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Updated: Jun 13, 2026

Collecting And Measuring Wound Exudate Biochemical Mediators In Surgical Wounds
Published on: October 20, 2012
Comparative study of cytokine content in the plasma and wound exudate from children with severe burns
E V Mikhal'chik1, J A Piterskaya, L Y Budkevich
1Russian State Medical University, Moscow, Russia. lemik2007@yandex.ru
Insights
Severe burns elevate specific inflammatory cytokines in children. Complicated burns show significantly higher cytokine levels than uncomplicated burns, indicating a heightened systemic inflammatory response.
Area of Science:
- Immunology
- Pediatric Medicine
- Burn Injury Research
Background:
- Severe burns trigger complex inflammatory responses in children.
- Cytokine profiles are crucial indicators of burn severity and complications.
- Understanding local and systemic inflammation is key to managing burn patients.
Purpose of the Study:
- To compare cytokine concentrations in children with severe uncomplicated versus complicated burns.
- To investigate the role of cytokines in the systemic and local inflammatory response post-burn.
- To explore the relationship between plasma and wound exudate cytokine levels and myeloperoxidase activity.
Main Methods:
- Measurement of 27 cytokines in blood plasma from pediatric burn patients.
- Comparison of cytokine levels between uncomplicated burn patients, complicated burn patients, and healthy controls.
- Analysis of cytokine concentrations and myeloperoxidase activity in wound exudates over time.
Main Results:
- Children with complicated burns exhibited significantly higher levels of multiple cytokines (IL-1RA, IL-6, IL-8, IL-10, TNF-α, IFN-γ, MCP-1, G-CSF) compared to uncomplicated burns and healthy children.
- Elevated levels of IL-6, IL-8, and MCP-1 were observed in uncomplicated burn patients.
- Wound exudates showed increased levels of IL-1β, IL-8, MCP-1, TNF-α, MIP-1α, and GM-CSF compared to plasma, suggesting the wound as a source of inflammation.
- Myeloperoxidase activity correlated with MIP-1α, TNF-α, and GM-CSF levels in wound exudates.
Conclusions:
- The severity of burn injury in children is associated with distinct systemic cytokine profiles.
- The burn wound acts as a significant source of inflammatory cytokines during active surgical treatment.
- Cytokines contribute to both local inflammation and systemic responses, influencing neutrophil activity in burn wounds.
Abstract:
The content of 27 cytokines was measured in blood plasma from 19 children with severe uncomplicated burns (group 1) and complicated burns (septic toxemia, toxemia, and pneumonia; group 2). Before surgical treatment (day 4 (+/-2) after burn), significant differences were found in the concentrations of interleukin-1 receptor antagonist, interleukin-6, interleukin-8, interleukin-10, tumor necrosis factor-alpha, interferon-gamma, MCP-1, and granulocyte colony-stimulating factor. Cytokine concentration in group 2 patients was much higher than in group 1 patients and healthy children. The concentrations of interleukin-6, interleukin-8, and MCP-1 in group 1 patients significantly surpassed the normal level. Cytokine concentration in the plasma and wound exudates and myeloperoxidase activity in wound exudates from 4 patients of group 2 were measured over 18 days after burn. The inflammatory response was characterized by an increase in the content of interleukin-1beta, interleukin-8, MCP-1, tumor necrosis factor-alpha, MIP-1alpha, and granulocyte-macrophage colony-stimulating factor in the wound (as compared to that in the plasma). Activity of myeloperoxidase in all patients was shown to correlate with the amount of MIP-1alpha (r=0.47), tumor necrosis factor-alpha (r=0.47), and granulocyte-macrophage colony-stimulating factor (r=0.55, p<0.05). Interleukin-8 concentration was beyond the limits of calibration. No correlation was found between the concentration of any of 27 cytokines in blood plasma and exudate. Our results indicate that during active surgical treatment, the wound serves as the source of inflammatory cytokines. Cytokines play a role in the systemic response and increase the degree of local inflammation, which modulates the number and activity of wound neutrophils.
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