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Updated: May 9, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Elevated serum ApoE levels are associated with bacterial infections in pediatric patients
Pan Fu1, Ai-Min Wang1, Lei-Yan He1
1Clinical Microbiology Laboratory, Department of Nosocomial Infection Control, Children's Hospital of Fudan University, Shanghai 201102, China.
Insights
Serum apolipoprotein E (ApoE) is elevated in children with bacterial infections like sepsis. Reduced expression of ApoE receptors in mice suggests impaired clearance contributes to higher blood levels, potentially aiding bacterial infection diagnosis.
Area of Science:
- Pediatric Infectious Diseases
- Biochemistry
- Immunology
Background:
- Apolipoprotein E (ApoE) plays a role in lipid metabolism and immune response.
- Variations in ApoE levels can indicate underlying health conditions.
Purpose of the Study:
- To determine serum ApoE level variations in pediatric patients with diverse infections.
- To investigate the mechanism behind elevated ApoE during infection.
Main Methods:
- Serum ApoE levels measured via immunoturbidimetric assay in 279 pediatric patients and 58 controls.
- Mouse sepsis model used to assess ApoE and receptor expression via RT-PCR and Western blotting.
Main Results:
- Markedly increased serum ApoE observed in bacterial infections (sepsis, meningitis, pneumonia).
- No significant elevation in aseptic meningitis or Mycoplasma pneumonia.
- Mouse models showed increased serum ApoE and reduced hepatic expression of ApoE and its receptors (LDLR, LRP, SDC1) during sepsis.
Conclusions:
- Serum ApoE may serve as a novel diagnostic indicator for pediatric bacterial infections, particularly sepsis.
- Decreased expression of LDLR, LRP, and SDC1 may impair ApoE clearance, leading to blood accumulation.
Background/Purpose(S):
We aimed to determine the variations in serum apolipoprotein E (ApoE) levels in pediatric patients with a variety of infectious diseases, and to investigate the potential mechanism of elevated ApoE serum levels during infection.
Methods:
A total of 279 pediatric patients with a variety of infections and 58 normal controls were enrolled in this study. Serum ApoE levels were detected using an immunoturbidimetric assay. A mouse sepsis model was established to evaluate the expression of ApoE and its receptors by real-time polymerase chain reaction (RT-PCR) and Western blotting.
Results:
Serum ApoE was markedly increased in cases with bacterial infections including sepsis, bacterial meningitis, and bacterial pneumonia, compared to healthy controls. No significantly elevated serum ApoE levels were observed in aseptic meningitis patients or mycoplasma pneumonia patients. The mice sepsis models showed a similar pattern of increased serum ApoE levels in the early stage of infections. We found reduced expression of ApoE and its receptors in the liver tissues in these mice models.
Conclusion:
Serum ApoE may represent a novel indicator for diagnosis of bacterial infections, especially sepsis, in pediatric patients. The decreased expression of low-density lipoprotein receptor (LDLR), LDL receptor-related protein (LRP), and heparin sulfate proteoglycan (HSPG) syndecan-1 (SDC1) may contribute to reduced ApoE clearance and accumulation in the blood.
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