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Extended Red Blood Cell Genotyping to Investigate Immunohematology Problems

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초록

Red blood cell (RBC) genotyping is recommended to limit alloimmunization in patients with sickle cell disease or thalassemia [1]. RBC genotyping can resolve the serologic weak D phenotype and inconclusive RhD typing in obstetrics and identify the RBC phenotype in patients with autoantibodies or a positive direct antiglobulin test (DAT) [2]. DNA-based RBC typing has better accuracy and provides more information on RBC antigens than typical phenotyping [1]. We report a challenging case of a pregnant patient in whom a lack of compatible RBCs, based on RBC genotyping, suggested the presence of anti-Dib and anti-E specificities. To our knowledge, extended RBC genotyping was used to obtain compatible RBC units for the first time in Korea.

Abstract

Red blood cell (RBC) genotyping is recommended to limit alloimmunization in patients with sickle cell disease or thalassemia [1]. RBC genotyping can resolve the serologic weak D phenotype and inconclusive RhD typing in obstetrics and identify the RBC phenotype in patients with autoantibodies or a positive direct antiglobulin test (DAT) [2]. DNA-based RBC typing has better accuracy and provides more information on RBC antigens than typical phenotyping [1]. We report a challenging case of a pregnant patient in whom a lack of compatible RBCs, based on RBC genotyping, suggested the presence of anti-Dib and anti-E specificities. To our knowledge, extended RBC genotyping was used to obtain compatible RBC units for the first time in Korea.

참고문헌 (10)

  1. Casas J, "Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease", Transfusion, 55, pp.1388~1393 (2015)[DOI]
  2. Keller MK, "The role of red cell genotyping in transfusion medicine", Immunohaematology, 31, pp.49~52 (2015)
  3. Fung MK, "Technical Manual. 18th ed." (2014), AABB Press
  4. Hong YJ, "Genotyping of 22 blood group antigen polymorphisms and establishing a national recipient registry in the Korean population", Ann Hematol, 95, pp.985~991 (2016)[DOI]
  5. Park MH, "A case of hemolytic disease of the newborn due to anti-Dib Antibody", J Korean Soc Neonatol, 6, pp.268~267 (1999)
  6. 최지원, "A Case of Mild Hemolytic Disease of the Fetus and Newborn - The First Case of Anti-Di b Identified on Prescreening Test during Pregnancy -", 대한수혈학회지, 21(2), pp.165~170 (2010), 대한수혈학회
  7. Kim HC, "A case of hemolytic disease of the newborn due to anti-Dib antibody", Korean J Blood Transfus, 5, pp.151~158 (1994)
  8. Oh EJ, "Severe hemolytic disease of the newborn due to anti-Dib treated with phototherapy and intravenous immunoglobulin", Ann Clin Lab Sci, 38, pp.80~82 (2008)
  9. 이민영, "Di(a+b-) 표현형을 가진 환자에서 발견된 항-Dib 2예: 국내 희귀혈액형 헌혈자 등록 사업의 필요성 제안", Laboratory Medicine Online, 7(2), pp.79~82 (2017), 대한진단검사의학회
  10. Flegel WA, "Integration of red cell genotyping into the blood supply chain: a population-based study", Lancet Haematol, 2, pp.e282~e288 (2015)[DOI]

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