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Updated: Mar 26, 2026

Measuring Erythrocyte Complement Receptor 1 Using Flow Cytometry
Published on: May 19, 2020
Red blood cell complement receptor one level varies with Knops blood group, α(+)thalassaemia and age among Kenyan
D H Opi1,2, S Uyoga1, E N Orori1
1Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
Insights
Complement receptor one (CR1) on red blood cells (RBCs) influences malaria risk. In Kenyan children, specific CR1 alleles and sickle cell disease (HbSS) increase RBC CR1 levels, while alpha-thalassemia decreases them.
Area of Science:
- Immunogenetics
- Malariology
- Hematology
Background:
- Complement receptor one (CR1) on red blood cells (RBCs) plays a role in Plasmodium falciparum infection and severe malaria risk.
- RBC surface CR1 levels vary significantly among individuals, but the factors influencing this variation, especially in African populations, are not well understood.
- Understanding RBC CR1 level determinants is crucial for interpreting studies on malaria susceptibility.
Purpose of the Study:
- To investigate the factors influencing red blood cell complement receptor one (RBC CR1) level variation in a malaria-endemic region of coastal Kenya.
- To identify genetic and demographic factors associated with RBC CR1 levels in children.
Main Methods:
- Study involved 3535 child residents in a malaria-endemic area of coastal Kenya.
- Analysis of associations between RBC CR1 levels and various factors including Knops blood group alleles, hemoglobin variants (HbSS, sickle cell trait), ABO blood group, alpha-thalassemia, and age.
Main Results:
- CR1 Knops blood group alleles Sl2 and McC(b), and homozygous HbSS were positively associated with higher RBC CR1 levels.
- Sickle cell trait and ABO blood group did not significantly influence RBC CR1 levels.
- Alpha-thalassemia was associated with reduced RBC CR1 levels, potentially due to smaller RBC volume. Age-related changes in RBC CR1 expression were observed throughout childhood.
Conclusions:
- RBC CR1 level in malaria-endemic African populations is a complex trait influenced by multiple genetic and demographic factors.
- Factors such as specific CR1 alleles, sickle cell disease, alpha-thalassemia, and age significantly impact RBC CR1 levels.
- These findings must be considered in future research on CR1 and malaria susceptibility in these populations.
Abstract:
Both the invasion of red blood cells (RBCs) by Plasmodium falciparum parasites and the sequestration of parasite-infected RBCs in the microvasculature are mediated in part by complement receptor one (CR1). RBC surface CR1 level can vary between individuals by more than 20-fold and may be associated with the risk of severe malaria. The factors that influence RBC CR1 level variation are poorly understood, particularly in African populations. We studied 3535 child residents of a malaria-endemic region of coastal Kenya and report, for the first time, that the CR1 Knops blood group alleles Sl2 and McC(b), and homozygous HbSS are positively associated with RBC CR1 level. Sickle cell trait and ABO blood group did not influence RBC CR1 level. We also confirm the previous observation that α(+)thalassaemia is associated with reduced RBC CR1 level, possibly due to small RBC volume, and that age-related changes in RBC CR1 expression occur throughout childhood. RBC CR1 level in malaria-endemic African populations is a complex phenotype influenced by multiple factors that should be taken into account in the design and interpretation of future studies on CR1 and malaria susceptibility.
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