Table 1.
Approximate alloimmunization rates to non-ABO blood group antigens reported in various patient populations
Population | Most common antibody specificity | Approximate alloimmunization rate | Exposure | Other notes/comments |
---|---|---|---|---|
General transfused population [6, 7, 8, 9, 10] | K, E | <1–4% | RBC transfusion | primarily retrospective studies; alloimmunization rates of 8–10% reported in prospective transfusion studies |
Rh-negative healthy volunteers [21, 22] | D | 83–93% | intravenous RBC infusion | anti-E, anti-C and/or anti-G also detected in some volunteers |
Young children [23, 24, 25, 26, 27, 28] | K, E | vanishingly rare | RBC transfusion | may be associated with severe infection or treatment with infliximab. |
Hospitalized, non-oncology patients [14, 15] | primarily C, E, K | 20–30% | RBC transfusion | military combat veterans may be at increased risk compared to civilians |
SCD [29, 30, 32, 33] | primarily C, E, K | Up to 47% | RBC transfusion | several guidelines recommend the provision of C, E and K matched RBCs for transfusion in this population |
Myelodysplastic syndromes [40, 41, 42, 43] | Rh and K | Up to 58.6% | RBC transfusion | most studies utilized FAB criteria for diagnosis of MDS |
Thalassemias [34, 35, 36, 37] | Rh and K | Up to 37% | RBC transfusion | |
Pregnancy (prior to RhIg) [86] | D | 7.2% | fetal-maternal hemorrhage | substantially reduced by the introduction of Rh(D) immune globulin |
AIDS [87] | – | none reported | RBC transfusion | further study needed |
AABB = American Association of Blood Banks; FAB = French American British classification of hematologic diseases
MDS = myelodysplastic syndromes; SCD = sickle cell disease.