidence of intravascular hemolysis, including hemoglobinuria. Testing revealed a complement-dependent anti-AnWj. Phenotyping confirmed the AnWj– phenotype. Anti-AnWj was persistent despite immunosuppression, including treatment with allogeneic HSCT. Of interest, the pathogenesis of the downregulation of the graft AnWj in this patient is unclear.