What is it about?
The transfusion of plasma containing anti-A and anti-B to the Group A or B transfusion recipient can be associated with an unexplained clinically significant hemolytic event. Using an in vitro model, we show that complement-mediated hemolysis can go undetected because the population of red cells with the defect can be completely hemolysed, giving a false negative test for hemolysis.
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Why is it important?
There are disease states where defects in the regulators of complement are acquired. The acquired defect in the regulators of complement, DAF and MIRL, is termed paroxysmal hemoglobinuria, which can be found in patients with myelodysplastic syndrome and aplastic anemia.
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This page is a summary of: Potential impact of complement regulator deficiencies on hemolytic reactions due to minor ABO-mismatched transfusions, Blood Advances, October 2017, American Society of Hematology,
DOI: 10.1182/bloodadvances.2017008805.
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