Haematologica (Dec 2007)

Rituximab for prevention of delayed hemolytic transfusion reaction in sickle cell disease

  • F. Noizat-Pirenne,
  • D. Bachir,
  • P. Chadebech,
  • M. Michel,
  • A. Plonquet,
  • J.-C. Lecron,
  • F. Galactéros,
  • P. Bierling

DOI
https://doi.org/10.3324/haematol.12074
Journal volume & issue
Vol. 92, no. 12

Abstract

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Delayed hemolytic transfusion reaction (DHTR), a life-threatening transfusion complication in sickle cell disease (SCD), is characterized by a marked hemoglobin drop with destruction of both transfused and autologous red blood cells (RBCs) and exacerbation of SCD symptoms. One mechanism of RBCs destruction is auto-antibody production secondary to transfusion. As rituximab specifically targets circulating B cells, we thought that it could be beneficial in preventing this immune-mediated transfusion complication. We report the case of a SCD patient who previously experienced DHTR with auto-antibodies and who needed a new transfusion. DHTR recurrence was successfully prevented by rituximab administration prior transfusion, supporting the safe use of rituximab to prevent DHTR in SCD patients as a second line approach when other measures failed.