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Primary anti-D immunization by DEL red blood cells
Kyeong-Hee Kim1, Kyung-Eun Kim, Kwang-Sook Woo
1Department of Laboratory Medicine, Dong-A University College of Medicine, Busan, Korea. progreen@dau.ac.kr
The Korean Journal of Laboratory Medicine
|September 4, 2009
Summary
Extremely weak D variants (DEL) can cause alloanti-D immunization in recipients, even when donors appear D-negative. This case highlights the need for molecular screening of DEL red blood cells in transfusion medicine.
Area of Science:
- Transfusion Medicine
- Immunology
- Genetics
Background:
- The DEL phenotype, characterized by extremely weak D variants of the RHD gene, is typically detected using adsorption-elution techniques.
- The RHD (K409K, 1227G>A) allelic variant is prevalent in East Asian DEL individuals.
- Previously, no DEL phenotype had been documented to induce primary alloanti-D immunization in East Asia.
Observation:
- A 68-year-old D-negative Korean man developed alloanti-D antibodies after receiving red blood cell (RBC) transfusions from four apparently D-negative donors.
- Routine serological testing identified the donors as D-negative.
- Molecular analysis revealed one donor carried the RHD (K409K) variant.
Findings:
- This case represents the first documented instance of DEL red blood cells with the RHD (K409K) variant inducing primary alloanti-D immunization in an Asian population.
- The DEL phenotype, previously considered non-immunogenic in this population, demonstrated immunogenic potential.
Implications:
- The findings necessitate a re-evaluation of transfusion protocols, particularly concerning RhD-negative donor screening in populations with a high prevalence of DEL variants.
- Molecular methods for detecting RHD gene carriers, such as the RHD (K409K) variant, should be considered for efficient screening.
- This underscores the importance of advanced genotyping for ensuring transfusion safety and preventing alloimmunization, especially in diverse ethnic groups.
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