Investigating anti-D in an individual with the weak D type 2 genotype

Immunohematology. 2022 Sep 22;38(3):77-81. doi: 10.21307/immunohematology-2022-046. Print 2022 Sep 1.

Abstract

Anti-D in individuals with a weak D phenotype is an unexpected finding that may require additional investigation to determine whether the anti-D is an autoantibody or alloantibody. Further investigation may also include assessment of the patient's RHD genotype and exclusion of anti-G. We present a case of an 84-year-old man with the weak D type 2 genotype who developed an unexpected anti-D along with anti-C. Individuals with the weak D type 2 genotype are thought not to be at risk for developing alloanti-D, although the distinction between alloanti-D and autoanti-D may be difficult to ascertain. Furthermore, investigations may affect transfusion recommendations. This patient was restricted to crossmatch-compatible, D-C- red blood cells even though the clinical significance of the anti-D was uncertain. This report is one of a few reported cases of an individual with the weak D type 2 genotype with demonstrable anti-D but without evidence for alloanti-D.

Keywords: alloanti-D; anti-D; anti-G; autoanti-D; weak D type 2.

Publication types

  • Case Reports

MeSH terms

  • Blood Grouping and Crossmatching*
  • Genotype
  • Humans
  • Isoantibodies
  • Phenotype
  • Rh-Hr Blood-Group System / genetics
  • Rho(D) Immune Globulin* / genetics

Substances

  • Isoantibodies
  • RHO(D) antibody
  • Rh-Hr Blood-Group System
  • Rho(D) Immune Globulin