Transfusion management and hemoglobin‐based oxygen carrier treatment in a patient with anti‐Rh17 antibody

Author:

Mehr Noah1ORCID,Fuja Christine1,Simon Cody1,Carll Timothy1,Alkhateb Rahaf1,Wu Sulin2,Patel Anand A.2ORCID,Aldarweesh Fatima1ORCID

Affiliation:

1. Department of Pathology University of Chicago Chicago Illinois USA

2. Section of Hematology/Oncology, Department of Medicine University of Chicago Chicago Illinois USA

Abstract

AbstractBackgroundA 54‐year‐old Hispanic OPos female with known history of anti‐Rh17 antibodies was diagnosed with Philadelphia‐Chromosome positive (Ph+) acute lymphoblastic leukemia (ALL). Rh17, also known as Hr0, is a high‐frequency antigen composed of several epitopes on the RhCE protein. Anti‐Rh17 antibodies can be made by individuals with missing or varied C/c, E/e antigens. Anti‐Rh17 antibodies are clinically significant given multiple case reports of hemolytic disease of the fetus and newborn (HDFN). Finding compatible units for patients with anti‐Rh17 can be particularly difficult given that only 1 in 100,000 people are Rh17 negative.Study Design and MethodsSearch for compatible units was conducted by the American Rare Donor Program (ARDP) with no leads. After chemotherapy induction and despite erythropoiesis stimulating agent administration, the patient's hemoglobin continued to trend down to a nadir of 2.8 g/dL. Here we report transfusion of incompatible pRBC to this patient with critically symptomatic anemia. HBOC‐201 (Hemopure) was obtained and administered under an emergency compassionate/expanded access designation from the Food and Drug Administration (FDA) under an emergency Investigational New Drug (IND) application.Results and DiscussionOverall difficulties in this case included the challenge of finding compatible units, dilemma of transfusing incompatible units in a patient with severe anemia and obtaining alternatives to blood products. This case report demonstrates the successful use of HBOC‐21 in treating life‐threatening anemia.

Publisher

Wiley

Reference22 articles.

1. Genetic recombination at the human RH locus: a family study of the red‐cell Evans phenotype reveals a transfer of exons 2‐6 from the RHD to the RHCE gene;Huang CH;Am J Hum Genet,1996

2. Rh Blood Group System

3. Hemolytic disease of the fetus and newborn caused by anti-Hr0 in a 27-year-old female with Dc- phenotype: A case report

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