Genotyping in Transfusion Medicine: A New Era of Precision and Efficiency

In transfusion medicine, precision can make the difference in mitigating unwanted immune reactions. Central to this precision, molecular genotyping is transforming antigen typing by bringing a new level of efficiency to transfusion management.
Why Genotype?
Traditional phenotyping methods serve us well, but they come with limitations. Genotyping offers a comprehensive look into blood antigen makeup of both recipients and donors that can:
- Enable Antigen Typing regardless of recent transfusion or when RBCs are sensitized with antibody
- Identify blood group variants that are clinically relevant for defining the correct antigen type
- Provide extensive antigen profiles including certain rare types to aid in the resolution of complex antibody identifications
- Build robust donor databases with well-characterized antigen profiles
Putting Patients First
Genotyping isn’t another lab test. It is an advancement in blood typing. For individuals with sickle cell disease (SCD) and thalassemia, genotyping allows for extended antigen-matching, a practice that has been shown to reduce alloimmunization rates by up to 30 percent.1,2 Moreover, the American Society of Hematology now recommends Rh and K antigen-matching for transfusion-dependent patients with hemoglobinopathies and patient genotyping is the most efficient way to achieve that goal. This transfusion management change translates into better post-transfusion outcomes with the prospect of a longer life expectancy ³. Furthermore, antigen-matching has been shown to extend transfusion intervals while improving the quality of life for these patients.4
Genotyping also applies to other patient groups who are multi-transfused. Antibody screening and crossmatching is challenging for patients with warm autoimmune hemolytic anemia or are receiving monoclonal antibody therapies that interfere with serologic testing. Proactive genotyping these patients helps the lab know what alloantibodies the patient can make and those they will not.
A Win for Blood Banks
Operationally, genotyping is a game-changer. It’s up to 50% more cost-effective than sourcing antigen-negative units⁵, reduces reagent use⁶, and cuts turnaround time from 3+ hours to under 1 hour7.
It also enables smarter inventory management:
- Preserve D negative units and reduce waste8a,8,9
- Identify patients with genetic mutations (e.g., GATA in Duffy B negative individuals) who can safely receive otherwise incompatible blood10
The Bottom Line
Genotyping is redefining transfusion medicine—making it more precise, personalized, and efficient. As healthcare systems strive for better outcomes and smarter resource use, molecular blood typing stands out as a powerful tool to meet those goals.
1. Leal, I., et al. (2023). Transfusion and Apheresis Science, 62(6), 103813
2. Belsito A, et al. Transfusion and Apheresis Science. 2019 Feb;58(1):65-71
3. Telen et al. Transfusion. 2015 Jun;55(6 Pt 2):1378-87
4. Da Costa DC et al. Rev Bras Hematol Hemoter. 2013;35(1):35-8
5. Shafi et al, Transfusion. 2014 May;54(5):1212-9
6. Winkler et al, Immunohematology. 2012;28(1):24-6
7. Shafi et al, Transfusion. 2014 May;54(5):1212-9
8a Chou et al. Blood Advances 2020 ;4(2): 327-355
8. Sandler et. al Transfusion. 2015 Mar;55(3):680-9
9. Flegel. Transfusion and Apheresis Science, 2011 Feb;44(1):81-91
10. Peiper et al. J Exp Med. 1995 Apr1;181(4):1311-7