Cerebrospinal fluid TNF-α, IL-6, and IL-8 in children with bacterial meningitis
Rajniti Prasad1, Rishi Kapoor1, Ragini Srivastava2
1Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Insights
Elevated cerebrospinal fluid levels of tumor necrosis factor-α, interleukin-6, and interleukin-8 are significantly increased in children with bacterial meningitis. These cytokine measurements show high accuracy for diagnosing bacterial meningitis in children.
Area of Science:
- Pediatric Infectious Diseases
- Neuroinflammation
- Biomarker Discovery
Background:
- Bacterial meningitis is a serious infection in children requiring accurate and timely diagnosis.
- Cerebrospinal fluid (CSF) cytokine profiles are being investigated as potential diagnostic markers.
Purpose of the Study:
- To evaluate CSF concentrations of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-8 (IL-8) in children with bacterial meningitis.
- To assess the diagnostic utility of these cytokines in differentiating bacterial from viral meningitis.
Main Methods:
- CSF samples were collected from children diagnosed with bacterial meningitis (n=57), viral meningitis (n=15), and healthy controls (n=15).
- Levels of TNF-α, IL-6, and IL-8 were quantified using enzyme-linked immunosorbent assay (ELISA).
- Statistical analysis included receiver operating characteristic (ROC) curve analysis to determine sensitivity and specificity.
Main Results:
- CSF levels of TNF-α, IL-6, and IL-8 were significantly elevated in children with bacterial meningitis compared to viral meningitis and controls (P < 0.001).
- At optimal cutoffs, CSF cytokines demonstrated 100% sensitivity and specificity for bacterial meningitis diagnosis.
- TNF-α, IL-6, and IL-8 showed high sensitivity and specificity in differentiating bacterial from viral meningitis (e.g., TNF-α: 94.7% sensitivity, 86.7% specificity).
Conclusions:
- Elevated CSF TNF-α, IL-6, and IL-8 suggest a role in the pathogenesis of pediatric bacterial meningitis.
- These CSF cytokines may serve as valuable biomarkers for diagnosing bacterial meningitis, especially in cases with diagnostic uncertainty.
Objective:
We evaluated the levels of cerebrospinal fluid concentrations of tumor necrosis factor-α, interleukin-6, and interleukin-8 in bacterial meningitis in children.
Methods:
The study included children up to 14 years of age admitted to a pediatric ward with fever, headache, vomiting, and seizures. The diagnosis of bacterial meningitis was based on clinical features: physical examination, blood and cerebrospinal fluid cytochemical findings, Gram stain, and bacterial culture. The cerebrospinal fluid levels of tumor necrosis factor-α, interleukin-6, and interleukin-8 were measured in 57 children with bacterial meningitis, 15 with viral meningitis, and 15 controls by enzyme-linked immunosorbent assay methods.
Results:
The mean concentrations of cerebrospinal fluid, tumor necrosis factor-α, interleukin-6, and interleukin-8 were 1108 ± 183, 652 ± 287, and 442 ± 120 pg/mL, respectively, in children with bacterial meningitis and were significantly increased in those in the viral meningitis group (tumor necrosis factor-α : 711 ± 105, IL-6 : 272 ± 161, IL-8 : 175 ± 62 pg/mL; P < 0.001) or control (390 ± 37, 59 ± 17, 19 ± 13 pg/mL, respectively, P < 0.001). At optimum cutoff level based on the receiver operating characteristic curve, cerebrospinal fluid cytokines (tumor necrosis factor-α, interleukin-6, and interleukin-8) showed sensitivity and specificity of 100% for the diagnosis of bacterial meningitis. For differentiation of bacterial from viral meningitis, cerebrospinal fluid level of tumor necrosis factor-α, IL-6, and IL-8 showed sensitivity and specificity of 94.7% and 86.7%, 80.7% and 53.3%, and 89.5% and 86.7%, respectively.
Conclusion:
The increased concentration of cerebrospinal fluid tumor necrosis factor-α, interleukin-6, and interleukin-8 in children with meningitis suggests a role in the pathogenesis of bacterial meningitis and these levels might prove to be useful in children whose diagnosis is in question.
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